The
HUMAN BRAIN during the
EARLY FIRST TRIMESTER
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The
HUMAN BRAIN during the
EARLY FIRST TRIMESTER
© 2008 by Taylor & Francis Group, LLC 1424_FM.indd 1
6/5/07 3:19:35 PM
ATLAS OF HUMAN CENTRAL NERVOUS SYSTEM DEVELOPMENT SERIES Shirley A. Bayer and Joseph Altman
VOLUME 1 The Spinal Cord from Gestational Week 4 to the 4th Postnatal Month
VOLUME 2 The Human Brain during the Third Trimester
VOLUME 3 The Human Brain during the Second Trimester
VOLUME 4 The Human Brain during the Late First Trimester
VOLUME 5 The Human Brain during the Early First Trimester
© 2008 by Taylor & Francis Group, LLC 1424_FM.indd 2
6/5/07 3:19:35 PM
The
HUMAN BRAIN during the
EARLY FIRST TRIMESTER
Shirley A. Bayer and Joseph Altman
Boca Raton London New York
CRC Press is an imprint of the Taylor & Francis Group, an informa business
© 2008 by Taylor & Francis Group, LLC 1424_FM.indd 3
6/5/07 3:19:35 PM
CRC Press Taylor & Francis Group 6000 Broken Sound Parkway NW, Suite 300 Boca Raton, FL 33487-2742 © 2008 by Taylor & Francis Group, LLC CRC Press is an imprint of Taylor & Francis Group, an Informa business No claim to original U.S. Government works Printed in the United States of America on acid-free paper 10 9 8 7 6 5 4 3 2 1 International Standard Book Number-13: 978-0-8493-1424-7 (Hardcover) This book contains information obtained from authentic and highly regarded sources. Reprinted material is quoted with permission, and sources are indicated. A wide variety of references are listed. Reasonable efforts have been made to publish reliable data and information, but the author and the publisher cannot assume responsibility for the validity of all materials or for the consequences of their use. No part of this book may be reprinted, reproduced, transmitted, or utilized in any form by any electronic, mechanical, or other means, now known or hereafter invented, including photocopying, microfilming, and recording, or in any information storage or retrieval system, without written permission from the publishers. For permission to photocopy or use material electronically from this work, please access www.copyright.com (http://www.copyright.com/) or contact the Copyright Clearance Center, Inc. (CCC) 222 Rosewood Drive, Danvers, MA 01923, 978-750-8400. CCC is a not-for-profit organization that provides licenses and registration for a variety of users. For organizations that have been granted a photocopy license by the CCC, a separate system of payment has been arranged. Trademark Notice: Product or corporate names may be trademarks or registered trademarks, and are used only for identification and explanation without intent to infringe. Visit the Taylor & Francis Web site at http://www.taylorandfrancis.com and the CRC Press Web site at http://www.crcpress.com
© 2008 by Taylor & Francis Group, LLC T&F_LOC_C_Master.indd 1424_FM.indd 4 1
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DEDICATION We dedicate this volume to the new generation of neuroscientists: those who use powerful molecular techniques to study the mechanisms of central nervous system (CNS) development, and those who use advanced scanning techniques to monitor the development of the CNS under normal and abnormal conditions.
ACKNOWLEDGMENTS We thank Dr. William DeMyer, pediatric neurologist at Indiana University Medical Center, for access to his personal library on human CNS development. We also thank the staff of the National Museum of Health and Medicine at the Armed Forces Institute of Pathology, Walter Reed Hospital, Washington, D.C.: Dr. Adrianne Noe, Director; Archibald J. Fobbs, Curator of the Yakovlev Collection; Elizabeth C. Lockett; and William Discher. We are most grateful to Dr. James M. Petras at the Walter Reed Institute of Research who made his darkroom facilities available so that we could develop all the photomicrographs on location rather than in our laboratory in Indiana. Finally, we thank Barbara Norwitz, Kari Budyk, and Suzanne Lassandro at CRC Press/Taylor & Francis for their personal attention to us and for expert help during production of the manuscript.
CONTENTS PART I. INTRODUCTION -------------------------------------------------------------------------------------------1 A. Organization of the Atlas ------------------------------------------------------------------------------1 B. Specimens -------------------------------------------------------------------------------------------------2 C. Photography and Computer Processing ------------------------------------------------------------2 D. Identification of Transient and Immature Brain Regions ---------------------------------------3 E. Major Developmental Features of the First Trimester Brain ----------------------------------3 PART II. GW7 CORONAL ---------------------------------------------------------------------------------------------4 Plates 1A, 1B (Level 1: Section 50) ----------------------------------------------------------------------6, 7 Plates 2A, 2B (Level 2: Section 116) --------------------------------------------------------------------8, 9 Plates 3A, 3B (Level 3: Section 164) -----------------------------------------------------------------10, 11 Plates 4A, 4B (Level 4: Section 201) -----------------------------------------------------------------12, 13 Plates 5A, 5B (Level 5: Section 242) -----------------------------------------------------------------14, 15 Plates 6A, 6B (Level 6: Section 283) -----------------------------------------------------------------16, 17 Plates 7A, 7B (Level 7: Section 325) -----------------------------------------------------------------18, 19 Plates 8A, 8B (Level 8: Section 375) -----------------------------------------------------------------20, 21 Plates 9A, 9B (Level 9: Section 410) -----------------------------------------------------------------22, 23 Plates 10A, 10B (Level 10: Section 424) -------------------------------------------------------------24, 25 Plates 11A, 11B (Level 11: Section 444) -------------------------------------------------------------26, 27 Plates 12A, 12B (Level 12: Section 500) -------------------------------------------------------------28, 29 Plates 13A, 13B (Level 13: Section 533) -------------------------------------------------------------30, 31 Plates 14A, 14B (Level 14: Section 572) -------------------------------------------------------------32, 33 Plates 15A, 15B (Level 15: Section 588) -------------------------------------------------------------34, 35 Plates 16A, 16B (Level 16: Section 628) -------------------------------------------------------------36, 37 Plates 17A, 17B (Level 17: Section 677) -------------------------------------------------------------38, 39 Plates 18A, 18B (Cerebral Cortex and Thalamus: Section 203) ----------------------------------40, 41 Plates 19A, 19B (Cerebral Cortex and Thalamus: Section 236) ----------------------------------42, 43 Plates 20A, 20B (Diencephalon and Mesencephalon: Section 390) ------------------------------44, 45 PART III. GW7 SAGITTAL ------------------------------------------------------------------------------------------- 46 Plates 21A, 21B (Level 1: Slide 13, Section 5) ------------------------------------------------------48, 49 Plates 22A, 22B (Level 2: Slide 12, Section 5) ------------------------------------------------------50, 51 Plates 23A, 23B (Level 3: Slide 11, Section 5) ------------------------------------------------------52, 53 Plates 24A, 24B (Level 4: Slide 9, Section 5) -------------------------------------------------------54, 55 Plates 25A, 25B (Level 5: Slide 8, Section 8) -------------------------------------------------------56, 57 Plates 26A, 26B (Level 6: Slide 8, Section 2) -------------------------------------------------------58, 59 Plates 27A, 27B (Level 7: Slide 6, Section 11) ------------------------------------------------------60, 61 Plates 28A, 28B (Pons/Medulla: Slides 9, 9, 8, Sections 5, 2, 8, respectively) -----------------62, 63 PART IV. GW7 HORIZONTAL ------------------------------------------------------------------------------------- 64 Plates 29A, 29B (Level 1: Section 9) ------------------------------------------------------------------66, 67 Plates 30A, 30B (Level 2: Section 29) ----------------------------------------------------------------68, 69 Plates 31A, 31B (Level 3: Section 36) ----------------------------------------------------------------70, 71 Plates 32A, 32B (Level 4: Section 39) ----------------------------------------------------------------72, 73 Plates 33A, 33B (Level 5: Section 45) ----------------------------------------------------------------74, 75 Plates 34A, 34B (Level 6: Section 50) ----------------------------------------------------------------76, 77 Plates 35A, 35B (Level 7: Section 55) ----------------------------------------------------------------78, 79 Plates 36A, 36B (Level 8: Section 65) ----------------------------------------------------------------80, 81 Plates 37A, 37B (Level 9: Section 71) ----------------------------------------------------------------82, 83 Plates 38A, 38B (Level 10: Section 87) --------------------------------------------------------------84, 85 Plates 39A, 39B (Level 11: Section 94) --------------------------------------------------------------86, 87 Plates 40A, 40B (Level 12: Section 112) -------------------------------------------------------------88, 89 Plates 41A, 41B (Level 13: Section 118) -------------------------------------------------------------90, 91 Plates 42A, 42B (Level 14: Section 141) -------------------------------------------------------------92, 93
CONTENTS Plates 43A, 43B (Level 15: Section 152) -------------------------------------------------------------94, 95 Plates 44A, 44B (Level 16: Section 169) -------------------------------------------------------------96, 97 Plates 45A, 45B (Level 17: Section 205) -------------------------------------------------------------98, 99 PART V. GW6.5 CORONAL ---------------------------------------------------------------------------------------100 Plates 46A, 46B (Level 1: Sections 66) ------------------------------------------------------------102, 103 Plates 47A, 47B (Level 2: Sections 107) ----------------------------------------------------------104, 105 Plates 48A, 48B (Level 3: Section 130) -----------------------------------------------------------106, 107 Plates 49A, 49B (Level 4: Section 159) -----------------------------------------------------------108, 109 Plates 50A, 50B (Level 5: Section 190) -----------------------------------------------------------110, 111 Plates 51A, 51B (Level 6: Section 241) -----------------------------------------------------------112, 113 Plates 52A, 52B (Level 7: Section 258) -----------------------------------------------------------114, 115 Plates 53A, 53B (Level 8: Section 285) -----------------------------------------------------------116, 117 Plates 54A, 54B (Level 9: Section 330) -----------------------------------------------------------118, 119 Plates 55A, 55B (Level 10: Section 357) ----------------------------------------------------------120, 121 Plates 56A-56B (Level 11: Section 384) ----------------------------------------------------------122, 123 Plates 57A, 57B (Level 12: Section 420) ----------------------------------------------------------124, 125 Plates 58A, 58B (Level 13: Section 438) ----------------------------------------------------------126, 127 Plates 59A, 59B (Level 14: Section 488) ----------------------------------------------------------128, 129 Plates 60A, 60B (Level 15: Section 553) ----------------------------------------------------------130, 131 Plates 61A, 61B (Level 16: Section 583) ----------------------------------------------------------132, 133 Plates 63A, 63B (Cerebral Cortex, Future Paracentral Lobule: Section 643) ----------------136, 137 PART VI. GW6.5 SAGITTAL ---------------------------------------------------------------------------------------138 Plates 64A, 64B (Level 1: Slide 27, Section 14) --------------------------------------------------140, 141 Plates 65A, 65B (Level 2: Slide 25, Section 9) ---------------------------------------------------142, 143 Plates 66A, 66B (Level 3: Slide 23, Section 8) ---------------------------------------------------144, 145 Plates 67A, 67B (Level 4: Slide 21, Section 2) ---------------------------------------------------146, 147 Plates 68A, 68B (Level 5: Slide 19, Section 8) ---------------------------------------------------148, 149 Plates 69A, 69B (Level 6: Slide 18, Section 8) ---------------------------------------------------150, 151 Plates 70A, 70B (Level 7: Slide 16, Section 8) ---------------------------------------------------152, 153 Plates 71A, 71B (Dorsal Neocortex: Slide 23, Section 8) ---------------------------------------154, 155 Plates 72A, 72B (Hippocampus and Thalamus: Slide 26, Section 9) -------------------------156, 157 Plates 73A, 73B (Hypothalamus: Slide 27, Section 14) -----------------------------------------158, 159 Plates 74A, 74B (Mesencephalic Tegmentum: Slides 27, 21, Sections 7. 8. respectively) --------------------------------------------------------- 160-161 Plates 75A, 75B (Mesencephalic Tectum, Isthmus, and Cerebellum: Slide 24, Section 8) --------------------------------------------------------------162, 163 Plates 76A, 76B (Cerebellum: Slides 27, 18, Sections 14, 5, respectively) ------------------164, 165 Plates 77A, 77B (Trigeminal Nerve Entry Zone: Slide 19, Section 3) ------------------------166, 167 Plates 78A, 78B (Lateral Cerebellum, Pons, and Medulla: Slide 16, Section 3) -------------168, 169 Plates 79A, 79B (Trigeminal and Vestibulo-Cochlear Nerve Entry Zones: Slide 16, Section 13) -----------------------------------------------------------------170, 171 Plates 80A, 80B (Entry Zones of Nerves IX and X: Slide 18, Section 13) -------------------172, 173 Plates 81A, 81B (Medial Pons and Medulla: Slide 21, Section 8) -----------------------------174, 175 Plates 82A, 82B (Neuroepithelium and Midline Raphe Glial Structure [Isthmus and Upper Pons]: Slide 27, Section 14) ------------------------------------------------176, 177 Plates 83A, 83B (Neuroepithelium and Midline Raphe Glial Structure [Near Pontine Flexure]: Slide 27, Section 14) ---------------------------------------------------178, 179 Plates 84A, 84B (Neuroepithelium and Midline Raphe Glial Structure [Near Medullary Flexure]: Slide 27, Section 14) ------------------------------------------------180, 181 PART VII. GW5.5 CORONAL ---------------------------------------------------------------------------------------182 Plates 85A, 85B (Level 1: Section 29) -------------------------------------------------------------184, 185
CONTENTS Plates 86A, 86B (Level 2: Section 42) -------------------------------------------------------------186, 187 Plates 87A, 87B (Level 3: Section 100) -----------------------------------------------------------188, 189 Plates 88A, 88B (Level 4: Section 128) -----------------------------------------------------------190, 191 Plates 89A, 89B (Level 5: Section 169) -----------------------------------------------------------192, 193 Plates 90A, 90B (Level 6: Section 192) -----------------------------------------------------------194, 195 Plates 91A, 91B (Level 7: Section 215) -----------------------------------------------------------196, 197 Plates 92A, 92B (Level 8: Section 237) -----------------------------------------------------------198, 199 Plates 93A, 93B (Level 9: Section 255) -----------------------------------------------------------200, 201 Plates 94A, 94B (Level 10: Section 269) ----------------------------------------------------------202, 203 Plates 95A, 95B (Level 11: Section 285) ----------------------------------------------------------204, 205 Plates 96A, 96B (Level 12: Section 308) ----------------------------------------------------------206, 207 Plates 97A, 97B (Level 13: Section 334) ----------------------------------------------------------208, 209 Plates 98A, 98B (Level 14: Section 376) ----------------------------------------------------------210, 211 Plates 99A, 99B (Telencephalon and Diencephalon: Sections 85, 83, 123) ------------------212, 213 PART VIII. GW5.5 SAGITTAL ---------------------------------------------------------------------------------------214 Plates 100A, 100B (Level 1: Slide 11, Section 6) -------------------------------------------------216, 217 Plates 101A, 101B (Level 2: Slide 9, Section 14) ------------------------------------------------218, 219 Plates 102A, 102B (Level 3: Slide 8, Section 14) ------------------------------------------------220, 221 Plates 103A, 103B (Level 4: Slide 7, Section 10) ------------------------------------------------222, 223 Plates 104A, 104B (Level 5: Slide 6, Section 15) ------------------------------------------------224, 225 Plates 105A, 105B (Dorsal Cerebral Cortex: Slide 18, Section 8) -----------------------------226, 227 Plates 106A, 106B (Basal Telencephalon: Slide 11, Section 6) --------------------------------228, 229 Plates 107A, 107B (Septum and Diencephalon: Slide 11, Section 6) -------------------------230, 231 Plates 108A, 109B (Midbrain Tegmentum: Slide 11, Section 6) -------------------------------232, 233 Plates 109A, 109B (Isthmus and Cerebellum: Slide 11, Section 6) ---------------------------234, 235 Plates 110A, 111A, 110B. 111B (Pons and Medulla: Slide 8, Section 10) ------------------- 236-239 Plates 112A, 112B (Rhombencephalon: Slide 7, Section 6) ------------------------------------240, 241 Plates 113A, 114A, 113B, 114B (Rhombencephalon: Slide 6, Section 11) ------------------ 242-245 PART IX. GW5 CORONAL ------------------------------------------------------------------------------------------246 Plates 115A, 115B (Levels 1-2: Sections 12, 42) ------------------------------------------------248, 249 Plates 116A, 116B (Level 3: Section 82) ----------------------------------------------------------250, 251 Plates 117A, 117B (Level 4: Section 97) ----------------------------------------------------------252, 253 Plates 118A, 118B (Level 5: Section 117) --------------------------------------------------------254, 255 Plates 119A, 119B (Level 6: Section 127) --------------------------------------------------------256, 257 Plates 120A, 120B (Level 7: Section 162) --------------------------------------------------------258, 259 Plates 121A, 121B (Level 8: Section 172) --------------------------------------------------------260, 261 Plates 122A, 122B (Level 9: Section 182) --------------------------------------------------------262, 263 Plates 123A, 123B (Level 10: Section 192) -------------------------------------------------------264, 265 Plates 124A, 124B (Level 11: Section 222) -------------------------------------------------------266, 267 PART X. GW5 SAGITTAL -------------------------------------------------------------------------------------------268 Plates 125A, 125B (Level 1: Slide 6, Section 2) --------------------------------------------------270, 271 Plates 126A, 126B (Level 2: Slide 5, Section 2) -------------------------------------------------272, 273 Plates 127A, 127B (Level 3: Slide 4, Section 7) -------------------------------------------------274, 275 Plates 128A, 128B (Level 4: Slide 3, Section 24) ------------------------------------------------276, 277 Plates 129A, 129B (Level 5: Slide 3, Section 12) ------------------------------------------------278, 279 Plates 130A, 130B (Level 6: Slide 3, Section 5) -------------------------------------------------280, 281 Plates 131A, 131B (Level 7: Slide 2, Section 22) ------------------------------------------------282, 283 Plates 132A, 132B (Hypothalamus, Mesencephalon, and Rhombencephalon: Slide 5, Section 22) -----------------------------------------------------------284, 285 Plates 133A, 133B (Cerebellum and Pons: Slide 3, Section 24) -------------------------------286, 287
CONTENTS PART XI. GW4.5 CORONAL ---------------------------------------------------------------------------------------288 Plates 134A, 134B (Levels 1-2: Sections 5, 35) --------------------------------------------------290, 291 Plates 135A, 135B (Level 3: Section 65) ----------------------------------------------------------292, 293 Plates 136A, 136B (Level 4: Section 75) ----------------------------------------------------------294, 295 Plates 137A, 137B (Level 5: Section 85) ----------------------------------------------------------296, 297 Plates 138A, 138B (Level 6: Section 95) ----------------------------------------------------------298, 299 Plates 139A, 139B (Level 7: Section 115) --------------------------------------------------------300, 301 Plates 140A, 140B (Level 8: Section 135) --------------------------------------------------------302, 303 Plates 141A, 141B (Level 9: Section 145) --------------------------------------------------------304, 305 Plates 142A, 142B (Level 10: Section 155) -------------------------------------------------------306, 307 Plates 143A, 143B (Level 11: Section 165) -------------------------------------------------------308, 309 Plates 144A, 144B (Level 12: Section 185) -------------------------------------------------------310, 311 Plates 145A, 145B (Level 13: Section 200) -------------------------------------------------------312, 313 Plates 146A, 146B (Level 12: Section 210) -------------------------------------------------------314, 315 PART XII. GW4 SAGITTAL ------------------------------------------------------------------------------------------316 Plates 147A, 147B (Level 1: Slide 4, Section 32) -------------------------------------------------318, 319 Plates 148A, 148B (Level 2: Slide 4, Section 24) ------------------------------------------------320, 321 Plates 149A, 149B (Level 3: Slide 4, Section 16) ------------------------------------------------322, 323 Plates 150A, 150B (Level 4: Slide 4, Section 8) -------------------------------------------------324, 325 Plates 151A, 151B (Level 5: Slide 3, Section 40) ------------------------------------------------326, 327 Plates 152A, 152B (Level 6: Slide 3, Section 32) ------------------------------------------------328, 329 Plates 153A, 153B (Level 7: Slide 3, Section 24) ------------------------------------------------330, 331 Plates 154A, 154B (Level 8: Slide 3, Section 16) ------------------------------------------------332, 333 Plates 155A, 155B (Level 9: Slide 3, Section 8) -------------------------------------------------334, 335 Plates 156A, 156B (Subdivisions of the Prosencephalic Neuroepithelium: Slide 4, Section 24) -------------------------------------------------------------336, 337 Plates 157A, 157B (Isthmus, Cerebellum, and Pons: Slide 4, Section 24) -------------------338, 339 Plates 158A, 158B (Rhombomeres in Pons and Medulla: Slide 3, Section 40) --------------340, 341 Plates 159A, 159B (Rhombencephalon and Sensory Cranial Nerve Entry Zones: Slide 3, Section 24) ----------------------------------------------------------342, 343 Plates 160A, 160B (Midline Raphe Glial Structure: Slide 4, Section 24) --------------------344, 345 PART XIII. GW4 CORONAL ------------------------------------------------------------------------------------------346 Plates 161A, 161B (Levels 1-2: Sections 9, 27) --------------------------------------------------348, 349 Plates 162A, 162B (Level 3: Section 36) ----------------------------------------------------------350, 351 Plates 163A, 163B (Level 4: Section 48) ----------------------------------------------------------352, 353 Plates 164A, 164B (Level 5: Section 63) ----------------------------------------------------------354, 355 Plates 165A, 165B (Level 6: Section 72) ----------------------------------------------------------356, 357 Plates 166A, 166B (Level 7: Section 75) ----------------------------------------------------------358, 359 Plates 167A, 167B (Level 8: Section 81) ----------------------------------------------------------360, 361 Plates 168A, 168B (Level 9: Section 84) ----------------------------------------------------------362, 363 Plates 169A, 169B (Level 10: Section 90) --------------------------------------------------------364, 365 Plates 170A, 170B (Level 11: Section 93) --------------------------------------------------------366, 367 Plates 171A, 171B (Level 12: Section 99) --------------------------------------------------------368, 369 PART XIV. GW3.8 SAGITTAL ---------------------------------------------------------------------------------------370 Plates 172A, 172B (Level 1: Slide 2, Section 30) -------------------------------------------------372, 373 Plates 173A, 173B (Level 2: Slide 2, Section 24) ------------------------------------------------374, 375 Plates 174A, 174B (Level 3: Slide 2, Section 20) ------------------------------------------------376, 377 Plates 175A, 175B (Level 4: Slide 2, Section 16) ------------------------------------------------378, 379 Plates 176A, 176B (Level 5: Slide 2, Section 12) ------------------------------------------------380, 381 Plates 177A, 177B (Level 6: Slide 2, Section 8) -------------------------------------------------382, 383 Plates 178A, 178B (Level 7: Slide 1, Section 38) ------------------------------------------------384, 385
CONTENTS Plates 179A, 179B (Level 8: Slide 1, Section 30) ------------------------------------------------386, 387 Plates 180A-182A, 180B-182B (Prosencephalon, Mesencephalon, and Anterior Rhombencephalon: Slide 2, Sections 33, 24, and 20 respectively) ---------------------------- 388-393 Plates 183A, 183B (Lateral Mesencephalon and Rhombencephalon: Slide 2, Section 12) 394, 395 Plates 184A, 184B (Lateral Prosencephalon, Mesencephalon, and Rhombencephalon: Slide 2, Section 42) -----------------------------------------------------------------------------------396, 397 PART XV. GW3.2 CORONAL ---------------------------------------------------------------------------------------398 Plates 185A, 185B (Levels 1-2: Sections 3, 13) --------------------------------------------------400, 401 Plates 186A, 186B (Level 3: Section 18) ----------------------------------------------------------402, 403 Plates 187A, 187B (Level 4: Section 28) ----------------------------------------------------------404, 405 Plates 188A, 188B (Level 5: Section 33) ----------------------------------------------------------406, 407 Plates 189A, 189B (Level 6: Section 38) ----------------------------------------------------------408, 409 Plates 190A, 190B (Level 7: Section 43) ----------------------------------------------------------410, 411 Plates 191A, 191B (Level 8: Section 58) ----------------------------------------------------------412, 413 Plates 192A, 192B (Level 9: Section 63) ----------------------------------------------------------414, 415 Plates 193A, 193B (Level 10: Section 68) --------------------------------------------------------416, 417 Plates 194A, 194B (Level 11: Section 73) --------------------------------------------------------418, 419 Plates 195A, 195B (Level 12: Section 78) --------------------------------------------------------420, 421 Plates 196A, 196B (Level 13: Section 83) --------------------------------------------------------422, 423 Plates 197A, 197B (Levels 14-15: Sections 88, 93) ---------------------------------------------424, 425 PART XVI. CONCLUDING ESSAY ---------------------------------------------------------------------------------426 A. Overview -----------------------------------------------------------------------------------------------426 B. The NEP Matrix: Stockbuilding NEP Cells and Differentiating NEP Cells --------------428 C. The Superventricles and the Superarachnoid Reticulum ------------------------------------430 D. Metamerism or Mosaicism as Principles of CNS Development -----------------------------441 E. Exogenous and Endogenous Mechanisms of NEP Cell Diversification --------------------447 F. Timespans of Neurogenesis -------------------------------------------------------------------------465 G. Cell Migration, Sojourn Zones, Secondary Germinal Matrices, and Fate-Restricted Glioepithelia ------------------------------------------------------------------466 H. Centro-Central Signaling and the Morphogenetic Maturation of the CNS----------------482 I. Summary: The Epochs, Phases, and Mechanisms of CNS Development -------------------484 J. A Note on the Functional Maturation of the Human CNS ------------------------------------485 APPENDIX Timespans of Neurogenesis ------------------------------------------------------------------------------490 REFERENCES ------------------------------------------------------------------------------------------------------------------498 GLOSSARY
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1
PART PARTII
INTRODUCTION INTRODUCTION A. Organization of the Atlas This is the last volume in the Atlas of Human Central Nervous System Development series. It deals with human brain development during the early first trimester from the 3rd through the 7th gestational weeks (GW3-GW7). Volume 1 (Bayer and Altman, 2002) records the development of the spinal cord from GW4 to the 4th postnatal month. Volumes 2 through 5 deal with prenatal brain development. The analysis procedes in reverse (older-toyounger) order: from more recognizable brain structures in the third trimester to progressively less familiar structures in the second trimester to often uncertain or hypothetical structures in the first trimester. Volume 2 (Bayer and Altman, 2004a) records brain development during the third trimester, with specimens ranging in age from GW37 to GW26; its major theme is the maturation of the brain’s settled and enduring neuron populations. Volume 3 (Bayer and Altman, 2005) deals with brain development during the second trimester, with specimens ranging in age from GW24 to GW13.5; its major theme is the migration, sojourning, and settling of the brain’s diverse neuron populations. Volume 4 (Bayer and Altman, 2006) presents brain development during the late first trimester, with specimens ranging in age from GW11 to GW7.5; its major theme is the neuroepithelial mosaics that generate different populations of neurons and glia. This volume presents brain development during the early first trimester, with specimens ranging in age from GW7.0 to GW3.2, and has four major themes: (1) growth of the stockbuilding neuroepithelium along the expanding shorelines of the brain’s superventricles, (2) early neurogenesis, (3) the onset of brain parenchymal development related to the expansion and decline of the superarachnoid reticulum, and (4) the inductive and signaling interactions between the brain and peripheral structures in the skull. The present volume features 14 normal specimens. Approximately two specimens near the same age were selected for analysis, one cut in the transverse (mainly coronal) plane, the other cut in the sagittal plane. For the oldest age group (GW7), there is a third specimen sectioned mainly in the horizontal plane. (Younger horizontally sectioned specimens are not in any of the collections we examined.) Each specimen is presented as a series of grayscale photographs of its Nissl-stained brain sections
including the surrounding skull (Parts II through XV). The photographs are shown from anterior to posterior (coronal specimens), medial to lateral (sagittal specimens), and dorsal to ventral (horizontal GW7 specimen). Portrait orientation is used for the coronal specimens; the dorsal part of each section is toward the top of the page, the ventral part at the bottom, and the midline is in the vertical center of each section. Landscape orientation is used for the horizontal specimen; the anterior part of each section is facing to the left (bottom of page), posterior to the right (top of page), and the midline is in the horizontal center of each section. All coronal and horizontal specimes have computer-aided 3-dimensional reconstructions of their brains showing each section’s location. That reconstruction clears up the ambiguity about the exact plane of sectioning through each brain; a problem we addressed in Volume 4. Portrait orientation is used for all sagittal specimens; the anterior part of each section is facing left, posterior right, dorsal top, and ventral bottom. Parts II through XV contain companion plates, designated as A and B on facing pages. Part A on the left page shows the full contrast photograph with labels of the skull and peripheral neural structures; part B on the right page shows low contrast copies of the same photograph with superimposed outlines of the labeled brain parts. The low magnification plates show entire sections to identify the large structures and subdivisions of the brain. The high magnification plates feature enlarged views of the brain core to identify smaller structures. For ease of interpretation in all plates, the ventricles are labeled in capitals, the neuroepithelium and other germinal zones in Helvetica bold, transient structures in Times bold italic, and permanent structures in Times Roman or Times bold. Fixation artifacts are usually outlined with dashed lines in part B of each plate, but few specimens in this volume have artifacts. Since this is the final volume in the series, a Concluding Essay (Part XVI) links major themes of brain development at the cell and tissue level (described in the Atlas Series) with current neuro-developmental studies on gene expression and other molecular markers. Figure 15 to Figure 43 in the essay bring together photographs of individual brain structures at various ages so that the sequence of development is immediately apparent. An Appendix contains tables listing the estimated timespans of neurogenesis for the major populations in the human central ner-
2 vous system (CNS) based on experimentally determined data in rats. References follow the appendix, and the Atlas concludes with an alphabetized Glossary that defines the developmental structures labeled in the plates.
B. Specimens All specimens are from the collections of human embryos and fetal brains currently kept at the National Museum of Health and Medicine, Armed Forces Institute of Pathology, Washington, D.C. Nine specimens are from the Carnegie Collection and are designated by their respective numbers with the prefix C. The Carnegie Collection was started by Franklin P. Mall (1862-1917) and expanded at the Carnegie Institution of Washington under the direction of George L. Streeter (1873-1948) and George W. Corner (1889-1981). Five specimens are from the Minot Collection and are designated by their respective numbers with the prefix M. The Minot Collection is named after Charles S. Minot (1852-1914), who collected and prepared over 1900 embryos of different animal species, and approximately 100 human embryos, close to a century ago.
C. Photography and Computer Processing All specimens were photographed using either an Olympus photomicroscope or a Wild photomakroskop. The magnification varied for each specimen according to the size of the head; the section with the largest area that could be accommodated within the field of view set the magnification for all sections of a particular specimen. All photographs were taken with a green filter to increase the contrast of the black and white film (Kodak technical pan #TP442). The film was developed at 20°C for 6 to 7 min in Kodak HC110 developer (dilution F), followed by Kodak stop bath for 30 s, Kodak fixer for 5 min, Kodak hypo clearing agent for 1 min, running water rinse for 10 min, and a brief rinse in Kodak photoflo before drying. The negatives were scanned at 2700 dots-per-inch (dpi) with a Nikon Coolscan-1000 35-mm film scanner, which was interfaced to a PowerPC G3 Macintosh computer running Adobe Photoshop with a plug-in Nikon driver. To capture the subtle shades of gray, the negatives were scanned as color positives, inverted, and converted to grayscale. Using the enhancement features built into Adobe Photoshop and the additional features of Extensis Intellihance, adjustments were made to increase contrast and sharpness. When the image resolution was set to 300 dpi, a full-size photographic file printed at approximately 12 to 10 in. Most images are shown at slightly reduced full size on separate pages. Adobe Illustrator was used to superimpose labels and to outline structural details on low contrast copies of the Adobe Photoshop files. The plates were placed into a book-form layout using Adobe InDesign. Finally, camera-ready files were provided to Taylor & Francis in Adobe portable document format (pdf).
The entire brain and upper cervical spinal cord of each transversely cut specimen was three-dimensionally reconstructed in five steps. First, photographs of serial sections were made throughout the entire brain; the negatives were scanned and converted to computer files as described in the preceding paragraph. Second, all the files of sections selected for the reconstruction were placed into one large Photoshop file that contained a separate photograph in each layer. By altering the visibility and transparency of these layers the sections were aligned to each other as they were before sectioning. Then each layer was saved as a separate file. Third, Adobe Illustrator was used to outline the brain surface of each aligned section, and these contours were saved in separate Adobe Illustrator encapsulated postscript (eps) files. Fourth, the eps files were imported into 3D space (x, y, and z coordinates) using Cinema 4DXL (C4D, Maxon Computer, Inc.). For each section, points on the contours have unique x-y coordinates and the same z coordinate. By calculating the distance between sections, the entire array of contours was stretched out in the z axis. The C4D loft tool builds a “skin” of the brain as a spline mesh of polygons. The polygons start from the x-y points on the first contour with the most anterior z coordinate, to the x-y points on the next contour behind it, and finish with the x-y points on the last contour with the most posterior z coordinate. The spline meshes of the entire brain surface were rendered at various camera angles as completely opaque using the C4D ray-tracing engine. These reconstructions are shown in Figure 1 to Figure 14. Fifth, spline meshes of the brain surface posterior to a specific section (coronal brains) or ventral to a specific section (horizontal brain) were rendered with a copy of the photograph of the particular section texture-mapped as a cap on the model. These reconstructions are shown as insets in Part A of each low magnification plate of the coronal and horizontal specimens.
D. Identification of Transient and Immature Brain Regions With the exception of the rhombomeres in the pons and medulla that are visible prior to and including GW5.5, the identification of most structures in early first trimester human brain—in particular, the various neuroepithelial (NEP) compartments—have received little attention in the past. Most identifications are based on our previous 3H-thymidine autoradiographic work with rats. There is a great similarity between the rat brain and human brain in the sequential order of neurogenesis and early neuronal differentiation, especially in the brainstem. Our experimental studies in the rat and the rationale for most of the proven or putative identifications we make are in the following publications. Amygdala: Bayer (1980c). Basal Ganglia: Bayer (1984, 1985b, 1987). Cerebellum: Altman and Bayer (1978a, 1982a, 1985a,
3 1985b, 1985c, 1997). Cerebral Cortex: Altman and Bayer (1990a, 1990b); Bayer and Altman (1990, 1991a). Cranial Nerve Nuclei: Altman and Bayer (1980a, 1980b, 1980c, 1982b). Hippocampus: Altman (1963); Altman and Das (1965a); Altman and Bayer (1975, 1990c, 1990d, 1990e); Bayer (1980a, 1980b). Hypothalamus: Altman and Bayer (1978c, 1978d, 1978e, 1986). Medulla: Altman and Bayer (1978b, 1980a, 1980b, 1980c, 1982b). Midbrain: Altman and Bayer (1981a, 1981b, 1981c). Olfactory Bulb: Altman (1969); Bayer (1983). Pontine Area: Altman and Bayer (1978b, 1980d, 1987a, 1987b, 1987c, 1987d). Precerebellar Nuclei: Altman and Bayer (1978b, 1987a, 1987b, 1987c, 1987d, 1997). Preoptic Area: Altman and Bayer (1986); Bayer and Altman (1987). Rhinencephalon: Bayer (1985a, 1986a, 1986b); Bayer and Altman (1991b). Septal Area: Bayer (1979a, 1979b). Spinal Cord: Altman and Bayer (1984, 2001). Thalamus: Altman and Bayer (1979a, 1979b, 1979c, 1988a, 1988b, 1988c, 1989a, 1989b, 1989c).
E. Major Developmental Features of the First Trimester Brain In Part XVI, Concluding Essay, we summarize the landmark events that characterize the development of the human CNS during the first trimester. Briefly reviewed, they are the following. (i) For several weeks after closure of the neural tube (the future spinal cord) and the neural vesicles (the future rhombencephalon, mesencephalon, diencephalon, and telencephalon), the CNS consists of a single proliferative tissue, the stockbuilding neuroepithelium (NEP). These NEP cells do not produce neurons and neuroglia but rather the growing stock of pluripotent progenitor cells that will later give rise to the differentiating cells of the CNS. (ii) The proliferating NEP cells undergo mitosis near the lumen of the ventricles, hence the growth of the stockbuilding NEP matrix is associated with the expansion of the narrow protoventricles to produce the large rhombencephalic, mesencephalic, diencephalic, and telencephalic superventricles.
(iii) The rate of stockbuilding cell mitosis varies in different components of the NEP matrix in relation to the sizes of the neuronal populations being generated for different brain structures. This results in a variegated ventricular shoreline (rhombomeres, evaginations, invaginations, eminences). We refer to these distinguishable NEP matrix shorelines as NEP cell mosaics. (iv) When NEP cell proliferation shifts from stockbuilding progenitor cells to unloading postmitotic neurons and neuroglia, these cells migrate outward and accumulate in the brain parenchyma, the space situated between the NEP and the pia. We present evidence that the formation of a hitherto unidentified meningeal structure, the superarachnoid reticulum, is related to this parenchymal expansion. The superarachnoid reticulum is a broad, fluid-rich meningeal tissue sandwiched between the early-developing pia and the formative dura. The initial expansion of the superarachnoid reticulum antedates the appearance of the brain parenchyma. While the parenchyma continually expands as more and more neurons migrate into it and differentiate, the superarachnoid reticulum continually shrinks until it is a thin meninx. We postulate that the transient hypertophy of the superarachnoid reticulum serves as a parenchymal expansion field for the developing brain. (v) The shrinkage of the NEP matrix is coupled with cell migration. A small complement of migrating cells produce fate-restricted secondary germinal matrices away from the ventricle, such as the external germinal layer of the cerebellum and the subgranular zone of the hippocampus. The bulk of migrating cells are young neurons that may sojourn in transitional fields but eventually settle in their final locations throughout the parenchyma. (vi) Peripheral and central inductive and signaling mechanisms play a major role in producing fate-restricted NEP cell mosaics, guiding migrating neurons, and directing axons to grow to their targets. Interactions between the NEP and the cephalic and branchial placodes (peripherocentral signaling) influence the diversification of NEP mosaics. Centro-central signaling between CNS structures is responsible for the coordinated development of different brain regions not directly connected with the periphery. (vii) An attempt is made to relate the morphological evidence for NEP matrix diversification, cell-fate restriction, neuronal migration, and axonal guidance in the human CNS with the underlying genetic and molecular mechanisms revealed by current research in animals.
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PART PARTII: II: GW7 GW7 CORONAL CORONAL This specimen is embryo #2155 in the Minot Collection, designated here as M2155. The crown-rump length (CR) is 17.5 mm estimated to be at gestational week (GW) 7. Most of M2155’s brain sections are cut (10 µm) in the coronal plane, but the plane shifts to predominantly horizontal in the posterior medulla. We photographed 71 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and cerebellum. Seventeen of these sections are illustrated in Plates 1AB to 17AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of M2155’s brain (Figure 1), and to show each illustrated section in situ (insets, Plates 1A-17A). A prominent developmental strategy during the early first trimester is that many developing brain structures interact with primordial structures in the head and neck. Consequently, each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify nonneural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. Plates 18-20 show high-magnification views of the cerebral cortex, diencephalon, and mesencephalon. Some highmagnification plates are rotated 90˚ (landscape orientation) to more efficiently use page space. The brain of M2155 has considerable variation in the thickness of the neuroepithelium and in the number of migrating neurons in various parts of the brain parenchyma. Throughout the telencephalon, the neuroepithelium is the most prominent structure surrounding the enlarging telencephalic superventricle. A cell-sparse primordial plexiform layer is adjacent to the cerebral cortical neuroepithelium. A few pioneer Cajal-Retzius neurons have migrated into this layer, but most cortical neurons have not yet been generated. The cerebral cortical neuroepithelium is growing by adding more neuonal stem cells that will produce neurons during the late first trimester (Volume 4, Bayer and Altman, 2006) and early second trimester (Volume 3, Bayer and Altman, 2005). In contrast to the cerebral cortical neuroepithelium, the basal ganglionic and basal telencephalic neuroepithelia do have adjacent migrating neurons. In some areas, these neurons appear to migrate together in early (outermost and less dense) to late (innermost and most dense) waves. In accordance with the peripheral interaction theme, there is only the slightest indication of an olfactory bulb evagination in spite of the fact that a fully invaginated olfactory epithelium is in the nasal cavity and olfactory nerve fibers already contact the brain just anterior to the basal telencephalon. We hypothesize that olfactory nerve fibers have the capacity to induce the cortical neuroepithelium to proliferate and evaginate into an olfactory bulb later on. There is an olfactory evagi-
nation by GW7.5 (See Volume 4, Bayer and Altman, 2006, Plates 188A and B, pp. 464-465). The diencephalic neuroepithelium surrounds a slit-like superventricle. It is thinnest in the hypothalamic and subthalamic areas, where it is surrounded by densely packed waves of migrating neurons. It is postulated that these areas of the superventricle have shrinking shorelines as the neuroepithelia “unload” their stock of neuronal precursors. In contrast, the superventricle shoreline is still expanding as the thalamic neuroepithelium continues to add more neuronal precursors than to unload postmitotic neurons. The few neurons outside the thalamic neuroepithelium are postulated to be the oldest neurons in the ventral complex, posterior complex, and the reticular nucleus. The mesencephalon contains a stockbuilding neuroepithelium in the pretectum and tectum (relatively few adjacent migrating neurons). On the other hand, the tegmental and isthmal neuroepithelia are much thinner because most of their neuronal progeny has migrated out. These cells accumulate as inner dense clumps and outer sparse arrays interspersed among the thick accumulations of subpial fiber bands in the tegmental and isthmal parenchyma. Both the pons and medulla have neuroepithelia that are shrinking as they have already unloaded their neuronal precursors into an expanding parenchyma. Cells are migrating and settling in longitudinal arrays at the pontine flexure. A few cells are settling in the superior olive complex and many are settling in the reticular formation throughout the pons and medulla. Facial motor neurons are migrating from medial to lateral, leaving behind their axons in the genu of the facial nerve. Migrating cochlear nuclear neurons are outside the neuroepithelium in the anterior part of the lower rhombic lip, while migrating inferior olive neurons are in the posterior intramural migratory stream outside the precerebellar neuroepithelium in the posterior lower rhombic lip; some neurons have already settled in the inferior olive. Many neurons have settled in the solitary nucleus, surrounding a definite solitary tract. The hypoglossal nucleus is also distinguishable in the lower medulla. The cerebellar neuroepithelium is exceptional in the rhombencephalon because it is the only neuroepithelium still in the stockbuilding phase, mainly adding precursors of Purkinje cells. Many deep nuclear neurons have already been generated and are migrating in the cellular layers of the cerebellar transitional field. The fibrous layers probably contain afferents from the spinal cord and the vestibular ganglion.
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M2155 Computer-aided 3-D Brain Reconstructions Pineal evagination
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Inferior colliculus
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Infundibulum
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Invagination of choroid plexus into fourth ventricle
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Lower rhombic lip
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Medullary velum (covers 4th ventricle)
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BRAINSTEM FLEXURES
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Optic evagination
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Optic evagination
Lower rhombic lip
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Olfactory evagination
Side view
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P o ns
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Figure 1. A, The left side of the 3-D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following o r Plates. l u s B, a straight view of the left side. C, a straight down view of the top. D, an upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
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Olfactory evagination
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PLATE 1A GW7 Coronal CR 17.5 mm M2155 Level 1: Section 50 Non-neural structures labeled Branches of anterior cerebral artery in pial vascular network
Superior sagittal sinus (in interhemispheric fissure) Dural vascular network
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Future skin and skull (cell dense) Future dura (cell dense internal border of skull) Superarachnoid reticulum (cell sparse) Pia
Branches of middle cerebral artery Superarachnoid reticulum (cell sparse) Future frontal bone Frontonasal process Nasal septum Lateral nasal process
Nostril
Level 1: Computer-aided 3-D Brain Reconstruction
Medial nasal process
The GW7 Face and Neck
Figure 247E modified (Patten, 1953, p. 429.)
Nasal septum Medial nasal process
Frontal prominence Frontonasal process Eye
Lateral nasal process Nostril Mouth
Maxilla Mandible External ear Hyoid bone Laryngeal cartilages
7
PLATE 1B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Neural structures labeled Interhemispheric fissure
TELENCEPHALON CEREBRAL CORTEX
Brain surface (heavier line)
Neocortical NEP
Dural outline is external border of superarachnoid reticulum Cortical primordial plexiform layer
telencephalic superventricle
anterodorsal pool
Limbic cortical NEP
(future lateral ventricle)
Migrating Cajal-Retzius cells and subplate neurons
Cingulate
Limbic cortical (insular) NEP
Prefrontal? anteroventral pool
Basal ganglionic (anterolateral) NEP?
Migrating basal ganglionic neurons?
BASAL GANGLIA Migrating Cajal-Retzius cells and subplate neurons
Earlier maturation is indicated by the presence of migrating neurons outside the basal ganglionic, insular, and prefrontal NEPs. Later maturation is indicated by the absence of migrating neurons outside the neocortical and cingulate NEPs.
Major Arteries at Base of Brain
Figure 394D modified (Patten, 1953, p. 625.) Anterior cerebral Anterior communicating Middle cerebral Opthalmic Internal carotid
Circle of Willis Posterior communicating Posterior cerebral
Major inputs from aortic arch
Superior cerebellar Pontine Basilar Anterior inferior cerebellar Posterior inferior cerebellar
Vertebral
Major branches of input arteries
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
8
PLATE 2A GW7 Coronal CR 17.5 mm M2155 Level 2: Section 116 Peripheral neural and non-neural structures labeled Superior sagittal sinus (in interhemispheric fissure) Dural vascular network Branches of anterior cerebral artery in pial vascular network
Superarachnoid reticulum (cell sparse)
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Future skin and skull (cell dense) Future dura (cell dense internal border of skull)
Branches of middle cerebral artery
Pia
Superarachnoid reticulum (cell sparse) Hypothetical olfactory induction field
Nerve I (olfactory) Olfactory epithelium Eyelid
Nasal cavity Nasal epithelium
Zygomatic bone?
Maxilla
Oral cavity
Nasal septum
Mandible
Level 2: Computer-aided 3-D Brain Reconstruction
PLATE 2B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Central neural structures labeled Interhemispheric fissure
TELENCEPHALON
Dural outline is external border of superarachnoid reticulum
CEREBRAL CORTEX
Neocortical NEP
Brain surface (heavier line)
Cingulate dorsal pool
telencephalic superventricle
(future lateral ventricle)
Cortical primordial plexiform layer
Limbic cortical NEP
Migrating Cajal-Retzius cells and subplate neurons
Hippocampal
Limbic cortical (insular) NEP
Corticoganglionic NEP
Fornical GEP
Migrating neurons originating in corticoganglionic NEP
Choroid plexus stem cells
Migrating basal ganglionic neurons
Anterolateral ganglionic NEP
ventral pool
Basal telencephalic NEP BASAL GANGLIA/ BASAL TELENCEPHALON
Septal NEP
Settling basal ganglionic neurons
Migrating basal telencephalic neurons Settling basal telencephalic neurons
Migrating and settling septal neurons
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
9
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PLATE 3A GW7 Coronal CR 17.5 mm M2155 Level 3: Section 164
Peripheral neural and non-neural structures labeled Superior sagittal sinus (in interhemispheric fissure) Dural vascular network
Branches of anterior cerebral artery in pial vascular network The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Anterior cerebral artery Superarachnoid reticulum (cell sparse)
Future skin and skull (cell dense)
Vascular bed of choroid plexus
Future dura (cell dense internal border of skull) Pia
Branches of middle cerebral artery Orbito-sphenoid process
Superarachnoid reticulum (cell sparse)
Hypothetical olfactory induction field
Nerve I (olfactory)
Eye
Eyelid Earliest ganglion cells Sclera Intraretinal space Cornea Lens Vitreous body Retinal NEP Pigment epithelium
Olfactory epithelium
Nasal cavity Nasal epithelium Nasal septum
Tongue
Zygomatic bone? Maxilla
Palatal process Oral cavity Mandible
Level 3: Computer-aided 3-D Brain Reconstruction
Lingual epithelium
11
PLATE 3B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Central neural structures labeled Interhemispheric fissure
TELENCEPHALON
Dural outline is external border of superarachnoid reticulum
CEREBRAL CORTEX
Neocortical NEP Cingulate Hippocampal
telencephalic superventricle
(future lateral ventricle)
Brain surface (heavier line)
dorsal pool
Fornical GEP Telencephalic
Limbic cortical (insular) NEP
Choroid plexus stem cells Diencephalic
Corticoganglionic NEP
third ventricle foramen of monro
Anterolateral ganglionic NEP
ventral pool
Anteromedial ganglionic NEP BASAL GANGLIA/ BASAL TELENCEPHALON
Cortical primordial plexiform layer
Limbic cortical NEP
Basal telencephalic NEP Septal NEP
Migrating Cajal-Retzius cells and subplate neurons Migrating neurons originating in corticoganglionic NEP? Migrating basal ganglionic neurons Pioneer internal capsule axons Settling basal ganglionic neurons Migrating basal telencephalic neurons
Settling basal telencephalic neurons Migrating and settling septal neurons
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
12
PLATE 4A GW7 Coronal CR 17.5 mm M2155 Level 4: Section 201
See a high magnification view of the thalamus and cerebral cortex in Plates 18A and B. Peripheral neural and non-neural structures labeled Superior sagittal sinus
Superarachnoid reticulum (cell sparse)
Dural vascular network Anterior cerebral artery
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Future skin and skull (cell dense) Future dura (cell dense internal border of skull)
Vascular bed of choroid plexus
Future parietal bone?
Pia
Branches of middle cerebral artery in pial vascular network Superarachnoid reticulum (cell sparse) Orbito-sphenoid process
Eye
Nerve II (optic) Eyelid Sclera Intraretinal space Vitreous body Retinal NEP Ganglion cells Pigment epithelium
Lingual epithelium
Ethmoid bone? Tongue
Maxilla
Palatal process Oral cavity
Meckel's cartilage
Level 4: Computer-aided 3-D Brain Reconstruction
PLATE 4B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Neocortical NEP
Cingulate Hippocampal
Limbic cortical NEP
telencephalic superventricle
Corticoganglionic NEP
posterior pool Choroid plexus stem cells
for of mamen onr o
Posterior ganglionic NEP Basal telencephalic NEP
(PREOPTIC AREA)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Cortical primordial plexiform layer
Migrating Cajal-Retzius cells and subplate neurons Migrating neurons originating in corticoganglionic NEP? Pioneer internal capsule axons Migrating basal ganglionic neurons Settling basal ganglionic (globus pallidus?) neurons Settling basal telencephalic neurons Migrating basal telencephalic neurons Settling basal telencephalic neurons
preoptic preoptic pool pool
BASAL GANGLIA/ BASAL TELENCEPHALON
DIENCEPHALON
Brain surface (heavier line)
Fornical GEP
(future lateral ventricle) Limbic cortical (insular) NEP
Dural outline is external border of superarachnoid reticulum
thalamic thalamic pool pool
CEREBRAL CORTEX
(future third ventricle)
(THALAMUS)
TELENCEPHALON
Dorsal thalamic NEP Migrating thalamic Reticular NEP neurons Anterior thalamic NEP
diencephalic superventricle
DIENCEPHALON
Central neural structures labeled
Preoptic NEP Migrating preoptic neurons
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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PLATE 5A GW7 Coronal CR 17.5 mm M2155 Level 5: Section 242
See a high magnification view of the thalamus and cerebral cortex from Section 236 in Plates 19A and B. Peripheral neural and non-neural structures labeled Superior sagittal sinus
Superarachnoid reticulum (cell sparse)
Dural vascular network
Anterior cerebral artery The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Branches of anterior cerebral artery Future skin and skull (cell dense) Future dura (cell dense internal border of skull)
Vascular bed of choroid plexus
Pia
Future parietal bone? Branches of middle cerebral artery in pial vascular network Superarachnoid reticulum (cell sparse)
Orbito-sphenoid process Nerve II (optic)? Future ethmoid/ sphenoid bones Lingual epithelium
Maxilla Palatal process
Meckel's cartilage
Tongue
Salivary gland?
Level 5: Computer-aided 3-D Brain Reconstruction
Oral cavity
PLATE 5B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Central neural structures labeled
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
(EPITHALAMUS AND THALAMUS)
Migrating thalamic neurons
Dorsal
Thalamic NEP
Ventral
TELENCEPHALON
Dural outline is external border of superarachnoid reticulum
Reticular
CEREBRAL CORTEX Limbic cortical NEP
Migrating epithalamic neurons
Epithalamic NEP
DIENCEPHALON
Anterior
Retrosplenial? Hippocampal
thalamic pool
Cortical primordial plexiform layer
telencephalic superventricle
diencephalic superventricle
Fornical GEP
(future lateral ventricle)
posterior pool
Limbic cortical (insular) NEP
Choroid plexus stem cells
Corticoganglionic NEP
(future third ventricle)
Neocortical NEP
foramen of monro
Posterior ganglionic NEP Strionuclear NEP
Preoptic NEP
(HYPOTHALAMUS)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Pioneer internal capsule axons
Settling basal telencephalic neurons
Lateral preoptic pool
Medial
optic recess
Optic nerve GEP Chiasmatic GEP
DIENCEPHALON
Migrating neurons originating in corticoganglionic NEP?
Migrating bed nucleus of the stria terminalis neurons
BASAL GANGLIA/ BASAL TELENCEPHALON
(PREOPTIC AREA)
Migrating Cajal-Retzius cells and subplate neurons
Migrating basal ganglionic neurons
Basal telencephalic NEP
DIENCEPHALON
Brain surface (heavier line)
(intermingled with anterobasal hypothalamic NEP?)
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Migrating basal telencephalic neurons Medial forebrain bundle? Migrating lateral preoptic neurons Anterobasal nuclear neurons?
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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PLATE 6A GW7 Coronal CR 17.5 mm M2155 Level 6: Section 283
Peripheral neural and non-neural structures labeled Superior sagittal sinus
Superarachnoid reticulum (cell sparse)
Dural vascular network
Branches of anterior cerebral artery in pial vascular network Future skin and skull (cell dense)
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Future dura (cell dense internal border of skull)
Pia Future parietal bone Middle cerebral artery Circle of Willis artery
Superarachnoid reticulum (cell sparse)
Carotid artery
Car otid arte ry
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Trigeminal ganglion (V) Ali-sphenoid process? Pituitary gland (anterior lobe, adenohypophysis) Palatal process Lingual epithelium
Sphenoid bone (sella turcica) Maxilla Future temporomandibular joint Meckel's cartilage
Tongue Laryngo-tracheal groove Larynx Oral cavity
External auditory meatus (in petrous temporal bone) Petrous temporal bone Salivary gland?
Level 6: Computer-aided 3-D Brain Reconstruction
PLATE 6B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Central neural structures labeled
DIENCEPHALON (EPITHALAMUS, THALAMUS, AND SUBTHALAMUS)
NEP - Neuroepithelium
Migrating epithalamic neurons Epithalamic NEP
Thalamic NEP
Migrating thalamic neurons Dural outline is external border of superarachnoid reticulum
Dorsal Ventral thalamic pool
Reticular
Subthalamic NEP TELENCEPHALON
Cortical primordial plexiform layer
diencephalic superventricle
(future third ventricle)
CEREBRAL CORTEX
Brain surface (heavier line)
Limbic cortical
(retrosplenial?) NEP
Neocortical NEP posterior pool
telencephalic superventricle
Migrating CajalRetzius cells and subplate neurons
(future lateral ventricle)
Amygdaloid NEP
subthalamic pool
Strionuclear NEP? BASAL GANGLIA (AMYGDALA)
hypothalamic pool
Lateral
Hypothalamic NEP
infundibular recess
Anterior
Migrating bed nucleus of the stria terminalis neurons? Migrating subthalamic neurons (zona incerta, Forel's fields) Migrating lateral hypothalamic neurons Migrating anterior hypothalamic neurons
DIENCEPHALON (HYPOTHALAMUS)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Migrating amygdaloid neurons
Medial forebrain bundle?
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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18
PLATE 7A GW7 Coronal CR 17.5 mm M2155 Level 7: Section 325 Superarachnoid
Peripheral neural and non-neural structures labeled Pineal gland
Superior sagittal sinus Dural vascular network
reticulum (cell sparse)
Pial vascular network
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Future skin and skull (cell dense) Future dura (cell dense internal border of skull) Pia
Future parietal bone
Superarachnoid reticulum (cell sparse)
Middle cerebral artery and branches Circle of Willis artery Carotid artery
Future squamous temporal bone?
Ali-sphenoid process Pituitary gland
Trigeminal ganglion (V)
Anterior lobe, adenohypophysis
Nerve V (trigeminal) Sphenoid bone (sella turcica)
Posterior lobe, neurohypophysis
Facial ganglion (VII)?
Temporal bone labyrinth
External auditory meatus
Inferior glossopharyngeal ganglion (IX)?
Petrous temporal bone
Esophagus
Level 7: Computer-aided 3-D Reconstruction
19
PLATE 7B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Pineal GEP
DIENCEPHALON
Migrating epithalamic neurons
Epithalamic NEP
(EPITHALAMUS, AND THALAMUS)
Posterior (dorsal lateral geniculate)
Thalamic NEP
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Central neural structures labeled
Dural outline is external border of superarachnoid reticulum
Ventral
thalamic pool
Reticular
Migrating thalamic neurons
diencephalic superventricle
(future third ventricle)
Dorsal lateral geniculate
TELENCEPHALON CEREBRAL CORTEX Cortical primordial plexiform layer
Migrating CajalRetzius cells and subplate neurons Neocortical NEP
Ventrobasal complex Reticular nucleus Brain surface (heavier line)
Migrating subthalamic neurons (zona incerta, Forel's fields) Migrating lateral hypothalamic neurons
subthalamic pool
hypothalamic pool
Subthalamic NEP Lateral
Medial forebrain bundle?
Hypothalamic NEP DIENCEPHALON
(SUBTHALAMUS AND HYPOTHALAMUS)
Dorsomedial/ventromedial complex? Arcuate nucleus?
Middle
Migrating middle hypothalamic neurons
infundibular recess
Median eminence/ neurohypophysis (pituicyte) GEP
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
20
PLATE 8A Peripheral neural and non-neural structures labeled
GW7 Coronal CR 17.5 mm M2155 Level 8: Section 375 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Superior sagittal sinus Dural vascular network
Superarachnoid reticulum (cell sparse)
Pial vascular network
Future skin and skull (cell dense) Future dura (cell dense internal border of skull)
Future parietal bone
Pia
Superarachnoid reticulum (cell sparse)
Middle cerebral artery and branches
Circle of Willis arteries? Basilar artery Trigeminal
Nerve V (trigeminal)
* boundary cap (V)
Posterior cerebral artery
Vestibulocochlear * boundary cap (VIII)
Future squamous temporal bone? Nerve VIII (vestibulocochlear)
Facial
Temporal bone labyrinth (otic vesicle)
* boundary
cap (VII)?
Vestibular ganglion (VIII)
Petrous temporal bone
Vertebral artery? Spiral ganglion (VIII)?
Immature cochlea and semicircular canals
Superarachnoid reticulum (cell sparse) Basal occipital bone Basilar artery
Level 8: Computer-aided 3-D Brain Reconstruction
* Boundary caps are
Schwann cell GEPs?
PLATE 8B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
MESENCEPHALON
Posterior commissural GEP
(PRETECTUM)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Central neural structures labeled
Posterior commissure Migrating pretectal neurons
Pretectal NEP mesencephalic superventricle
Brain surface (heavier line)
(future aqueduct)
Dural outline is external border of superarachnoid reticulum
DIENCEPHALON Posterior (dorsal lateral geniculate) thalamic pool Posterior (medial geniculate)
Dorsal lateral geniculate
diencephalic superventricle
(future third ventricle)
Thalamic NEP
Migrating thalamic neurons
Reticular
Medial geniculate
Reticular nucleus Migrating subthalamic neurons (zona incerta, Forel's fields) Settling subthalamic nuclear neurons?
subthalamic pool
Subthalamic NEP
hypothalamic pool
Medial forebrain bundle?
Hypothalamic NEP
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)
(middle) Medial lemniscus?
RHOMBENCEPHALON
Central trigeminal tract?
(PONS)
Longitudinal domains of migrating and settling pontine neurons
Principal sensory nucleus (V)? Caudal extension of trigeminal nuclear complex (V)? Lateral lemniscus?
Lateral Intermediate Medial
Pontine reticular formation Migrating raphe nuclear complex neurons Midline raphe glial structure
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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22
PLATE 9A GW7 Coronal CR 17.5 mm M2155 Level 9: Section 410
See a high magnification view of the mesencephalon and diencephalon Peripheral neural and from Section 390 in non-neural structures labeled Plates 20A and B. Superior sagittal sinus
Dural vascular network
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Pial vascular network
Future skin and skull (cell dense)
Superarachnoid reticulum (cell sparse)
Future dura (cell dense internal border of skull) Pia
Future parietal bone Middle cerebral artery
Superarachnoid reticulum (cell sparse) Circle of Willis arteries? Basilar artery Trigeminal
Posterior cerebral artery and branches
* boundary cap (V)?
Future squamous temporal bone Vestibulocochlear * boundary cap (VIII)
Petrous temporal bone
Temporal bone labyrinth (immature cochlea and semicircular canals) Mastoid air cells? Nerve and ganglion IX (glossopharyngeal) Basal occipital bone
Foramen magnum Basilar artery
Superarachnoid reticulum (cell sparse)
* Boundary caps are
Level 9: Computer-aided 3-D Brain Reconstruction
Schwann cell GEPs?
PLATE 9B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
MESENCEPHALON (PRETECTUM)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Central neural structures labeled Posterior commissure
Posterior commissural GEP
Migrating pretectal neurons Brain surface (heavier line)
Pretectal NEP
Dural outline is external border of superarachnoid reticulum
mesencephalic superventricle
(future aqueduct)
DIENCEPHALON
Migrating thalamic neurons
Posterior (medial geniculate)
Medial geniculate? thalamic pool
Thalamic NEP
Reticular nucleus
Reticular
diencephalic superventricle
(future third ventricle)
Migrating subthalamic neurons (Forel's fields and zona incerta?) Medial forebrain bundle?
Subthalamic NEP subthalamic pool
hypothalamic pool
Hypothalamic NEP
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)
(middle)
PONS
Midline raphe glial structure Midline raphe glial structure GEP Medial pontine NEP Lateral pontine NEP
CEREBELLUM
Cerebellar NEP
Auditory (cochlear) NEP
Nerve VII (genu)
Medial longitudinal fasciculus
Lateral medullary NEP
Medial lemniscus? Migrating raphe nuclear complex neurons Central trigeminal tract? Migrating trigeminal nuclear complex neurons?
Pontine reticular formation
Migrating cerebellar deep nuclear neurons?
Facial motor neurons
Premigratory Migrating
Sojourning Purkinje cells?
Settling?
Migrating cochlear nuclear neurons?
Medial medullary NEP
Ventral nucleus of the lateral lemniscus?
Midline raphe glial structure GEP
UPPER MEDULLA
Lateral lemniscus? Superior olivary complex
RHOMBENCEPHALON
Medullary reticular formation Migrating raphe nuclear complex neurons? Midline raphe glial structure
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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24
PLATE 10A GW7 Coronal CR 17.5 mm M2155 Level 10: Section 424 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Peripheral neural and non-neural structures labeled Superior sagittal sinus
Superarachnoid reticulum (cell sparse)
Dural vascular network
Future skin and skull (cell dense) Pial vascular network Future dura (cell dense internal border of skull)
Future parietal bone
Pia Superarachnoid reticulum (cell sparse)
Middle cerebral artery
Circle of Willis arteries? Basilar artery
Posterior cerebral artery and branches
Future squamous temporal bone Vestibulocochlear boundary cap * (VIII)?
* Boundary caps are
Schwann cell GEPs?
Temporal bone labyrinth Petrous temporal bone Nerve and ganglion IX (glossopharyngeal)? Nerve and ganglion X (vagus)? Basilar artery
Foramen magnum
Mastoid air cell? Basal occipital bone Superarachnoid reticulum (cell sparse)
Level 10: Computer-aided 3-D Brain Reconstruction
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
MESENCEPHALON
PLATE 10B
Central neural structures labeled
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Posterior commissure
Posterior commissural GEP
Brain surface (heavier line)
Pretectal NEP
Migrating pretectal neurons mesencephalic superventricle
Dural outline is external border of superarachnoid reticulum
(future aqueduct)
Migrating central gray neurons? Mesencephalic reticular formation
Mesencephalic tegmental NEP
Migrating red nuclear neurons? Migrating interpeduncular nuclear neurons?
DIENCEPHALON Subthalamic NEP
Migrating subthalamic neurons
subthalamic pool
Medial forebrain bundle?
diencephalic superventricle
(future third ventricle)
Hypothalamic NEP
(mammillary)
PONS
Midline raphe glial structure GEP Medial pontine NEP Lateral pontine NEP
Medial longitudinal fasciculus
CEREBELLUM Cerebellar NEP
Migrating mammillary neurons
hypothalamic pool
Lateral lemniscus? Medial lemniscus?
Dorsal nucleus of the lateral lemniscus?
CTF1 (fibers) CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons) CTF6 (cells-Purkinje cells)
Pontine reticular formation
Upper rhombic lip
Nerve VII (genu)
Auditory (cochlear)
NEP Lateral medullary NEP
Abducens nucleus (VI)? Medial longitudinal fasciculus
rhombencephalic superventricle
(future fourth ventricle)
Premigratory facial motor nucleus (VII) neurons?
Lower rhombic lip Migrating vestibular nuclear complex neurons?
Medial medullary NEP
UPPER MEDULLA
Layers of the cerebellar transitional field
Vestibular nuclear complex?
Midline raphe glial structure GEP
Migrating cochlear nuclear neurons? Spinal nucleus and tract (V)? Settling facial motor nucleus (VII) neurons?
RHOMBENCEPHALON
Superior olivary complex Medullary reticular formation Migrating raphe nuclear complex neurons? Midline raphe glial structure
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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26
PLATE 11A GW7 Coronal CR 17.5 mm M2155 Level 11: Section 444 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Peripheral neural and non-neural structures labeled Superior sagittal sinus
Superarachnoid reticulum (cell sparse)
Dural vascular network
Future skin and skull (cell dense) Pial vascular network Future dura (cell dense internal border of skull) Pia
Future parietal bone Middle cerebral artery
Circle of Willis arteries?
Superarachnoid reticulum (cell sparse)
Basilar artery
Posterior cerebral artery and branches
Future squamous temporal bone
Temporal bone labyrinth
Petrous temporal bone
Foramen magnum Basal occipital bone
Superarachnoid reticulum (cell sparse) Basilar artery
Vagal ganglion (X)? Mastoid air cells?
Level 11: Computer-aided 3-D Brain Reconstruction
PLATE 11B
Central neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Posterior commissure
MESENCEPHALON
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Brain surface (heavier line)
Posterior commissural GEP
Migrating pretectal neurons
Pretectal NEP
Dural outline is external border of superarachnoid reticulum
mesencephalic superventricle
(future aqueduct)
Migrating central gray neurons? Mesencephalic reticular formation
Mesencephalic tegmental NEP
Migrating red nuclear neurons? Migrating oculomotor (III) nuclear neurons Medial forebrain bundle?
DIENCEPHALON diencephalic superventricle
Migrating mammillary neurons
(future third ventricle, mammillary recess)
Hypothalamic NEP (mammillary) PONS
Midline raphe glial structure Midline raphe glial structure GEP Medial longitudinal fasciculus Medial pontine NEP Lateral pontine NEP
Lateral lemniscus? Medial lemniscus?
rhombencephalic superventricle
(future fourth ventricle)
Layers of the cerebellar transitional field CTF1 (fibers) CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons)? CTF6 (cells-Purkinje cells)
Pontine reticular formation
CEREBELLUM Cerebellar NEP
Medial cerebellar notch
Upper rhombic lip Medullary velum
Precerebellar NEP Lateral medullary NEP
Abducens nucleus (VI)? Medial longitudinal fasciculus
Lower rhombic lip Medullary reticular formation
Posterior intramural migratory stream (inferior olivary neurons)?
Medial medullary NEP
MEDULLA
Solitary nucleus and tract?
Midline raphe glial structure GEP
Vestibular nuclei? Settling facial motor nuclear (VII) neurons
RHOMBENCEPHALON
Inferior olive? Migrating raphe nuclear complex neurons? Midline raphe glial structure
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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28
PLATE 12A GW7 Coronal CR 17.5 mm M2155 Level 12: Section 500
Peripheral neural and non-neural structures labeled Superior sagittal sinus
The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Dural vascular network
Pial vascular network Pia
Superarachnoid reticulum (cell sparse)
Future skin and skull (cell dense) Nerve III (oculomotor)
Posterior cerebral artery
Future dura (cell dense internal border of skull)
Future squamous temporal bone
Temporal bone labyrinth
Glossopharyngeal
* boundary cap (IX)? Vagal boundary * cap (X)? Vertebral artery?
Future squamous occipital bone Superarachnoid reticulum (cell sparse)
Traces of the vagal (X) and glossopharyngeal (IX) nerve sheaths?
* Boundary caps are
Schwann cell GEPs?
Level 12: Computer-aided 3-D Brain Reconstruction
29 FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 12B
Central neural structures labeled
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Posterior commissure
MESENCEPHALON
Migrating neurons and glia invade posterior commissure
Posterior commissural GEP
Pretectal NEP
Migrating pretectal neurons mesencephalic superventricle
Brain surface (heavier line)
(future aqueduct)
Migrating central gray neurons?
Mesencephalic tegmental NEP
Mesencephalic reticular formation Migrating red nuclear neurons? Migrating oculomotor (III) nuclear neurons Medial forebrain bundle? Migrating and settling substantia nigra neurons? Migrating and settling ventral tegmental area neurons?
PONS
Dural outline is external border of superarachnoid reticulum
Midline raphe glial structure Midline raphe glial structure GEP
Medial lemniscus?
Medial longitudinal fasciculus
Lateral lemniscus?
Medial pontine NEP
Layers of the cerebellar transitional field CTF1 (fibers)
Pontine reticular formation
Lateral pontine NEP
CTF2 (cells-deep neurons) CTF3 (fibers)
CEREBELLUM
CTF4-5 (cells-deep neurons)? CTF6 (cells-Purkinje cells)
Cerebellar NEP
Upper rhombic lip
metencephalic pool
Lateral
Medial
rhombencephalic superventricle (future fourth ventricle)
Cerebellar notches
MEDULLA
Precerebellar NEP
myelencephalic pool
Medial longitudinal fasciculus
Vestibular nuclei?
Medullary reticular formation
Medullary velum
Lower rhombic lip
Lateral medullary NEP Migrating precerebellar nuclear neurons
Medial medullary NEP
Solitary nucleus and tract
Midline raphe glial system GEP
Posterior intramural migratory stream (inferior olivary neurons)?
RHOMBENCEPHALON
Migrating raphe nuclear complex neurons? Midline raphe glial structure Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
30
PLATE 13A GW7 Coronal CR 17.5 mm M2155 Level 13: Section 533 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Superior sagittal sinus
Peripheral neural and non-neural structures labeled
Pia
Pial vascular network
Dural vascular network
Interpeduncular fossa
Superarachnoid reticulum (cell sparse)
Future skin and skull (cell dense)
Future dura (cell dense internal border of skull)
Future squamous temporal bone?
Level 13: Computer-aided 3-D Brain Reconstruction
Vagal boundary * cap (X)? Superarachnoid reticulum (cell sparse)
* Boundary caps are
Schwann cell GEPs?
Traces of the vagal (X) nerve sheath?
Future squamous occipital bone?
Traces of the hypoglossal (XII) nerve sheath?
PLATE 13B
Central neural structures labeled
Posterior commissural GEP Posterior commissure Migrating glia invade posterior commissure
MESENCEPHALON TECTUM
Migrating pretectal neurons
Pretectal NEP
mesencephalic superventricle
Brain surface (heavier line)
(future aqueduct)
TEGMENTUM
Migrating central gray neurons? Mesencephalic reticular formation
Mesencephalic tegmental NEP
Migrating oculomotor (III) nuclear neurons Settling red nuclear neurons? Medial forebrain bundle? Migrating and settling substantia nigra neurons?
ISTHMUS
Migrating and settling ventral tegmental area neurons? Midline raphe glial structure
Midline raphe glial structure GEP
Medial longitudinal fasciculus
isthmal canal
Lateral lemniscus? Layers of the cerebellar transitional field
Isthmal NEP
CTF1 (fibers)
Mesencephalic reticular formation
CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons)?
CEREBELLUM
CTF6 (cells-Purkinje cells)
Cerebellar NEP Upper rhombic lip
metencephalic pool
Medial
rhombencephalic superventricle
Lateral
(future fourth ventricle)
Cerebellar notches
myelencephalic pool
Dural outline is external border of superarachnoid reticulum
Vestibular nuclei
MEDULLA
Medullary velum
Precerebellar NEP Lateral medullary NEP
Medial longitudinal fasciculus Midline raphe glial structure GEP
SPINAL CORD
Migrating precerebellar nuclear neurons Solitary nucleus and tract
Medial medullary NEP
RHOMBENCEPHALON
Lower rhombic lip
Medullary reticular formation
Floor plate Ventral spinal G/EP
Posterior intramural migratory stream (inferior olivary neurons)? Migrating raphe nuclear complex neurons? Midline raphe glial structure Ventral commissure Ventral funiculus Ventral gray Segregating ventral horn motoneuron columns
Ventral horn interneurons
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: CTF - Cerebellar transitional field G/EP - Glioepithelium/ependyma GEP - Glioepithelium NEP - Neuroepithelium
Lateral funiculus Intermediate spinal NEP Dorsal spinal NEP Roof plate
Intermediate gray central canal Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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PLATE 14A GW7 Coronal CR 17.5 mm M2155 Level 14: Section 572 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Superarachnoid reticulum (cell sparse)
Superior sagittal sinus
Peripheral neural and non-neural structures labeled Future skin and skull (cell dense)
Future dura (cell dense internal border of skull) Pia
Pial vascular network
Dural vascular network
Level 14: Computer-aided 3-D Brain Reconstruction Future squamous occipital bone?
Superarachnoid reticulum (cell sparse, fluid-filled spaces)
PLATE 14B
Central neural structures labeled
Posterior commissural GEP Posterior commissure Migrating glia invade posterior commissure
MESENCEPHALON TECTUM
Migrating superior collicular neurons Tectal (superior collicular) NEP Brain surface (heavier line)
mesencephalic superventricle (future aqueduct)
Dural outline is external border of superarachnoid reticulum
Tectal (inferior collicular) NEP Migrating inferior collicular neurons
TEGMENTUM
Migrating central gray neurons?
Mesencephalic tegmental NEP
Migrating trochlear (IV) nuclear neurons Lateral lemniscus? Mesencephalic reticular formation
ISTHMUS
isthmal canal
Medial longitudinal fasciculus Migrating isthmal neurons
Isthmal NEP
Layers of the cerebellar transitional field
CEREBELLUM
CTF1 (fibers) CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons)? CTF6 (cells-Purkinje cells)
Cerebellar NEP
Upper rhombic lip Medial
metencephalic pool
Lateral Cerebellar notches
rhombencephalic superventricle
Medullary velum
(future fourth ventricle)
MEDULLA
Vestibular nuclei
Lower rhombic lip
myelencephalic pool
Precerebellar NEP
Migrating precerebellar nuclear neurons
Lateral medullary NEP Medial medullary NEP Midline raphe glial structure GEP Medial longitudinal fasciculus
RHOMBENCEPHALON
Ventral commissure
SPINAL CORD
Floor plate Ventral spinal G/EP
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: CTF - Cerebellar transitional field G/EP - Glioepithelium/ependyma GEP - Glioepithelium NEP - Neuroepithelium
Intermediate spinal NEP Dorsal spinal NEP Roof plate
Medullary reticular formation
Solitary nucleus and tract Posterior intramural migratory stream (inferior olivary neurons) Settling inferior olive neurons Migrating raphe nuclear complex neurons? Midline raphe glial structure Ventral funiculus Ventral gray Segregating ventral horn motoneuron columns Ventral horn interneurons
Lateral funiculus Intermediate gray central canal Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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34
PLATE 15A
Superior sagittal sinus
GW7 Coronal CR 17.5 mm M2155 Level 15: Section 588 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Peripheral neural and non-neural structures labeled Future skin and skull (cell dense) Future dura (cell dense internal border of skull)
Pia
Pial vascular network Superarachnoid reticulum (cell sparse)
Level 15: Computer-aided 3-D Brain Reconstruction
Dural vascular network
Future squamous occipital bone?
Superarachnoid reticulum (cell sparse, fluid-filled spaces)
PLATE 15B
Central neural structures labeled MESENCEPHALON Brain surface (heavier line)
TECTUM
Migrating superior collicular neurons
Tectal (superior collicular) NEP
mesencephalic superventricle
Dural outline is external border of superarachnoid reticulum
(future aqueduct)
Tectal (inferior collicular) NEP
Migrating inferior collicular neurons Migrating trochlear (IV) nuclear neurons? isthmal canal
Trochlear nuclear NEP?
ISTHMUS Isthmal NEP
CEREBELLUM
Lateral lemniscus Migrating isthmal neurons Layers of the cerebellar transitional field CTF1 (fibers) CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons)? CTF6 (cells-Purkinje cells)
Cerebellar NEP
Medial cerebellar notch
Upper rhombic lip metencephalic pool Lateral cerebellar notch
rhombencephalic superventricle (future fourth ventricle)
MEDULLA
myelencephalic pool
Medullary velum
Vestibular nuclei
Lower rhombic lip Migrating precerebellar nuclear neurons
Precerebellar NEP
Posterior intramural migratory stream (inferior olivary neurons)?
Lateral medullary NEP Medullary reticular formation
Medial medullary NEP Prepositus, vagal (X), and hypoglossal (XII) nuclei?
Solitary nucleus and tract
Medial longitudinal fasciculus
Migrating raphe nuclear complex neurons?
Midline raphe glial system GEP Midline raphe glial structure
RHOMBENCEPHALON SPINAL CORD FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: CTF - Cerebellar transitional field G/EP - Glioepithelium/ependyma GEP - Glioepithelium NEP - Neuroepithelium
Floor plate Ventral spinal G/EP Intermediate spinal NEP
Settling inferior olive neurons Ventral horn interneurons Lateral funiculus Intermediate gray central canal
Dorsal spinal NEP Roof plate
Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
35
36
PLATE 16A GW7 Coronal CR 17.5 mm M2155 Level 16: Section 628 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Superior sagittal sinus
Peripheral neural and non-neural structures labeled
Future skin and skull (cell dense) Future dura (cell dense internal border of skull) Pia
Pial vascular network Superarachnoid reticulum (cell sparse)
Level 16: Computer-aided 3-D Brain Reconstruction
Dural vascular network
Future squamous occipital bone?
Superarachnoid reticulum (cell sparse, fluid-filled spaces)
PLATE 16B
Central neural structures labeled MESENCEPHALON TECTUM
Brain surface (heavier line)
Migrating superior collicular neurons Tectal (superior collicular) NEP
Dural outline is external border of superarachnoid reticulum
mesencephalic superventricle (future aqueduct)
isthmal canal
Tectal (inferior collicular) NEP
Migrating inferior collicular neurons Lateral lemniscus
Isthmal NEP
ISTHMUS
Vermis
CEREBELLUM
Layers of the cerebellar transitional field CTF1 (fibers)
Intermediate hemisphere Lateral hemisphere
Cerebellar NEP
CTF2 (cells-deep neurons) CTF3 (fibers) CTF4 (cells-deep neurons)
Medial cerebellar notch
CTF5 (fibers) CTF6 (cells-Purkinje cells)
Upper rhombic lip metencephalic pool
Lateral cerebellar notch
Medullary velum
rhombencephalic superventricle (future fourth ventricle)
Rhombencephalic choroid plexus
MEDULLA Choroid plexus stem cells Lower rhombic lip
Vestibular nuclei myelencephalic pool
Precerebellar NEP
Migrating precerebellar nuclear neurons
Lateral medullary NEP
Solitary nucleus and tract lar reticu llary n Meduformatio
Medial medullary NEP
RHOMBENCEPHALON FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Migrating raphe nuclear complex neurons? Cuneate nucleus? Hypoglossal nucleus (XII)?
Dorsal gray Dorsal spinal NEP
Roof plate
SPINAL CORD
Dorsal funiculus central canal
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
37
38 Peripheral neural and non-neural structures labeled
PLATE 17A GW7 Coronal CR 17.5 mm M2155 Level 17: Section 677 The large cell-sparse superarachnoid reticulum defines various brain parenchymal expansion zones. It is sandwiched between external (dural) and internal (pial) vascular networks.
Superior sagittal sinus
Future skin and skull (cell dense) Future dura (cell dense internal border of skull) Pia
Superarachnoid reticulum (cell sparse)
Dural vascular network
Pial vascular network
Level 17: Computer-aided 3-D Brain Reconstruction
Superarachnoid reticulum (cell sparse, fluid-filled spaces)
Future squamous occipital bone?
39 Central neural structures labeled
PLATE 17B
MESENCEPHALON TECTUM
Brain surface (heavier line)
Migrating superior collicular neurons Tectal (superior collicular) NEP
mesencephalic superventricle (future aqueduct)
Dural outline is external border of superarachnoid reticulum
Tectal (inferior collicular) NEP Migrating inferior collicular neurons Lateral lemniscus/ brachium of the inferior colliculus
Layers of the cerebellar transitional field is
CTF1 (fibers)
Ve m
CEREBELLUM
CTF3 (fibers)
EP
CTF4 (cells-deep neurons)
rN
CTF5 (fibers) CTF6 (cells-Purkinje cells)
lla
r he
p mis He e
CTF2 (cells-deep neurons)
C ere
be
metencephalic pool
Upper rhombic lip
Lateral cerebellar notch
rhombencephalic superventricle (future fourth ventricle)
Medullary velum
Rhombencephalic choroid plexus Choroid plexus stem cells
myelencephalic pool
MEDULLA
Medullary velum
Lower rhombic lip
Medullary (gracile?) NEP Migrating gracile nuclear neurons?
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
RHOMBENCEPHALON FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: CTF - Cerebellar transitional field NEP - Neuroepithelium
Medullary velum
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
40
PLATE 18A GW7 Coronal, CR 17.5 mm, M2155 Near Level 4: Section 203
See Level 4 in Plates 4A and B.
CEREBRAL CORTEX AND THALAMUS
PLATE 18B
RAL B RE E C
Cortical primordial plexiform layer
CORT EX
Brain surface (pia, heavier line)
Superarachnoid reticulum
Limbic cortical (cingulate) NEP
Choroid plexus stem cells
Vascular bed of choroid plexus
An
NEP thal ami c
Dor sal
H A L A M
T m ic NE P t Reticu hala mic lar NEP ?
Fornical glioepithelium
s neuron lamic g t ha
(future lateral ventricle posterior pool)
thalamic pool
r a ti n
telencephalic superventricle
t m ig
Limbic cortical (hippocampal) NEP
Scattered pioneer Cajal-Retzius cells and subplate neurons migrate into the primordial plexiform layer.
li e s Ear
U S
Neocortical neuroepithelium (NEP)
diencephalic superventricle
Primordial plexiform layer absent (marks border of fornical glioepithelium)
Thalamic primordial plexiform layer
(future third ventricle)
ala terior th
The superarachnoid reticulum is continuous with the vascular bed of the choroid plexus.
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Primordial plexiform layer absent (marks border of choroid plexus stem cells)
41
42
PLATE 19A GW7 Coronal CR 17.5 mm, M2155 Near Level 5: Section 236
See Level 5 in Plates 5A and B.
CEREBRAL CORTEX AND THALAMUS
PLATE 19B Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. rc r io nte
e
ery a rt l ra reb
Migrating epithalamic neurons
Limbic cortical (insular) NEP foramen of monro
l co
An
Corticoganglionic NEP
T
Migrating and settling anterior thalamic neurons
Migrating Cajal-Retzius cells and subplate neurons Migrating hippocampal neurons
Primordial plexiform layer absent (marks border of fornical glioepithelium) The superarachnoid reticulum is continuous with the vascular bed of the choroid plexus.
Thalamic primordial plexiform layer
Primordial plexiform layer absent (marks border of choroid plexus stem cells) Migrating neurons originating in corticoganglionic NEP?
te ri o
r
Choroid plexus stem cells
(future third ventricle)
T
(future lateral ventricle posterior pool)
diencephalic superventricle
H
Fornical glioepithelium
telencephalic superventricle
A L A M U S helium h o e p iVtem (NE c o a l a m i c n e u r lex tral comp P mple lex Do Reticular c o mp x rsa )
i ep
o
Limbic cortical (hippocampal) NEP
ne
ur
(retrosplenial?) NEP
thalamic pool
ettling thalamic neuro ns and s
e
Brain surface (pia, heavier line)
ting
th
u m Limbic cortical
Cortical primordial plexiform layer
gra
(N
li
Superarachnoid reticulum (cell sparse)
Mi
CEREBRAL CORTEX
) EP
Future dura (internal border of skull)
Epithalamic NEP?
mp lex
A
Neocortical
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Future skin and skull (cell dense)
foramen of monro Posterior ganglionic NEP
Strionuclear NEP
BASAL GANGLIA
Migrating bed nucleus of the stria terminalis neurons
Migrating basal ganglionic neurons
Pioneer internal capsule axons
43
44
PLATE ?A 20A GW7 Coronal CR 17.5 mm M2155 Near Level 9: Section 390
See Level 9 in Plates 9A and B.
DIENCEPHALON AND MESENCEPHALON
45 Posterior commissure
Posterior commissural glioepithelium
Pretectal neuroepithelium (NEP)
Migrating pretectal neurons
PRETECTUM
Brain surface (pia, heavier line)
mesencephalic superventricle
Thalamic NEP
(future aqueduct)
Migrating thalamic neurons
e) (do Pos te rsa l la rior N t e ra E l ge P nic ula t
Clumps of pioneer thalamic axons
Dorsal lateral geniculate?
thalamic pool
(future third ventricle)
lar P icu R e t ar N E le nu c
(
SUBTHALAMUS
diencephalic superventricle
Medial geniculate?
ior NEP ster Po l geniculate) ia ed m
THALAMUS
PLATE 20B
Reticular nucleus
Settling zona incerta neurons? Migrating subthalamic neurons (zona incerta?)
subthalamic pool
Subthalamic NEP SUBTHALAMUS
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Medial forebrain bundle? Migrating and settling lateral hypothalamic neurons?
HYPOTHALAMUS
Middle/posterior hypothalamic NEP Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
Settling subthalamic nuclear neurons?
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP) hypothalamic pool
Superarachnoid reticulum (cell sparse)
46
PART PARTIII: III: GW7 GW7 SAGITTAL SAGITTAL Carnegie Collection specimen #1390 (designated here as C1390) was collected in 1916 from a tubal pregnancy. The crown-rump length (CR) is 18 mm estimated to be at gestational week (GW) 7. C1390 was fixed in formalin, embedded in paraffin, and was cut in 20-µm sagittal sections that were stained with aluminum cochineal. Various orientations of the computer-aided 3-D reconstruction of M2155’s brain is used to show the gross external features of a GW7 brain (Figure 2). Like most sagittally cut specimens, C1390’s sections are not parallel to the midline; Figure 2 shows the approximate rotations in top (B) and back views (C). We photographed 62 sections at low magnification from the left to right sides of the brain. Seven of the sections, mainly from the left side of the brain, are illustrated in Plates 21AB to 27AB. Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) indicate the approximate location of the midline and identify non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (low-contrast images) identify central neural structures. Plates 28AB show three highmagnification sections in the region of the facial nerve genu. The brain of C1390 is at a similar stage of development as M2155, the previous GW7 specimen. Throughout the telencephalon, the neuroepithelium is the most prominent structure surrounding the enlarging telencephalic superventricle. All parts of the neuroepithelium are in “stockbuilding” stage, increasing the shorelines of the expanding telencephalic superventricles as more neuronal stem cells are added. Very few pioneer Cajal-Retzius neurons have migrated into the primordial plexiform layer adjacent to the cortical neuroepithelium. In contrast, the basal ganglionic and basal telencephalic neuroepithelia are adjacent to migrating neurons that form distinctive mounds in the floor of the telencephalon. The sagittal plane is ideal to show the slight evagination of the olfactory neuroepithelium in exactly the same region that is contacted by olfactory nerve fibers. The diencephalic neuroepithelium surrounds a large superventricle. It is shrinking in the hypothalamic and subthalamic areas where stem cells are depleted as they generate neurons. Many migrating and settling young neurons are in the parenchyma surrounding these neuroepithelia. In contrast, the superventricular shoreline is expanding in tha-
lamic areas as the thalamic neuroepithelium continues to add more neuronal precursors than to unload postmitotic neurons. The few neurons outside the thalamic neuroepithelium are best seen in sections grazing the dorsolateral part of the diencephalon. The roof (tectum and pretectum) of the mesencephalon contains a stockbuilding neuroepithelium adjacent to a very thin layer of pioneer migrating neurons. However, bundles of fibers in the posterior commissure are very distinct, and spike-like arrays of cells extend between these bundles. Possibly premigratory neurons produce axons while they are sequestered in the pretectal neuroepithelium. The tegmental and isthmal neuroepithelia are much thinner because most of their neuronal progeny has migrated out. These cells accumulate as inner dense clumps and outer sparse arrays interspersed among the thick subpial fiber band in the tegmental and isthmal parenchyma. Both the pons and medulla have neuroepithelia that are shrinking as stem cells unload their neuronal and glial progeny into an expanding parenchyma. The longitudinal arrays at the pontine flexure are easy to see in the sagittal plane. The genu of the facial motor nerve forms fascicles adjacent to the neuroepithelium in medial sections; these fascicles are adjacent to the pial surface in lateral sections. What is presumed to be the solitary tract is the most prominent internal fiber tract in the medulla. Both the pons and medulla have a thick subpial fibrous layer. Lateral sections show large peripheral sensory nerves contacting the brain. No doubt, many of the superficial fibers are the afferent axons of these ganglia along with ascending fiber tracts from the the spinal cord. All of the peripheral nerves (most clearly shown in the trigeminal nerve) have dense glia (Schwann cells), while central fiber tracts are clear. Thus, peripheral gliogenesis precedes the generation of oligodendrocytes in central fiber tracts. The exceptionally thick cerebellar neuroepithelium, in comparison with the thin adjacent pontine neuroepithelium, is most easily seen in lateral sections where it sharply juts into the rhombencephalic superventricle at the medial cerebellar notch. All parts of the cerebellar neuroepithelium are stockbuilding Purkinje stem cells. Most deep nuclear neurons are migrating in the cellular layers of the cerebellar transitional field.
47
EXTERNAL FEATURES OF THE GW7 BRAIN A.
Pineal evagination
Ep
T h a
mus ala ith
Side view l
A perfect sagittal cut through the brain is parallel to the entire midline. Based on Level 1, the sections of C1390's brain rotate an estimated 8.1º from the midine, 4.3º counterclockwise from the anterior horizontal midline (B, top view), and 3.8º clockwise from the posterior vertical midline (C, back view). In the sections illustrated on the following pages, the anterior brain (top and left) is tilted away from the observer, while the posterior brain (bottom and right) is tilted toward the observer.
Pretectum Superior colliculus
a
t
T e
s
o
C e
b
r e
l
e
l
u
m
Upper rhombic lip
BRAINSTEM FLEXURES 1. Medullary
2
n
p
2. Pontine
o
y
Mammillary body
m u s
l
a t In h fu nd ib ul um
e
tel
Optic evagination
H
s
3
a
h a l a m u s
r
C e r e b B
b
Inferior colliculus
u
Olfactory evagination Preoptic area
u
S
4
Isthm
sal B ae p h a l o n nc
m
anglia l g
u
u s
a as
g m e n t
m
c o r t e
l
x
a
P
Invagination of choroid plexus into fourth ventricle
M
e
d
3. Mesencephalic 4. Diencephalic
u
l
Figure 2. A, The lateral view of the left side of a computer-aided 3-D reconstruction of the brain and upper cervical spinal cord in M2155, the preceding GW7 specimen, which has a similar crown-rump length to C1390 (18 mm and 17.5 mm, respectively). External features are identified as in Figure 1B. The heavy numbered lines refer to brainstem flexures (boxed key). B, Top view of the brain in A shows how C1390's sections rotate right (arrow) from the anterior horizontal midline. C, Back view of the brain in A shows how C1390's sections rotate left (arrow) from the posterior vertical midline.
Medullary velum Lower rhombic lip
l a
1
C.
Pineal evagination
Back view
Superior colliculus
Cerebral cortex (occipital pole)
Spinal cord
Inferior colliculus Cerebellum
Isthmus
Vermis
Hemisphere
B.
Top view
s i d e
Medullary velum
-4.3º Horizontal midline 3.8º L e f t Scale bars = 1 mm
s i d e
Left side
Vertical midline
R i g h t
Invagination of choroid plexus into fourth ventricle
Lower medulla
Right side Spinal cord
PLATE 21A
GW7 Sagittal, CR 18 mm, C1390 Level 1: Slide 13, Section 5
Cell-dense future dura
Ce l l
-den
s e fu
tu
ll d sku in an re sk Cell-sparse superarachnoid reticulum
th (f ph al ut a ur li am etc s ic hi u po r p su d e ol bt ve rv ha nt e la ri n mi t c le r cp ) ic oo le l
ce di
en
ve nt ra l
po ol
te
hypothalamic pool mammillary
recesses
infundibular
optic Nostril Nasal cavity
C
Olfactory epithelium
Maxilla
l c a
T
se
Pituitary (anterior lobe)
vi
ty
o
n
Mandible
ar
metencephalic pool
Sella turcica
Medullary velum
g u e
Sphenoid bone
(future fourth ventricle)
Larynx Arytenoid swellings
Epiglottis
Opening to trachea
Invaginating rhombencephalic choroid plexus
Basal occipital bone
myelencephalic pool Pharynx/esophagus
Vertebral body Cell-sparse superarachnoid reticulum
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Medullary velum
Cell-dense future skin and skull Cell-dense future dura
LEFT S IDE
rhombencephalic superventricle
M IDLINE
Ora
sp
isthmal narrows canal
IN
Sphenoid bone
lel
d oi hn ac r ra pe su
um ul tic re
RIGHT SIDE OF BRA
I (olfa rve Ne
Frontonasal process
e icl tr en rv pe t) su educ lic aqu ha ure cep(fut
Future frontal bone
foramen of monro
s en
"Budding" telencephalic choroid plexus
pretectal narrows
me
le nc do (f ep rs ut h al ur a e li po la c ol te s ra up l e ve r nt ve ri n cl t e) ri cl e
Pia
ry) cto
48
49
PLATE 21B TELENCEPHALON
i
m
a
Is
NEP
urons
l ne ma ist h
at
al
l
mic NE P Subt hal a in ial longitu g Med din po al fa sc
in
g
t
lp
r di a
o
a
Preop ti c
NE
P
M
i gr
Migrating cerebellar deep nuclear neurons
Pontine NEP
at Migr
Nerve IV (trochlear)
Upper rhombic lip
ic
Medial lemniscus? (intermingled with midline raphe glial system)
Inferior collicular
m Cerebellar NEP (vermis)
th
( t e c t a
s on ur e n ic lam a th ns po uro hy ne g e n n ati ti n ? igr us M ul
l i c h a e p
Future optic tract?
Anterior
c
EP c N Posterior i m (mammillary) ala th o p Middle Hy
P
Migrating preoptic neurons
Migrating subthalamic neurons
E
Migrating septal neurons
Superior collicular
tal) N
tel M en igr ce at ph ing ali b c n as eu al ro ns
? ea ar
Septal NEP
Basal telencephalic NEP
tral teg me Ven nt al
tal en
Migrating olfactory neurons
Olfactory cortical NEP? Olfactory bulb NEP
n
Reticular
e e
h
T
cephali en es Migrating tegm M
M
Pretectal NEP
s
Dorsal complex
Anterior complex Brain surface (heavier line)
Posterior commissural GEP
men eg ro ns (t neu
N e o c
Epithalamic NEP
c
Primo
Limbic cortical NEP
Migrating pretectal neurons
Posterior complex
c
Hippocampal Fornical GEP
Posterior commissure
E P
N
N E P
lex ifo r r
Cingulate/ retrosplenial
)
i
c
a
P N E
l
MESENCEPHALON
l
m
er lay
DIENCEPHALON Migrating thalamic neurons
Pontomedullary trench
( st
Midline raphe GEP
t
s) tem xure sys fle a l s t em g li a in he r b r rap t fo ne por dli up Mi ural s
ruc
t ing me d
u
eu
ro
ns
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
lus l funicu Ventra Ventral gray
n
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Lower medullary NEP
ry
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Posterior intramural migratory stream (inferior olive neurons?)
lla
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Upper medullary NEP Migra
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Lower rhombic lip
Intermediate gray Dorsal gray Dorsal funiculus
SPINAL CORD
RHOMBENCEPHALON
Labeled on this page: Central neural structures
PLATE 22A llCe
Cell-dense future dura
d
GW7 Sagittal, CR 18 mm, C1390 Level 2: Slide 12, Section 5
skull and kin re s u t e fu Cell-sparse superarachnoid reticulum ens
c li e le) ha icltric p r e t en nc en v le rv eral e t pe lat suure
e
ol po
Future frontal bone Frontonasal process
ph
ut
ce
foramen of monro
ol
recesses
mammillary
Sphenoid bone
optic infundibular
Maxilla
Pituitary (posterior lobe)
metencephalic pool
RAIN
Sella turcica
it
Pituitary (anterior Or lobe) al ca v Sphenoid bone
se ar sp lle C
isthmal narrows canal
m lu cu eti r id no ch ra a er up
LEFT S IDE OF B
hypothalamic pool
M ID L I N E
po
E
l
S ID
ra
T GH RI
nt
e icl tr en rv pe t) su educ lic aqu ha ure cep(fut
ve
s en
"Budding" telencephalic choroid plexus*
pretectal narrows
me
ut (f
(f
al rs do
th al ural am i e c ic th s po ir up d e ol su ve r bt nt v ha ri en la cl t mi cp e) r ic oo l l
Pia
di en
50
y
T g u e o n
Mandible
rhombencephalic superventricle (future fourth ventricle)
Medullary velum
Larynx
Incipient rhombencephalic choroid plexus
Basal occipital bone
Epiglottis Pharynx
Arytenoid swellings myelencephalic pool Laryngotracheal groove
Medullary velum
Cell-sparse superarachnoid reticulum n um col ral ies) b e t d Ver (bo
*At GW7, the telencephalic choroid plexus is beginning to "bud," while the rhombencephalic choroid plexus is marked only by an incipient indentation in the medullary velum. Compare with GW7.5, C6202, Plates 207A and B in Volume 4, pages 514-515.
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-sparse superarachnoid reticulum
Cell-dense future skin and skull Cell-dense future dura
PLATE 22B TELENCEPHALON
DIENCEPHALON
MESENCEPHALON
Migrating thalamic neurons
Cingulate/ retrosplenial Hippocampal
c
Posterior
a
Limbic cortical NEP
Dorsal
h
T
e e
n
Ventral tegmental area?
Septal NEP
ig
l N
Posterior (mammillary)
la
Migrating preoptic neurons
Nerve IV (trochlear)
th
ha ot
Is
H
yp
Middle
Inferior colliculus collicular
P
Anterior
Migrating hypothalamic neurons
E
Preoptic NEP
ic
E
ma
m
ic
N
EP
Interpeduncular nucleus?
N
ra t an ing d ba se sa pt l al te ne len ur ce on ph s al
Superior colliculus collicular
(tectal)
M
l) NE t a urons P e n l ne ta
M e s enc M
m
Basal telencephalic NEP
c ali ph ce
ic (te al g h p ting teg me e ra n g i
Anterior
Olfactory bulb NEP
Migrating olfactory neurons
M
Pretectal NEP
Reticular Cingulate/ prefrontal?
Brain surface (heavier line)
Posterior commissural GEP
Epithalamic NEP
l
a
c
Posterior commissure
P N E
m
i
Fornical GEP
N e o
r di a
i c
N E P
s
Primo
t
a l
P
lp
r
lex ifo r o
m
er lay
Migrating cerebellar deep nuclear neurons
Cerebellar NEP (vermis)
Future optic tract?
Pontine NEP Midline raphe glial system
(structural support for brainstem flexures)
Dorsal Upper rhombic lip
Midline raphe glial structure GEP Pontomedullary trench Midline raphe glial structure GEP
M
Upper medullary NEP
ig ra
ti ng
an d
Vestibular nuclear complex?
se ttl Solitary nuclear complex?
N LO HA BE
NC
EP
s
Labeled on this page: Central neural structures
SPINAL CORD
on
s niculu ral fu Late
s niculu ral fu Vent y al gra Ventr gray te edia Interm Dorsal gray Dorsal funiculus
Lower Ventral rhombic lip
OM
edullary n g m eu r
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Posterior intramural migratory stream (inferior olive neurons?)
RH
in
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Lower medullary NEP
Solitary tract
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
51
52
PLATE 23A
RIGHT
ll- d Ce
en
u tu se f
d in an re sk
skull
SID E
MI
Cell-sparse Cell sparse superarachnoid reticulum
Cell-dense future dura
GW7 Sagittal, CR 18 mm, C1390 Level 3: Slide 11, Section 5 DL INE
LE FT
Pia
SI D
thalamic pool
(future third ventricle)
nc
pretectal narrows
ep (f
a
tu
r
l
ic
e
u
a
Diencephalic/telencephalic choroid plexus
h
u
ed
t)
ntricle
ol po
Nerve III (oculomotor) mammillary
isthmal narrows canal
um ul tic re d i no ch ra ra e p su se ar p s llCe
hypothalamic pool Nasal septum
optic infundibular Sphenoid bone
Or
al
Pituitary (anterior lobe) ca v it
y
Sphenoid bone
Sella turcica
ve
uc
l ra nt ve
foramen of monro
recesses
Maxilla
er
u
(future lateral ventricle)
Frontonasal process
p
q
telencephalic superventricle
Future frontal bone
N
s
al rs o d
mese
diencephalic superventricle
ol po
EO FB RA I
metencephalic pool
T g u e o n
Mandible
rhombencephalic superventricle (future fourth ventricle)
Medullary velum
Incipient rhombencephalic choroid plexus
Pharynx
Arytenoid swellings
Basal occipital bone
Laryngotracheal groove
lic ha ep nc l ele p o o
Epiglottis
my
Larynx
Medullary velum Vertebral column (bodies)
Cell-sparse superarachnoid reticulum Cell-dense future skin and skull
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-dense future dura
PLATE 23B TELENCEPHALON
DIENCEPHALON Migrating thalamic neurons NEP ic m a l
Migrating Cajal-Retzius cells and subplate neurons
r aye EP ml r l N o a if t i c x e te l or la
h
a
Epithalamic NEP
Pretectal NEP
M
n
sen M e Oc c
E
ma
l
N ic la ha ot
yp
Middle
Nerve IV (trochlear)
t
h
H
Migrating preoptic neurons Lamina terminalis Migrating hypothalamic neurons Future optic tract?
N
Preoptic NEP
Inferior collicular
Anterior
Is
s ro n
and s
Pontine NEP
Migrating
Sprouting facial nerve (VII)
Upper rhombic lip
Pontomedullary trench
Migrating facial motor neurons (VII)?
Migrating cerebellar deep nuclear neurons
Cerebellar NEP
et t
g lin
neu tine pon
E
Migrating isthmal neurons
N
m
Posterior (mammillary)
P
EP
Interpeduncular nucleus?
(tectal )
Septal NEP (right) (left)
Superior collicular
al) NEP
(right) Septal NEP (left) Migrating septal neurons
Ventral tegmental area?
c ali ph ce
lic (t ha e e pomotor comple g l x u
Basal telencephalic NEP
t en? m (I I I )
Brain surface (heavier line)
P
o
Ne
l
e
b ic
ica
Posterior commissural GEP
u
s
Lim
rt co
g cin P( NE
e
Primordia lp
c
Posterior commissure
Posterior complex
Dorsal complex
)
T
MESENCEPHALON
Upper medullary NEP M
g in at igr d an
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Labeled on this page: Central neural structures
Spinal nucleus (V)?
Solitary nuclear complex?
LO N HA EP BE NC
Lower rhombic lip Solitary tract
OM
Posterior intramural migratory stream (inferior olive neurons?)
y neurons dullar me
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Lower medullary NEP
RH
g in ttl se
Vestibular nuclear complex?
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
53
PLATE 24A
GW7 Sagittal, CR 18 mm, C1390 Level 4: Slide 9, Section 5
nterior al and a medi o s r Do ll
d sku n an e ski u tur f e Cell sparse Cell-sparse ens ll-d superarachnoid reticulum Ce
LEF TS IDE OF BR A IN
Pia
Cell-dense future dura
me
tri
t
(f
c t)
en
du
cle
se ar sp lle C
m lu cu eti r id no ch ra a r pe su
l and posterior olatera Ventr
ue
Nerve III (oculomotor)
Sella turcica metencephalic pool
Facial ganglion (VII)?
n
Petrous temporal bone
rhombencephalic superventricle
(future fourth ventricle)
g
e ?
Pharynx
u
Otic vesicle
Pa la of tal pr m a oc e x O r a illa ss l c av it T y o
Meckel's cartilage
rv
aq
Mandible
c pe
(o rve I Ne
hypothalamic pool optic recess
Nasal cavity
Maxilla
li
(fu tu
subthalamic pool
Sphenoid bone
Olfactory epithelium
ha
re
ventral pool
Frontonasal process
ep
(future third ventricle)
"Budding" telencephalic choroid plexus foramen of monro
Future frontal bone
nc
pretectal narrows
u
diencephalic superventricle
se
s
do ut su el rs ur p en al e er ce la v p po te e h ol ra nt a l r lic ve ic nt le ri cl e)
thalamic pool
lfactory)
54
Larynx?
Medullary myelencephalic velum pool Incipient rhombencephalic choroid plexus
Spiral ganglion (VIII)
Inferior glossopharyngeal ganglion (IX)? Basal occipital bone
Inferior vagal ganglion (X)?
Vertebral column Dorsal root ganglia
Cell-sparse Cell sparse superarachnoid reticulum
Cell-dense future dura
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-dense future skin and skull
See a high magnification view of the pons and medulla in Plates 28A and B.
PLATE 24B TELENCEPHALON
DIENCEPHALON
MESENCEPHALON
Migrating thalamic neurons Migrating Cajal-Retzius cells and subplate neurons
N
Posterior complex
a
Epithalamic NEP
h
EP
Pretectal NEP
s
(tegmen
ta
e c
n
e s
e M P
NE
Pre o
La te ra l
p ti c An NE ter ior P
P
Facial nerve (VII) genu
nd
Mig rat in g
a
Medial forebrain bundle?
pon ng i l t t se
CTF1 (fibers)
ons neur ti n e
CTF2 (deep nuclear cells) CTF3 (cells and fibers)
Medial cerebellar notch
Pontine NEP
CTF4 (cells)
Cerebellar NEP
Pontomedullary trench
Lateral cerebellar notch
Pontine NEP
Migrating facial motor neurons (VII)?
E
su ne
g c tin i ra am ig thal ns M o ro p u hy ne
Trigeminal nuclear complex (V)?
Upper rhombic lip
Upper medullary NEP
Superior olive complex?
Lower medullary NEP?
Vestibular nuclear complex?
Migrating and settling medullary neurons
Inferior collicular
N
Future optic tract?
P
Migrating preoptic neurons
l NE
Migrating tegmental neurons Migrating isthmal neurons
Hypothalamic ic NEP a m atingmic thal r b ig la s M btha ron Su u
(tectal)
Substantia nigra?
Is t h m a
Migrating basal telencephalic neurons Migrating septal neurons
EP
Basal telencephalic NEP Septal NEP
Superior collicular
alic
N
Olfactory bulb NEP
ph
p
ic
ce
h
al
en
Anterior complex?
Limbic cortical NEP Cingulate/prefrontal?
Brain surface (heavier line)
M e
Dorsal complex
Subicular/ hippocampal
Pioneer migrating pretectal and tectal neurons
Posterior commissural GEP
T
l
ic
a
er lay
a
i c
l)
Primo rdia l pl Neo exi co fo rt r
m
l
m
Posterior commissure
P N E
Solitary nuclear complex Posterior intramural migratory stream (inferior olive neurons?)
So
lit
ar
y
Lower rhombic lip
tr
ac
t
Precerebellar NEP?
Spinal nucleus (V)?
RHOMBENCEPHALON
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase. The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Labeled on this page: Central neural structures
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
55
56
PLATE 25A
GW7 Sagittal, CR 18 mm, C1390 Level 5: Slide 8, Section 8
nterior al and a medi o s r Do
LEF TS IDE OF BR A IN
kull and s skin t u re u f Cell sparse Cell-sparse e ens superarachnoid reticulum ll-d e C Pia
Cell-dense future dura
diencephalic superventricle
future aqueduct
m su es pe en rv ce en ph tr a l ic ic le
(future third ventricle)
subthalamic pool
"Budding" telencephalic choroid plexus
(f
foramen of monro
ventral pool
hypothalamic pool
Nerve III (oculomotor)
Future frontal bone
m lu cu eti r id no ch ra a r pe su rse a sp llCe
Nerve I (olfactory)
Frontonasal process
optic recess Olfactory epithelium Nasal cavity
Sphenoid bone
Nerve V (trigeminal)? Maxilla
rhombencephalic superventricle
Nerve VIII (vestibulocochlear)
(future fourth ventricle)
i
Petrous temporal bone
Meckel's cartilage
Otic vesicle
Mandible
Cell-sparse Cell sparse superarachnoid reticulum
metencephalic pool
Nerve VII (boundary cap*)
Pa la of tal pr m a oc Ora e l c xilla ss av ty
l and posterior olatera Ventr
do t rs ut s u e l al e ur p n po e er ce ol la v p te e h ra n t a l r l ic ve i c nt l e ri cl e)
thalamic pool
Medullary velum
Pharynx
Vestibular ganglion (VIII)
myelencephalic pool
Incipient rhombencephalic choroid plexus Nerve IX and X (boundary caps*) Nerve X (vagus)
Inferior glossopharyngeal ganglion (IX)? Nerve X (vagus)
Occipital bone
Nerve IX (glossopharyngeal) Superior glossopharyngeal ganglion (IX)?
Superior vagal ganglion (X)?
Dorsal root ganglion
* Boundary caps are
Schwann cell GEPs?
Cell sparse superarachnoid reticulum
Cell dense future dura Cell dense future skin and skull
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
See a high magnification view of the pons and medulla in Plates 28A and B.
57
PLATE 25B TELENCEPHALON
DIENCEPHALON
MESENCEPHALON
Migrating thalamic neurons Migrating Cajal-Retzius cells and subplate neurons
m
a l a
Dorsal complex
EP N c
La te ra l
Pre o
An ptic ter ior NEP
t on gp n li
Medial forebrain bundle?
CTF1 (fibers) CTF2 (deep nuclear cells) CTF3 (cells and fibers)
Pontine NEP
CTF4 (cells)
Cerebellar NEP (hemisphere)
Pontomedullary trench
Lateral cerebellar notch
Pontine NEP? Superior olive complex?
Spinal nucleus (V)?
Posterior intramural migratory stream (inferior olive neurons?)
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Labeled on this page: Central neural structures
Upper rhombic lip
Upper medullary NEP
Vestibular nuclear complex?
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
cus?
Medial cerebellar notch
nd Migra tin ga
nis
s ron neu
se tt
in e
lem al ter
al) NE P
La
Facial nerve (VII)
(tect
Migrating inferior collicular neurons
g c tin i ra am ig al s M oth ron p u hy ne
Trigeminal nuclear complex (V)?
lic
ra m ig la s M btha ron su neu
ha
i am g tin ic
Future optic tract?
Migrating and settling medullary neurons
Superior collicular
lar
Migrating preoptic neurons
e
l li c u
Sub
l tha
es
Pioneer migrating pretectal and tectal neurons
co rior Infe
Migrating basal ganglionic neurons
M
lic (tegm cepha en sen tal Me )N g tegmenta n i t EP a r g Mi
Reticular Anterior complex?
Migrating basal telencephalic and olfactory neurons
Pretectal NEP
Posterior commissural GEP
ep
Limbic cortical NEP
Olfactory cortical Basal telencephalic NEP NEP? Anteromedial ganglionic NEP HypoOlfactory bulb thalamic NEP NEP
Brain surface (heavier line)
Epithalamic NEP
nc
co
i Cingulate/ retrosplenial Hippocampal Fornical GEP
h
l
EP
T
i
a
rt
c
N
Posterior commissure
Posterior complex
s ron eu ln
Primord ial p lex ifo rm Ne o
l
er ay
P N E
c
Lower medullary NEP Precerebellar NEP?
Lower rhombic lip
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 26A
GW7 Sagittal, CR 18 mm, C1390 Level 6: Slide 8, Section 2
d anterior ial an med o s r skull Do and skin
re s futu n se e d llCe Cell-dense future dura
LEF TS IDE OF BR A IN
Cell-sparse Cell sparse superarachnoid reticulum
Pia
thalamic pool do t rs ut s u e l al e ur p nc po e e r ol la v e p te e h ra n t a l r l ic ve i c nt l e ri cl e)
diencephalic superventricle (future third ventricle)
l and posterior olatera Ventr
"Budding" telencephalic choroid plexus
(f
58
ventral pool
Future frontal bone Frontonasal process se ar sp lle C
Nasal epithelium
um ul tic re d oi hn ac ar r pe su
Cell-sparse superarachnoid reticulum
Sphenoid bone Nerves VII+VIII (facial +vestibulocochlear) Maxilla
metencephalic pool
rhombencephalic superventricle
Facial ganglion (VII)?
Oral cavity
(future fourth ventricle)
Mandible
Medullary velum
Meckel's cartilage
Pharynx
Vestibular ganglion (VIII)
Otic vesicle
myelencephalic pool
Petrous temporal bone
NerveX (vagus)
Superior vagal ganglion (X)? Basal occipital bone
Cell-sparse Cell sparse superarachnoid reticulum
Cell-dense future dura
Cell-dense future skin and skull
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
PLATE 26B TELENCEPHALON
DIENCEPHALON
MESENCEPHALON
Migrating thalamic/epithalamic neurons GEP (posterior commissure)
i
m
l
E
P
a
on
m
ur
ala
ne
th
ic
am
S
al
us
ti n g
hyp al er at
ot ha
la
su
a mic
bt
h
Brachium of the inferior colliculus
Successive waves of migrating and settling basal ganglionic neurons
CTF1 (fibers)
Medial forebrain bundle? Migrating preoptic neurons
Preoptic NEP
Trigeminal nuclear complex (V)?
eurons ine n ont p g lin
CTF2 (deep nuclear cells) CTF3 (cells and fibers)
ett and s
Migratin g
Lateral lemniscus?
CTF4 (cells)
Medial cerebellar notch
Pontine NEP
Cerebellar NEP (hemisphere) Lateral cerebellar notch
Vestibular nuclear complex?
Migrating and settling medullary neurons
l
Migrating inferior collicular neurons
rea
Future optic tract?
ha
al
collicular
ub
nt
EP al) N ent ons ur
of the stria terminalis?
T
h
N e o c o
ep
al) NE ect (t Inferior
me
c li
s
nc
a lar u lic ol
teg
h
ng
ne
L
ic
se
gm
le B ed nuc
Migrating basal telencephalic and olfactory neurons
N
Migrat i
(te
ra
ig
Olfactory bulb NEP Basal telencephalic NEP
rio rc
Central complex and reticular
ic
Olfactory cortical NEP?
Strionuclear NEP Anteromedial/ anterolateral ganglionic NEP
Anterior complex?
Mese nc Su e pe e
Limbic cortical NEP
Posterior complex Dorsal complex Epithalamic NEP
M
Brain surface (heavier line)
Cingulate/ retrosplenial Hippocampal Fornical GEP
Posterior commissure
p
r
t
i
l
a
lay e
a
c
M
Primordial p lex ifo rm
c
E P
P
P
r
N
E
N
Nucleus of the lateral lemniscus ?
Migrating cochlear nuclear neurons?
Upper rhombic lip
Medullary NEP Auditory (cochlear) NEP
Lower rhombic lip
RHOMBENCEPHALON
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase. The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Labeled on this page: Central neural structures
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
59
PLATE 27A
GW7 Sagittal, CR 18 mm, C1390 Level 7: Slide 6, Section 11 LEF T SID EO FB RA IN
Cell-sparse Cell sparse superarachnoid reticulum
do
r
ri
cl
sa t l ut s u e l po ur p e n ol e er ce la v te e p h ra n t a l r l ic ve i c nt l e
Cell-dense future dura
skin u re fu t se Pia n -de ell
e)
C
erior nd ant ial a d e m l rso sku l and Do
osterior and p teral trola Ven
"Budding" telencephalic choroid plexus
(f ventral pool
se ar sp llCe
Future frontal bone
um ul tic re d oi hn ac ar r pe su
Cell sparse Cell-sparse superarachnoid reticulum
Sphenoid bone
Frontonasal process
Nerve V (trigeminal)
Trigeminal boundary cap*
Trigeminal ganglion (V) metencephalic pool
Facial ganglion and nerve (VII)
Maxilla
rhombencephalic superventricle
(future fourth ventricle)
Oral cavity Mandible
Medullary velum
Ot
Vestibular ganglion (VIII)
ic
Petrous temporal bone
Cell-sparse Cell sparse superarachnoid reticulum
l b on e
Pharynx
le s ic ve
Meckel's cartilage
Cell-dense future skin and skull
oc
ci
pi
ta
Basal occipital bone
Cell-dense future dura
u
s
60
Squamo
* Boundary caps are
Schwann cell GEPs?
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
PLATE 27B TELENCEPHALON
Strionuclear NEP Olfactory Anterolateral cortical NEP? ganglionic NEP
Ventral lateral geniculate?
Me
dia
l genic ul a t e b
o
Migrating subthalamic neurons
Basal telencephalic NEP
Brain surface (heavier line)
Thalamic NEP (posterior complex) ?
Insular cortical Insular? NEP?
Fornical GEP
dy
o
Limbic cortical NEP
late body? icu en
Cingulate/ retrosplenial Hippocampal
g
l
al l Dors ateral
a
Migrating posterior complex thalamic neurons
P N E
r
t
ic
c
N e o
Primordial
plex ifo rm
lay
er
DIENCEPHALON
Bed nucleus of the stria terminalis?
Migrating basal telencephalic and olfactory neurons Successive waves of migrating and settling basal ganglionic neurons
Globus pallidus? CTF1 (fibers) CTF2 (deep nuclear cells)
Central trigeminal tract (devoid of glia)
CTF3 (cells and fibers)
Plentiful glia in peripheral trigeminal nerve and boundary cap*
Trigeminal nuclear complex (V)?
Medial cerebellar notch Trigeminal Cochlear?
Pontine NEP
Cerebellar NEP (hemisphere)
Upper rhombic lip
Lateral cerebellar notch
Lower rhombic lip
RHOMBENCEPHALON
The telencephalic NEP, thalamic NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase. The pontine NEP forms a shrinking shoreline of the superventricle as stockbuilding NEP cells decrease. Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Labeled on this page: Central neural structures
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
61
62
PLATE 28A Level 4: Slide 9, Section 5
See Level 4 in Plates 24A and B. Between Levels 4 and 5: Slide 9, Section 2
Level 5: Slide 8, Section 8
See Level 5 in Plates 25A and B.
GW7 Sagittal, CR 18 mm, C1390
PONS/MEDULLA
PLATE 28B
Facial (VII) and abducens (VI) motor neurons sequestered in superficial Pontine NEP?
t Pon
Pontomedullary trench
in e
ne
Nerve VI (abducens)?
Level 4: Slide 9, Section 5
rhombencephalic superventricle
u oe r
ro Medullary neu
elium p it h
ep
m i t h e li u
Solitary tract?
Medial
Migrating facial (VII) motor neurons?
Lateral
Medullary reticular formation interspersed with other migrating medullary neurons
Nerve VII (facial nerve genu axons are growing laterally)
Predomina
Nerve VI (abducens)?
Nerve VII (facial motor axons are turning ventrally)
ial fibe l superfic n tl y l o n g it u d i n a
r tr a cts
Between Levels 4 and 5: Slide 9, Section 2
ract?
ary t
Migrating facial (VII) motor neurons?
Solit
Migratingand settling superior olive complex and central auditory neurons? Afferent axons from ganglion IX (glossopharyngeal)?
Predomina
ntly longitudinal superficial fiber tracts
le x ? om p ear c l c u rn ibula Vest
Nerve VI (abducens)? Migrating facial (VII) motor neurons?
Solitary tract?
Afferent axons from ganglion IX (glossopharyngeal)?
Nerve VII (facial motor axons exit brain)
Predominantly longit
erficia u din al su p
Nerve VII (Sensory axons from facial ganglion enter brain) Facial nerve boundary cap* * Boundary caps are Schwann cell glioepithelia?
Level 5: Slide 8, Section 8
l fiber
tract
s
Vagal nerve boundary cap*
These arrows indicate the direction of neuronal migration.
Glossopharyngeal nerve boundary cap*
Nerve IX (glossopharyngeal)
Nerve X (vagus)
These arrows indicate the direction of axon growth.
63
64
PART PARTIV: IV: GW7 GW7 HORIZONTAL HORIZONTAL
Carnegie Collection specimen #492 (designated here as C492) was obtained in 1911 after a miscarriage. It has a crown-rump length (CR) of 16.8 mm and is estimated to be at gestational week (GW) 7. C492 was preserved in Zenker’s fixative, embedded in paraffin, and was cut in 40-µm sections that were stained with aluminum cochineal. The dorsal diencephalon and mesencephalic tectum are cut in the horizontal section plane. The plane shifts to predominantly coronal in the anterior telencephalon, ventral diencephalon, pons, and medulla. In general, C492’s sections are cut perpendicular to M2155’s sections (Specimen 1, Part II). We photographed 101 sections at low magnification from the uppermost tip of the pretectum through the spinal cord. Seventeen of these sections are illustrated in Plates 29AB to 45AB. All photographs containing the brain were used to produce computer-aided 3-D reconstructions of the external features of C492’s brain (Figure 3), and to show each illustrated section in situ (insets, Plates 29A to 45A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normalcontrast images) identify non-neural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. A “stockbuilding” telencephalic neuroepithelium surrounds the enlarging telencephalic superventricle. As in other GW7 specimens, few migrating neurons are adjacent to the cortical neuroepithelium while there are many adjacent to the basal ganglionic and basal telencephalic neuroepithelia. The plane of C492’s sections are ideal to show two features of the telencephalic/diencephalic junction that are not seen as clearly in the other GW7 specimens. First, the telencephalic and diencephalic superventricles are continuous at the very wide foramen of Monro. Second, the posterior basal ganglionic neuroepithelium forms a continuum with the ventral diencephalic neuroepithelium, making it difficult to distinguish telencephalic from diencephalic structures.
The “stockbuilding” thalamic neuroepithelium surrounds an expanding thalamic pool in the superventricle, while “shrinking” subthalamic and hypothalamic neuroepithelia surround subthalamic and hypothalamic pools. Many migrating and settling young neurons are in the parenchyma of the future subthalamus and hypothalamus. There are few neurons outside the thalamic neuroepithelium, except in ventral areas where pioneer reticular nuclear neurons are migrating. The roof (tectum and pretectum) of the mesencephalon contains a stockbuilding neuroepithelium adjacent to a very thin layer of pioneer migrating neurons. The bundles of fibers in the posterior commissure are very distinct in the uppermost sections of the pretectum. The tegmental and isthmal neuroepithelia are thinning as their neuronal progeny migrate out, but that thinning is less obvious in C492 compared to other GW7 specimens. Similar to the other GW7 specimens, there is a very thick subpial fiber band; no doubt, these are fibers from sources outside the mesencephalon and isthmus. As in other GW7 specimens, the pons and medulla have neuroepithelia that are shrinking as stem cells unload their neuronal and glial progeny into an expanding parenchyma. For the most part, nuclear subdivisions are indistinct. The superior olivary complex, facial motor nucleus, inferior olivary complex, and solitary nucleus can be tentatively identified. The subpial fiber band is thick and prominent. The “stockbuilding” cerebellar neuroepithelium sharply juts into the lateral part of the rhombencephalic superventricle at the cerebellar notches. The bands of cells and fibers in the cerebellar transitional fields are similar to other GW7 specimens. These bands are prominent in the future hemisphere and are indistinct in the future vermis.
65
C492 Computer-aided 3-D Brain Reconstructions B.
Pretectum
Side view
l l l
a Lower rhombic lip
4. Diencephalic H e m i s p h
Top view
e
r
s
b
r
a
l
S u p e r i o r c o l l i c u l u s
P ons
C o r t e x
Isthmus
C
e
r
e
b
e
l
Figure 3. A, The left side of the 3-D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
Medullary velum
D.
Occipital pole
n
a li g a n g
H
y
l
u
p
lo
a
P
e
B a sal B a s a l
ph
Optic evagination
Lower rhombic lip
e
p
r p e
C ce tele n
a
o
n
m o
t h a l a
Preoptic area
m
p t
u
Olfactory bulb
Scale bars = 1 mm
e
l
w
b
e r
s
S
u
Interhemispheric fissure
r h o mbi c l ip
m e d
x
Upper
Tegmentum
r
e
a
t
m e d u l l
r
s
o
U
a
c
o
r
l
L
Bottom view
Frontal pole
s V e r m i
u
m
m
u
a
l
e
l
P
r
a
E
C
e
h
p
T
u i t h a l a m
Interhemispheric fissure
r e t e c t u m
s
e
Frontal pole
Upper rhombic lip
u
3. Mesencephalic
Occipital pole
l
Medullary velum
2. Pontine
C.
e
d
BRAINSTEM FLEXURES
Lower rhombic lip
m
mus
th e
C
e
b
e
e d u l l a
2
r
M
Mammillary body
M
3
Is
o
Infundibulum
Medullary velum
Inferior colliculus
P
Optic evagination
P o n s
t
u
T
m u s
H
Preoptic area
n
n
u
S
me
la
h
a
Olfactory bulb
e
C
li
t
Basal gang
eg
4
y
m b e l l u
e
Upper rhombic lip
r
Olfactory bulb Preoptic area Optic evagination
a l a m u s
b
Subthalamus
C e r e
T
Ba sa l Basa l te
rebral co Ce
Ist hmus
t
um
nglia ga cephalon len
c o r
x
tum
Inferior colliculus
a l
r
u s a m
egm
e
x te
en
s
Interhemispheric fissure
r
T
u
h
T hal
us am
Occipital pole
lamus tha
Epitha l a l a m
Superior colliculus
Epi
s
Superior colliculus
Pretectum
b
Angled front view
p o t h a
A.
66
PLATE 29A
Level 1: Computer-aided 3-D Brain Reconstruction
GW7 Horizontal CR 16.8 mm C492 Level 1: Section 9
Non-neural structures labeled
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Superarachnoid reticulum (brain parenchymal expansion zone) Pia and pial blood vessels
PLATE 29B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Neural structures labeled Light zone at ventricular border is tangentially cut end feet of NEP cells
Superior collicular primordial plexiform layer Successive waves of migrating superior collicular neurons
Posterior commissure
Wave 1 (oldest neurons) Wave 2 (next oldest neurons)
Columns of migrating pretectal neurons (and glia?)
Uncrossed commissure of the superior colliculus?
mesencephalic superventricle
Posterior commissural GEP?
(future aqueduct)
Roof plate
(future GEP of tectal commissural tracts)
Posterior
Pretectal NEP
(nuclei of the posterior commissure and optic tract?)
(thin, depleted of waves 1 and 2 neuronal precursors)
Anterior
(thick, stockbuilding precursors of neurons) Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
Tectal (superior collicular) NEP
MESENCEPHALIC TECTUM
PRETECTUM
(SUPERIOR COLLICULUS)
MESENCEPHALON
67
68
PLATE 30A
Level 2: Computer-aided 3-D Brain Reconstruction
GW7 Horizontal CR 16.8 mm C492 Level 2: Section 29
Non-neural structures labeled
Dural blood vessels Middle cerebral artery and branches
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Pia and pial blood vessels
Dark stain in some blood vessels is injected ink.
Superarachnoid reticulum (brain parenchymal expansion zone)
PLATE 30B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Neural structures labeled Migrating pretectal neurons
Migrating thalamic neurons
Nucleus of the optic tract?
Thalamic primordial plexiform layer
Superior collicular primordial plexiform layer
Earliest migration wave of thalamic neurons
Migrating superior collicular neurons
diencephalic superventricle (future third ventricle)
mesencephalic superventricle
thalamic pool
Roof plate
(diencephalic)
T
al
Posterior complex (medial geniculate)?
am
Roof plate
i c NEP
(tectal commissural GEP)
Pretectal NEP Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Commissure of the superior colliculus?
pretectal narrows
Posterior complex (dorsal lateral geniculate and pulvinar)?
h
(future aqueduct)
THALAMUS
DIENCEPHALON
PRETECTUM
Tectal (superior collicular) NEP
TECTUM (SUPERIOR COLLICULUS)
MESENCEPHALON 69
70
PLATE 31A GW7 Horizontal CR 16.8 mm C492 Level 3: Section 36 Middle cerebral artery and branches
Anterior cerebral artery and branches
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Dark stain in some blood vessels is injected ink.
Level 3: Computer-aided 3-D Brain Reconstruction Non-neural structures labeled Dural blood vessels Superarachnoid reticulum (brain parenchymal expansion zone) Pia and pial blood vessels
PLATE 31B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Neural structures labeled Successive waves of migrating subthalamic neurons Earliest migration wave of thalamic neurons
Migrating oculomotor nuclear (III) neurons?
Thalamic primordial plexiform layer
Migrating red nuclear neurons? Superior collicular primordial plexiform layer
Mesencephalic reticular formation?
Cortical primordial plexiform layer
Migrating superior collicular neurons
Migrating Cajal-Retzius cells and subplate neurons
mesencephalic superventricle
diencephalic superventricle thalamic pool
Roof plate
(diencephalic)
TELENCEPHALON CEREBRAL CORTEX
subthalamic pool
Dorsal/central complexes?
Th
Commissure of the superior colliculus
(future aqueduct)
(future third ventricle)
Tegmental NEP Interpeduncular NEP? Oculomotor (III) NEP?
al
Reticular
am
Ventral complex?
ic
NE
P ( t h i ck
Rubral NEP?
) Roof plate
(mesencephalic commissural GEP) Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
Subthalamic NEP (thin) THALAMUS
SUBTHALAMUS
DIENCEPHALON
Tectal (superior collicular) NEP TEGMENTUM
TECTUM
MESENCEPHALON 71
72
PLATE 32A GW7 Horizontal CR 16.8 mm C492 Level 4: Section 39 Middle cerebral artery and branches
Anterior cerebral artery and branches
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Dark stain in some blood vessels is injected ink.
Level 4: Computer-aided 3-D Brain Reconstruction Non-neural structures labeled Dural blood vessels Superarachnoid reticulum (brain parenchymal expansion zone) Pia and pial blood vessels
PLATE 32B
Neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Migrating mammillary neurons Migrating subthalamic neurons Earliest migration wave of thalamic neurons Thalamic primordial plexiform layer
Migrating interpeduncular nuclear neurons Mesencephalic reticular formation? Migrating oculomotor nuclear (III) neurons? Migrating red nuclear nucleus neurons?
Cortical primordial plexiform layer
Migrating substantia nigra neurons? neurons Superior collicular primordial plexiform layer
Migrating Cajal-Retzius cells and subplate neurons
Migrating superior collicular neurons
Medial lemniscus and medial forebrain bundle?
Commissure of the superior colliculus? mesencephalic superventricle
diencephalic superventricle
(future aqueduct)
(future third ventricle)
Roof plate (diencephalic) telencephalic superventricle
Tegmental NEP
Interpeduncular? Oculomotor (III)?
Central complex?
(very thick due to tangential cut)
am
Ventral complex?
ic
NE
P ( thic k)
Roof plate
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
THALAMUS
SUBTHALAMUS
CEREBRAL CORTEX
TELENCEPHALON
Substantia nigra and ventral tegmental area?
DIENCEPHALON
(mesencephalic commissural GEP)
TEGMENTUM
Neocortical NEP
al
Hypothalamic (mammillary) NEP (thick) Subthalamic NEP (thin)
(mammillary body)
Th
Rubral? Reticular
HYPOTHALAMUS
(future lateral ventricle, posterodorsal pool)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
(thick and thin areas)
subthalamic pool and mammillary recess
thalamic pool
Tectal (superior collicular) NEP (thick) TECTUM
MESENCEPHALON 73
74
PLATE 33A GW7 Horizontal CR 16.8 mm C492 Level 5: Section 45
Level 5: Computer-aided 3-D Brain Reconstruction Non-neural structures labeled Dural blood vessels Pia and pial blood vessels
Middle cerebral artery and branches
Anterior cerebral artery and branches
Superarachnoid reticulum (brain parenchymal expansion zone)
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Interpeduncular fossa
Dark stain in some blood vessels is injected ink.
PLATE 33B
Neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating mammillary neurons
Migrating ventral tegmental area neurons Pioneer exiting oculomotor nerve (III) fibers
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)?
Migrating oculomotor nucleus (III) neurons
Medial lemniscus and medial forebrain bundle
Sprouting oculomotor nerve (III) fibers
Migrating subthalamic neurons
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Earliest migration wave of thalamic neurons
Migrating substantia nigra and ventral tegmental area neurons?
Thalamic primordial plexiform layer
Cortical primordial plexiform layer
Migrating inferior collicular neurons? Tectal primordial plexiform layer
Migrating Cajal-Retzius cells and subplate neurons
Migrating superior collicular neurons Commissure of the superior colliculus?
subthalamic pool
diencephalic superventricle
Roof plate (diencephalic)
(future third ventricle, Ante thalamic pool) rio
mesencephalic superventricle
mammillary recess
(future aqueduct)
Roof plate
(mesencephalic)
r
Cingulate
or
al
po ol )
h
Ce
a
Retrosplenial
nt
r al
la m
ic
Ve nt
r al
NE P
ar
T
Re ti c
NEP
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
Hypothalamic (mammillary) NEP Subthalamic NEP
THALAMUS
DIENCEPHALON
HYPOTHALAMUS (mammillary body)
ic
bi
SUBTHALAMUS
co
rt
m
ul
(CEREBRAL CORTEX)
Fo rn Hi ic pp al oc G cc te EP a s l m ve up en o pa n t (f e r c t r e u ri t v p ic a l cl u e h e, r e n a lN po la tr lic EP st te ic er ra le i l
Li
Neo
TELENCEPHALON
Raphe complex Oculomotor (III)?
Superior collicular
Substantia nigra/ ventral tegmental area?
Tegmental NEP
Inferior collicular Tectal NEP
TEGMENTUM
TECTUM
MESENCEPHALON
75
76
PLATE 34A GW7 Horizontal CR 16.8 mm C492 Level 6: Section 50
Level 6: Computer-aided 3-D Brain Reconstruction Non-neural structures labeled Dural blood vessels Pia and pial blood vessels
Middle cerebral artery and branches
Anterior cerebral artery and branches
Superarachnoid reticulum (brain parenchymal expansion zone)
Superior sagittal sinus?
Primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Circle of Willis arteries? Dark stain in some blood vessels is injected ink.
PLATE 34B
Neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medial forebrain bundle? Migrating subthalamic neurons (zona incerta, Forel's fields) Settling subthalamic nuclear neurons? Migratory waves of thalamic neurons Thalamic primordial plexiform layer
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)? Migrating mammillary neurons Migrating raphe, ventral tegmental area, substantia nigra, and oculomotor (III) neurons Medial lemniscus? Mesencephalic reticular formation? Sprouting oculomotor nerve (III) fibers
Cortical primordial plexiform layer
Migrating inferior collicular neurons?
Migrating Cajal-Retzius cells and subplate neurons
Tectal primordial plexiform layer Migrating superior collicular neurons
Fornical GEP Telencephalic stem cells of choroid plexus
Commissure of the superior colliculus?
Roof plate (diencephalic,
subhypothalamic pools
Fornical GEP
diencephalic superventricle
stem cells of choroid plexus)
T
Ce
Li e pp m oc bi t am (f s el c pa ut u e c l or ur pe nc t e r e Re i c po la v p a st te en ha l N tros er ra t l E P p le n io l ri ic ia l r ve c ? po nt le ol ri ) cl e,
o
h
n tr
r
ti c a l
Re t
N E P
NEP
Subthalamic NEP
THALAMUS Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
(mammillary?)
i
N E P
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
al
Ven al t r al am ic
(mesencephalic)
mesencephalic superventricle (future aqueduct)
Hypothalamic Substantia nigra/ ventral tegmental area?
Tegmental NEP HYPOTHALAMUS
Hi
SUBTHALAMUS
at
la r
ul
c
(CEREBRAL CORTEX)
o N e
TELENCEPHALON
ng
Oculomotor (III)?
cu
Ci
Roof plate
Raphe complex?
or
(future third ventricle, thalamic pool) Anteri
DIENCEPHALON
Superior collicular
Inferior collicular
Tectal NEP
TEGMENTUM
TECTUM
MESENCEPHALON
77
78
PLATE 35A GW7 Horizontal CR 16.8 mm C492 Level 7: Section 55
Level 7: Computer-aided 3-D Brain Reconstruction Non-neural and peripheral neural structures labeled Dural blood vessels
Middle cerebral artery and branches
Pia and pial blood vessels
Pia and pial blood vessels Anterior cerebral artery and branches Superior sagittal sinus?
Superarachnoid reticulum (brain parenchymal expansion zone)
Primordial mesenchymal brain case (skin/bone) Nerve III (oculomotor) Dark stain in some blood vessels is injected ink.
Future dura (internal border of brain case)
Circle of Willis arteries?
PLATE 35B
Central neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)?
Medial forebrain bundle? Migratory waves of subthalamic neurons
Migrating raphe, ventral tegmental area, substantia nigra, and oculomotor (III) neurons Mesencephalic reticular formation?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Cortical primordial plexiform layer
Sprouting oculomotor nerve (III) fibers? Migrating inferior collicular neurons?
Migrating Cajal-Retzius cells and subplate neurons
Tectal primordial plexiform layer
Fornical GEP
telencephalic superventricle
(future lateral ventricle, posterior pool)
Migrating superior collicular neurons
Telencephalic stem cells of choroid plexus
TH ng
Li
N e
bi
Hi
e
cc
or
o
c
(CEREBRAL CORTEX)
m
at
o
TELENCEPHALON
ul
r
t i c a l
pp
tic
AL
AM
oc
am p Pa al ra hi pp
al
NE
oc
P
am
pa
SU Subthalamic BT HA NEP LA MU S
(future aqueduct)
Oculomotor (III)?
Hypothalamic NEP PO HY
Substantia nigra/ ventral tegmental area? Superior collicular
Tegmental NEP Inferior collicular
N E P
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
mesencephalic superventricle
(mesencephalic)
Premammillary Middle
US
l?
Roof plate
Raphe complex?
A M US
Ci
diencephalic superventricle
(future third ventricle, thalamic pool)
AL
Anterior thalamic NEP
stem cells of choroid plexus)
TH
Roof plate (diencephalic,
hypothalamic pool
Fornical GEP
Tectal NEP
TEGMENTUM Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
DIENCEPHALON
TECTUM
MESENCEPHALON
79
80
PLATE 36A
Level 8: Computer-aided 3-D Brain Reconstruction Non-neural and peripheral neural structures labeled
GW7 Horizontal CR 16.8 mm C492, Level 8: Section 65
Middle cerebral artery Dural blood vessels
Pia and pial blood vessels
Posterior cerebral artery
Branches of anterior cerebral artery Superior sagittal sinus?
Superarachnoid reticulum (brain parenchymal expansion zone)
Cerebellar artery?
Vascular bed of choroid plexus
Nerve III (oculomotor) Circle of Willis arteries?
Primordial mesenchymal brain case (skin/bone) Dark stain in some blood vessels is injected ink.
Future dura (internal border of brain case)
Central neural structures labeled
PLATE 36B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating middle hypothalamic neurons
Migrating isthmal neurons
Migrating subthalamic neurons?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Sprouting oculomotor (III) nerve? mesencephalic superventricle (future aqueduct, isthmal canal)
Migrating Cajal-Retzius cells and subplate neurons
Cortical primordial plexiform layer
Medial forebrain bundle?
Lateral lemniscus and brachium of inferior colliculus
Migrating bed nucleus of the stria terminalis neurons?
Migrating inferior collicular neurons
telencephalic superventricle
(future lateral ventricle, posterior pool) Stem cells of choroid plexus
Raphe glial structure GEP in mesencephalic floor plate
Telencephalic
Limbic cortical NEP
L
Amygdaloid/posterior ganglionic NEP
N
C
e
O R
T
E
o X
c
o
r t i c a l
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
N E P
(mesencephalic) Diencephalic floor plate?
Su bt h NE ala SU P? mic BA BT SA LG HA AN LA GL MU S? IA
C E R E B R A L
ic lam a h ot yp EP h le N dd TH Mi PO HY
US
Strionuclear NEP
Roof plate
M
Hippocampal Cingulate
diencephalic superventricle
(future third ventricle, hypothalamic pool)
Isthmal NEP
LA
A B R C E R E
Fornical GEP
fo ra m mo of en nr o
Diencephalic
A
Junction of telencephalic and diencephalic roof plates
Tectal (inferior collicular) NEP
X T E C O R
DIENCEPHALON Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
ISTHMUS
TECTUM
MESENCEPHALON
TELENCEPHALON
81
82
PLATE 37A GW7 Horizontal CR 16.8 mm C492, Level 9: Section 71
Level 9: Computer-aided 3-D Brain Reconstruction Non-neural and peripheral neural structures labeled Pia and pial blood vessels Middle cerebral artery
Dural blood vessels
Superior sagittal sinus? Superarachnoid reticulum (brain parenchymal expansion zone) Cerebellar artery?
Vascular bed of choroid plexus
Primordial mesenchymal brain case (skin/bone) Dark stain in some blood vessels is injected ink.
Basilar artery? Nerve III (oculomotor) Future dura (internal border of brain case)
Circle of Willis arteries?
Central neural structures labeled
PLATE 37B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Migrating arcuate nuclear neurons? Migrating and settling posterior hypothalamic neurons
Migrating isthmal neurons
Migrating and settling anterior hypothalamic neurons
Cortical primordial plexiform layer
mesencephalic superventricle
Migrating Cajal-Retzius cells and subplate neurons
(future aqueduct, isthmal canal)
Sprouting trochlear nerve (IV) fibers?
posterior pool
telencephalic superventricle
Medial forebrain bundle?
(future lateral ventricle)
Migrating trochlear (IV) neurons?
Migrating amygdaloid/ posterior ganglionic neurons?
anterior pool
Stem cells of choroid plexus
Migrating bed nucleus of the stria terminalis neurons?
Telencephalic
Junction of telencephalic and diencephalic roof plates
fo ra me n
L
C
O
R
of mo nr o
Amygdaloid/posterior ganglionic NEP
N
A
e
o T
Anterior hypothalamic NEP G AN GL IA
o r t i c a l X
Middle hypothalamic NEP
HYPOTHALAMUS
DIENCEPHALON
c E
(mesencephalic)
(future third ventricle, hypothalamic pool)
Strionuclear NEP
Limbic cortical NEP
Roof plate
Diencephalic floor plate?
BA S A L
BR C E R E
Cingulate
Lateral lemniscus
diencephalic superventricle
Diencephalic
Fornical GEP Hippocampal
Migrating inferior collicular neurons?
Raphe glial structure GEP in mesencephalic floor plate
N E P C E R E B R A L
TELENCEPHALON
RT C O
E
Isthmal NEP
ISTHMUS
Tectal (inferior collicular?) NEP
TECTUM?
MESENCEPHALON
X
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
83
84
PLATE 38A
Non-neural structures labeled Pia and pial blood vessels Posterior cerebral artery Internal carotid artery Dural blood vessels Middle cerebral artery
GW7 Horizontal CR 16.8 mm C492, Level 10: Section 87
Level 10: Computer-aided 3-D Brain Reconstruction
Cerebellar artery?
Superior sagittal sinus?
Superarachnoid reticulum (brain parenchymal expansion zone)
Dural blood vessels Primordial mesenchymal brain case (skin/bone)
Dark stain in some blood vessels is injected ink.
Future dura (internal border of brain case)
Circle of Willis arteries?
Basilar artery?
PLATE 38B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating arcuate nuclear neurons?
Successive migratory waves of basal ganglionic neurons
2 Future putamen?
3
Layers of the cerebellar transitional field (CTF)
Central trigeminal tract?
Medial forebrain bundle?
Migrating trigeminal (V) neurons? Migrating raphe and abducens (VI) neurons?
telencephalic superventricle
Sprouting abducens nerve (VI)?
(future lateral ventricle) anterior pool
CT F2: Mig rati CTF ng d 1 eep nu c l e a CT F3
ons ur
rn e
1
Migrating CajalRetzius cells and subplate neurons
Lateral hypothalamic neuron migration?
Future pallidum?
Cortical primordial plexiform layer
Migrating middle hypothalamic neurons?
Po n fo tine rm r at etic io u n? la r
Migrating neurons originating in corticoganglionic NEP
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Neural structures labeled
Damaged area in section
cor tic
Insular
al
NE
P
CEREBRAL CORTEX
Limbic cortical NEP
Anteromedial
Cortico ganglionic AnteroNEP lateral
Posterior Lateral?
Middle
H y pot h
TELENCEPHALON
ar
In f u n d
ic N E P a l am
Raphe glial structure
rhombencephalic superventricle
(future fourth ventricle) Metencephalic roof plate splits into paired upper rhombic lips
Raphe complex?
Medullary velum
Abducens (VI)? Reticular formation? Trigeminal (V)
G
BASAL GANGLIA
ul
EP
Diencephalic floor plate? Raphe glial structural GEP in pontine floor plate
ib
(future third ventricle) hypothalamic pool
N
Neo
Hippocampal Cingulate
diencephalic superventricle
f of ora mo me Fornical nr n o GEP
an g l i onic
Subfornical organ primordium in telencephalic roof plate
infundibular recess
Medial lemniscus?
Pontine NEP
HYPOTHALAMUS
PONS
DIENCEPHALON Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Cerebellar NEP Medial cerebellar notch
CEREBELLUM
RHOMBENCEPHALON Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
85
86
PLATE 39A GW7 Horizontal CR 16.8 mm C492 Level 11: Section 94 Superior sagittal sinus?
Non-neural structures labeled Internal carotid artery Middle cerebral artery
Maxillary process
Circle of Willis arteries? Basilar artery? Posterior cerebral artery
Superarachnoid reticulum (brain parenchymal expansion zone)
Frontonasal process?
Pia and pial blood vessels
Primordial mesenchymal brain case (skin/bone)
Dark stain in some blood vessels is injected ink.
Level 11: Computer-aided 3-D Brain Reconstruction
Future dura (internal border of brain case)
Dural blood vessels
Neural structures labeled
PLATE 39B
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Successive migratory waves of basal ganglionic/basal telencephalic neurons
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Layers of the cerebellar transitional field (CTF)
telencephalic superventricle
(future lateral ventricle) Migrating basal telencephalic neurons originating in limbic cortical NEP
Migrating CajalRetzius cells and subplate neurons
Medial forebrain bundle?
1
CTF4-5 (cells-deep neurons) Migrating abducens (VI) and premigratory facial (VII) motor neurons?
2
ca
l
EP
G
Cortical (olfactory) NEP
al
u lar
infundibular recess
In f u n d
hal pot a m i c N E Hy
P
te r
(future fourth ventricle) Metencephalic roof plate splits into paired upper rhombic lips
Raphe glial Raphe structural GEP in pontine complex? floor plate
Medullary velum
Abducens (VI)?
enc
Facial motor (VII)? Reticular formation?
s ba
Fu
t ur
e
BASAL GANGLIA AND BASAL TELENCEPHALON
TELENCEPHALON
La
le Midd
ep h
F tu re pallu idum ? alo n
P
rhombencephalic superventricle
Raphe glial structure
te l
An
c o r ti
Anterolateral
NE
(future third ventricle, hypothalamic pool)
Sprouting abducens (VI) and facial (VII) nerve fibers?
al
bic
Insular
en o r amon r fo f m o
tero m an g l i o edial nic Future putamen?
Li
m Cingulate/ prefrontal
diencephalic superventricle
r r io s te Po
Septal NEP
Diencephalic floor plate?
3
anterior pool
Subfornical organ primordium in telencephalic roof plate
Medial lemniscus?
ib
ol f re act ce or ss y
Premigratory Purkinje neurons sequestered in superficial cerebellar NEP
Longitudinal domains of migrating and settling pontine neurons
Ret icu lar for ma tion
Lateral hypothalamic neuron migration?
CEREBRAL CORTEX
CTF2 (cells-deep neurons)
Migrating middle hypothalamic neurons?
Cortical primordial plexiform layer
N
CTF1 (fibers)
Migrating arcuate nuclear neurons?
Pontine NEP Cerebellar NEP
HYPOTHALAMUS
DIENCEPHALON
Medial cerebellar notch
PONS
Lateral cerebellar notch?
CEREBELLUM
RHOMBENCEPHALON Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
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88
PLATE 40A
Peripheral neural and non-neural structures labeled Nerve V (trigeminal, boundary cap*) Nerve V (trigeminal, sensory) Nerve V (trigeminal, motor) Circle of Willis arteries?
GW7 Horizontal CR 16.8 mm C492 Middle cerebral/carotid artery Level 12: Section 112
Posterior cerebral artery
* Boundary caps are Schwann cell GEPs?
Level 12: Computer-aided 3-D Brain Reconstruction
Nerve II (optic) Zygomatic bone? Nerve I (olfactory) Olfactory epithelium Nasal septum Medullary velum
Nerve VI (abducens)?
Superarachnoid reticulum (brain parenchymal expansion zone) Hypothetical olfactory induction field
Pia and pial blood vessels
Eye
Pigment epithelium Retinal NEP Vitreous body Intraretinal space Sclera Dark stain in some blood vessels is injected ink.
Sella turcica in sphenoid bone
Primordial mesenchymal brain case (skin/bone)
Future dura and dural blood vessels (internal border of brain case)
PLATE 40B
Central neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Layers of the cerebellar transitional field (CTF)
CTF1 (fibers)
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
CTF2 (cells-deep neurons) CTF4-5 (cells-deep neurons)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
CTF6 (cells-Purkinje cells) Migrating trigeminal (V) sensory neurons? Central trigeminal fibers Migrating arcuate nucleus neurons? Settling trigeminal motor (V) neurons? Migrating anterior hypothalamic neurons?
Metencephalic roof plate splits into paired upper rhombic lips
optic recess
Medial
infundibular recess preoptic recess
Preoptic area Germinal zones
PREOPTIC AREA
Migrating median preoptic nuclear neurons?
Preoptic NEP Chiasmal GEP
Infundibular NEP Posterior pituitary GEP in diencephalic floor plate
Anterior NEP
rhombencephalic superventricle
Ret formicular ation
diencephalic superventricle
(future third ventricle, hypothalamic/ preoptic pool)
Raphe glial lemniscus? structure
Lateral hypothalamic neurons?
Longitudinal domains of migrating and settling pontine neurons
Medial forebrain bundle?
(future fourth ventricle)
Raphe glial structure GEP in pontine floor plate Raphe complex? Abducens (VI) and facial motor (VII)?
Sprouting abducens (VI) and facial (VII) nerve fibers?
Medullary velum
Pontine NEPs
Reticular formation?
Migrating abducens (VI) and premigratory facial (VII) motor neurons?
Trigeminal (V)?
Hypothalamic Germinal zones HYPOTHALAMUS
Cerebellar NEP Metencephalic roof plate splits into paired upper rhombic lips
Medial
DIENCEPHALON
Lateral
PONS
Cerebellar notches
CEREBELLUM
RHOMBENCEPHALON
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
89
90
PLATE 41A
Peripheral neural and non-neural structures labeled Nerve V (trigeminal, sensory) Nerve V (trigeminal, motor) Trigeminal (V) ganglion
GW7 Horizontal CR 16.8 mm C492 Level 13: Section 118
Nerve V (trigeminal, boundary cap*) Future dura and dural blood vessels (internal border of brain case) Posterior cerebral artery Pia and pial blood vessels
Level 13: Computer-aided 3-D Brain Reconstruction
Olfactory epithelium Nerve I (olfactory) Nasal cavity
Nasal septum
Ethmoid bone?
Sphenoid bone?
Frontonasal process?
C ar aro te tid ry ?
Superarachnoid reticulum (brain parenchymal expansion zone) ica Sella turc
Or bit o-s ph en oid pr oc ess ?
Neurohypophysis Adenohypophysis
Pituitary gland
Hypothetical olfactory induction field
Nerve VII (boundary cap?*)
Eye
Sprouting optic nerve (II) fibers Retinal NEP Pigment epithalium Vitreous body Cornea Lens Pioneer retinal ganglion cells Intraretinal space Sclera
* Boundary caps are
Schwann cell GEPs?
Primordial mesenchymal brain case (skin/bone)
Dark stain in some blood vessels is injected ink.
PLATE 41B
Central neural structures labeled Metencephalic roof plate splits into paired upper rhombic lips
Migrating cochlear nuclear neurons?
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating trigeminal (V) sensory neurons?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Settling trigeminal motor (V) neurons?
Peripheral trigeminal (V) axons have more interstitial glia than central axons.
Trigeminal nerve (V) motor axons have fewer interstitial glia than sensory axons. Longitudinal domains of migrating and settling pontine reticular formation neurons Migrating arcuate nuclear neurons? Medial Raphe glial lemniscus? structure
Pioneer optic tract fibers?
Migrating suprachiasmatic nucleus neurons?
diencephalic superventricle
(future third ventricle, hypothalamic pool, infundibular recess)
Chiasmal GEP
Infundibular NEP Posterior pituitary GEP in diencephalic floor plate
Hypothalamic Germinal zones
(future fourth ventricle)
Superior olive? Migrating abducens (VI) and premigratory facial motor (VII) neurons? Raphe glial structure GEP in pontine floor plate Raphe complex?
Sprouting abducens (VI) nerve fibers?
Abducens (VI), facial motor (VII), and reticular formation?
Trigeminal (V)? Auditory (cochlear)
DIENCEPHALON Central trigeminal fibers Lateral\ lemniscus?
PONS
Medullary velum
Pontine NEPs
Sprouting facial (VII) nerve fibers?
HYPOTHALAMUS
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
rhombencephalic superventricle
Facial motor nucleus?
Metencephalic roof plate splits into paired upper rhombic lips
Cerebellar NEP Medial Lateral Cerebellar notches
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
CEREBELLUM
RHOMBENCEPHALON
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
91
92
PLATE 42A GW7 Horizontal CR 16.8 mm C492 Level 14: Section 141
Peripheral neural and non-neural structures labeled Nerve VIII (vestibulocochlear, boundary cap*) Nerve VIII (vestibulocochlear) Vestibular (VIII) ganglion
Squamous temporal bone
Level 14: Computer-aided 3-D Brain Reconstruction
Future dura and dural blood vessels (internal border of brain case)
Superarachnoid reticulum (brain parenchymal expansion zone)
avit al c y Or
Pia and pial blood vessels
Tongue
M an dib le
Basilar artery
a
le
Sphenoid bone?
M
ib nd
Palatal process
Petrous temporal bone
Maxillary sinus?
Maxilla
tid ro y? Ca rter a
Maxillary sinus?
* Boundary caps are
Schwann cell GEPs?
Primordial mesenchymal brain case (skin/bone)
Dark stain in some blood vessels is injected ink.
PLATE 42B
Central neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Myelencephalic roof plate splits into paired lower rhombic lips Migrating cochlear nuclear neurons? Lateral lemniscus?
Migrating vestibular neurons?
mati on
Settling facial motor nucleus (VII) neurons?
rhombencephalic superventricle
ar fo r
Longitudinal domains of migrating and settling pontomedullary neurons
ticu l
Superior olive?
Re
Medial lemniscus?
(future fourth ventricle)
Prepositus nucleus?
Raphe glial structure
Raphe complex NEP?
Medullary velum
Raphe glial structure GEP in floor plate
Medial longitudinal fasciculus?
Prepositus nuclear and reticular formation NEP
Spinal nucleus and tract (V)? Vestibular NEP
Pontomedullary germinal zones
Auditory (cochlear) NEP Myelencephalic roof plate splits into paired lower rhombic lips
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
LOWER PONS/UPPER MEDULLA
RHOMBENCEPHALON
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
93
94
PLATE 43A
Peripheral neural and non-neural structures labeled
Petrous temporal bone
GW7 Horizontal CR 16.8 mm C492 Level 15: Section 152
Level 15: Computer-aided 3-D Brain Reconstruction
Squamous temporal bone Future dura and dural blood vessels (internal border of brain case)
Basilar artery
c avity
Basal occipital bone?
a Or l
Future hyoid bone?
Tongue
Sublingual salivary gland? Meckel's cartilage (mandibular process)
tid ro y? Ca rter a
Pia and pial blood vessels Superarachnoid reticulum (brain parenchymal expansion zone)
Dark stain in some blood vessels is injected ink.
Temporal bone labyrinth (future cochlea, utricule, saccule, and semicircular canals)
Primordial mesenchymal brain case (skin/bone) Vestibulocochlear nerve (VIII) boundary cap (Schwann cell GEP?)
Central neural structures labeled
PLATE 43B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Myelencephalic roof plate splits into paired lower rhombic lips
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Premigratory precerebellar nuclear neurons?
Posterior intramural migratory stream (inferior olive neurons)? Migrating vestibular neurons?
Longitudinal domains of migrating and settling medullary neurons Inferior olive?
Medial lemniscus? Medial longitudinal fasciculus? Raphe glial structure
Hypoglossal (XII) nucleus? Vagal motor (X) nucleus?
rhombencephalic superventricle
(future fourth ventricle)
Re
Hypoglossal nuclear (XII), vagal motor (X), and reticular formation NEP
tic ar ul n io at rm fo
Spinal nucleus and tract (V)?
Raphe complex NEP
Medullary velum
Medullary germinal zones
Raphe glial structure GEP in medullary floor plate Vestibular NEP? Precerebellar NEP
Myelencephalic roof plate splits into paired lower rhombic lips Lateral lemniscus?
MEDULLA
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
95
96
PLATE 44A
Peripheral neural and non-neural structures labeled
GW7 Horizontal CR 16.8 mm C492 Level 16: Section 169
Petrous temporal bone
Basilar artery
cavit y
Basal occipital bone
ral
Tongue
tid ro y? Ca rter a
Internal auditory meatus?
Level 16: Computer-aided 3-D Brain Reconstruction
Future dura (internal border of brain case)
O
Primordium of larynx?
Pia and pial blood vessels
Squamous temporal bone
Ve r
teb
r al
arte
ry?
Primordial mesenchymal brain case (skin/bone)
External ear?
Vagal nerve (X) boundary cap (Schwann cell GEP?) Nerve X (vagal) Dark stain in some blood vessels is injected ink.
Superarachnoid reticulum (brain parenchymal expansion zone)
Superior vagal (X) ganglion
PLATE 44B
Central neural structures labeled
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Myelencephalic roof plate splits into paired lower rhombic lips
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Densely packed premigratory precerebellar nuclear neurons? Few interstitial glia in central fiber tracts Abundant interstitial glia in peripheral nerve
rhombencephalic superventricle
(future fourth ventricle)
Migrating vestibular neurons? Posterior intramural migratory stream (inferior olive neurons)?
Hypoglossal (XII) nucleus?
Medullary velum
Vagal motor (X) nucleus?
Inferior olive? Medial longitudinal fasciculus? Raphe glial structure
Hypoglossal nucleus (XII), vagal motor (X), and reticular formation NEP
Medial lemniscus decussation? Medial lemniscus? Spinocerebellar tracts in inferior cerebellar peduncle?
Reticular formation
Solitary nucleus and tract
Raphe complex NEP Raphe glial structure GEP in medullary floor plate Solitary nuclear NEP
Medullary germinal zones
Visceral sensory afferent fiber tracts? Precerebellar NEP Myelencephalic roof plate splits into paired lower rhombic lips
LOWER MEDULLA
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
97
98
PLATE 45A
Peripheral neural and non-neural structures labeled
GW7 Horizontal CR 16.8 mm C492 Level 17: Section 205
Dorsal root ganglia
Squamous occipital bone
Level 17: Computer-aided 3-D Brain Reconstruction
Traces of nerve XII (hypoglossal)? Pia and pial blood vessels Future dura (internal border of brain case)
Spinal nerve (dorsal roots) Dorsal root boundary caps
Vertebral column
Primordial mesenchymal brain case (skin/bone) Superior vagal (X) ganglion Superarachnoid reticulum (brain parenchymal expansion zone) Dark stain in some blood vessels is injected ink.
Central neural structures labeled
PLATE 45B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Abundant interstitial glia in peripheral nerve
Densely packed premigratory precerebellar nuclear neurons?
Dorsal sensory nucleus (X)?
Myelencephalic roof plate splits into paired lower rhombic lips
Dorsal motor nucleus (X)? Hypoglossal nucleus (XII)? Posterior intramural migratory stream (inferior olive neurons)?
rhombencephalic superventricle
Dorsal funiculus Few interstitial glia in central fiber tracts
Dorsal gray
(future fourth ventricle)
Inferior olive?
Medullary velum
Medial longitudinal fasciculus? Raphe glial structure
Hypoglossal nuclear (XII), vagal motor (X), and reticular formation NEP Raphe complex NEP
Reticular formation Solitary nucleus and tract Spinocerebellar tracts in inferior cerebellar peduncle?
SPINAL CORD
Raphe glial structure GEP in medullary floor plate Solitary nuclear and vagal sensory (X) NEP Precerebellar NEP
Medullary germinal zones Myelencephalic roof plate splits into paired lower rhombic lips
LOWER MEDULLA
RHOMBENCEPHALON Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
99
100
PART PARTV: V: GW6.5 GW6.5 CORONAL CORONAL
This specimen is embryo #2051 in the Minot Collection, designated here as M2051. The crown-rump length (CR) is 15 mm estimated to be at gestational week (GW) 6.5. Most of M2051’s brain sections are cut (10 µm) in the coronal plane, but the plane shifts to predominantly horizontal in the posterior medulla. We photographed 87 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and medulla. Seventeen of these sections are illustrated in Plates 46AB to 62AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of M2051’s brain (Figure 4), and to show each illustrated section in situ (insets, Plates 46A to 62A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. Plates 63AB show a high-magnification view of the neocortical neuroepithelium. All parts of the telencephalic neuroepithelium are rapidly increasing their pool of neuronal and glial stem cells as they expand the shorelines of the enlarging telencephalic superventricle. Only very few pioneer Cajal-Retzius neurons have migrated into the cell-sparse primordial plexiform layer adjacent to the cerebral cortical neuroepithelium. The rest of the cortical neuronal population has yet to be generated. The basal ganglionic and basal telencephalic neuroepithelia, although increasing their stock of stem cells, do have adjacent migrating neurons. There are many fewer neurons in these areas than in the GW7 specimens (Parts II, III, and IV). As in the GW7 specimens, these neurons appear to migrate together in early (outermost and less dense) to late (innermost and most dense) waves. The diencephalic neuroepithelium surrounds a narrowing superventricle. It is thinnest in the hypothalamic and subthalamic areas, where it is surrounded by denselypacked waves of migrating neurons. It is postulated that these areas of the superventricle have shrinking shorelines
as the neuroepithelia “unload” their stock of neuronal precursors. In contrast, the superventricle shoreline is still expanding as the thalamic neuroepithelium continues to add more neuronal precursors than to unload postmitotic neurons. There are only a few neurons migrating outside the thalamic neuroepithelium. The mesencephalon contains a stockbuilding neuroepithelium in the pretectum and tectum (relatively few adjacent migrating neurons). On the other hand, the tegmental and isthmal neuroepithelia are thinner. Migrating neurons are leaving in large numbers and accumulate in clumps so dense that the superficial border of the neuroepithelium is indistinct. Some cells lie farther out in the tegmental and isthmal parenchyma and are more sparsely scattered adjacent to the subpial fiber band. Both the pons and medulla have neuroepithelia that are thicker than at GW7, but are nevertheless shrinking as they unloaded their neuronal and glial progeny into an expanding parenchyma. Cells are migrating and settling in longitudinal arrays at the pontine flexure. A few cells are settling in the faintly discernable superior olivary complex and many are settling in the reticular formation throughout the pons and medulla. Some facial motor neurons are migrating from medial to lateral, leaving behind their axons in a small, but definite genu of the facial nerve. Migrating inferior olive neurons are in the posterior intramural migratory stream outside the precerebellar neuroepithelium in the posterior lower rhombic lip, but very few neurons have settled in the inferior olive. Many neurons have settled in the solitary nucleus, surrounding a definite solitary tract. The cerebellar neuroepithelium is in the stockbuilding phase, mainly adding precursors of Purkinje cells and some late-generated deep nuclear neurons. Many deep nuclear neurons are migrating in the cellular layers of the cerebellar transitional field, but these and the fibrous layers are thinner and less definite than at GW7.
101
M2051 Computer-aided 3-D Brain Reconstructions B.
Side view
b
C e r e
m
b e l l u
Ba
B
Upper rhombic lip
as
sal ganglia on al al t e l e nce p h
H
e
Preoptic area
r
C
e
Optic evagination
Preoptic area Optic evagination
3 C
e
hm r
e
b
e
u l l
2
Mammillary body
Lower rhombic lip
M e d u
Ist
Upper rhombic lip
Medullary velum
Infundibulum
Medullary velum
P o n s
Inferior colliculus
y
T Subthalamus
Ba Ba s a l s al t el e
rebral co Ce
x t e
Ist hmus
4
o
m tu
c
eg me n
a l
r
Inferior colliculus
ia gl a n alon g eph nc
Interhemispheric fissure
us am
r
t u m e n
u s
r
x te
T
u s
h a l a
e g m
m
T
us am
Occipital pole
T
m
Epitha l
Superior colliculus
m
Angled front view
Pretectum Epit ha l l a ha
s
Superior colliculus
u
Pretectum
Su bthalam us p o t h a l a n s m u s P o
A.
M
a l l
BRAINSTEM FLEXURES
e
d u l l a
1
1. Medullary
Lower rhombic lip
2. Pontine Spinal cord
3. Mesencephalic Spinal cord
4. Diencephalic
C.
Top view
H e m i s p h e r
e
m
u
s
e
C o r t e x
Isthmus
ns
r a l
S u p e r i o r c o l l i c u l u s
Po
b
V e r m i s
a
P
r
l
p
e
a
E
C
T h
m
Interhemispheric fissure
u
Frontal pole
i t h a l a m
u
r e t e c t u m
s
Occipital pole
Figure 4. A, The left side of the 3-D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
C
e
b
e
r
e
l
l
Upper rhombic lip
D.
Medullary velum
Scale bars = 1 mm
Optic evagination
lip
a
l
l
m e d u
r al Co
in
p
S
w
m e d u l l a
ic
o
a
li
mb
e r
p
P o n s
y
U
n ga
g
H
rho
e r p p
lo
n
B a s a l
ha
t h a l a
C B asal telencep
o
e
S
Preoptic area
p t u
s
e r e
m
Interhemispheric fissure
er
L
Occipital pole Tegmentum
u
Frontal pole
l
m
b
r
a
Low
d
Bottom view
r t e x c o
102
PLATE 46A GW6.5 Coronal CR 15.0 mm M2051 Level 1: Section 66
Non-neural structures labeled Interhemispheric fissure Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Pia
Level 1: Computer-aided 3-D Brain Reconstruction
Frontonasal process Naso-optic furrow Placodal epithelium Medial nasal process
PLATE 46B
Neural structures labeled
TELENCEPHALON
The dorsomedial neocortical primordial plexiform layer contains even fewer cells.
EP Nanterodorsal (future lateral ventricle)
Few migrating Cajal-Retzius cells are outside the lateral neocortical NEP.
ic
co
r tical NE
P
Cingulate
anteroventral pool
Insular
Brain surface (heavier line)
pool
telencephalic superventricle
Neocorti
ca
l
CEREBRAL CORTEX
Lim
b
Prefrontal
More migrating Cajal-Retzius cells are in the primordial plexiform layer outside the ventrolateral limbic cortical NEP. Few migrating Cajal-Retzius cells outside ventromedial limbic cortical NEP
The density of migrating cells in the primordial plexiform layer indicates ventrolateral-todorsomedial and ventrolateral-to-ventromedial maturation gradients in the cerebral cortex.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
103
104
PLATE 47A GW6.5 Coronal CR 15.0 mm M2051 Level 2: Section 107
Non-neural and peripheral neural structures labeled Interhemispheric fissure Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Pia
Frontonasal process
Level 2: Computer-aided 3-D Brain Reconstruction
Naso-optic furrow Olfactory epithelium Nasal epithelium Placodal epithelium Nasal septum
Medial nasal process Nostril opening to nasal cavity Lateral nasal process
105
PLATE 47B
Central neural structures labeled
TELENCEPHALON CEREBRAL CORTEX
Hippocampal Cingulate
Limbic cortical NEP
Brain surface (heavier line) Cortical primordial plexiform layer
anterodorsal pool
Neocortical NEP
Fornical GEP Limbic cortical (insular) NEP
Migrating Cajal-Retzius cells More migrating cells adjacent to insular NEP indicate earlier maturation.
telencephalic superventricle
Corticoganglionic NEP?
(future lateral ventricle)
Anterolateral ganglionic NEP
anteroventral pool
Roof plate
Migrating neurons originating in the corticoganglionic NEP?
(telencephalic stem cells of choroid plexus)
Migrating pioneer basal ganglionic neurons
Basal telencephalic NEP Septal NEP
BASAL GANGLIA/ BASAL TELENCEPHALON
Migrating pioneer basal telencephalic neurons
Migrating medial septal neurons FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
106
PLATE 48A GW6.5 Coronal CR 15.0 mm M2051 Level 3: Section 130
Non-neural and peripheral neural structures labeled Interhemispheric fissure Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
See a high-magnification view of the cerebral cortex in Section 122 in Plates 63A and B.
Future dura (internal border of brain case)
Pia
Frontal sinus? Hypothetical olfactory induction field Nerve I (olfactory)
Naso-optic furrow Frontonasal process Olfactory epithelium Nasal epithelium
Lateral nasal process Nostril opening to nasal cavity
Level 3: Computer-aided 3-D Brain Reconstruction
Placodal epithelium Medial Nasal septum nasal process
The GW6 Face and Neck
Figure 247D modified (Patten, 1953, p. 429.)
Nasal septum
Frontal prominence
Medial nasal process Naso-optic furrow Lateral nasal process Nostril Mouth Hyoid arch (II)
Hyoid bone
Eye Maxillary process Mandibular arch (I) Hyo-mandibular cleft Laryngeal cartilages Mandible
107
PLATE 48B Central neural structures labeled Roof plate
(telencephalicdiencephalic junction)
TELENCEPHALON CEREBRAL CORTEX
Limbic cortical NEP
Hippocampal Cingulate
Brain surface (heavier line) Cortical primordial plexiform layer
Corticoganglionic NEP?
Anterolateral ganglionic NEP
anterodorsal pool Telencephalic
Migrating Cajal-Retzius cells More migrating cells adjacent to insular NEP indicate earlier maturation.
Diencephalic future third ventricle (diencephalic roof)
e (futur
Limbic cortical (insular) NEP
Fornical GEP
c ephali telenc entricle le) v ventric supelr ateral
Neocortical NEP
anteroventral pool
Stem cells of choroid plexus
Migrating neurons originating in the corticoganglionic NEP?
foramen of monro
Migrating pioneer basal ganglionic neurons
Basal telencephalic (olfactory?) NEP Septal NEP
BASAL GANGLIA/ BASAL TELENCEPHALON
Migrating pioneer basal telencephalic neurons
Migrating medial septal neurons
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
108
PLATE 49A GW6.5 Coronal CR 15.0 mm M2051 Level 4: Section 159
Non-neural and peripheral neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Vascular bed of choroid plexus
Pia
Orbito-sphenoid process? Naso-optic furrow Hypothetical olfactory induction field Sclera of eye Nerve I (olfactory)
Olfactory epithelium Nasal cavity Maxillary process Placodal epithelium
Nasal septum Nasal epithelium Medial nasal process Lateral nasal process
Level 4: Computer-aided 3-D Brain Reconstruction
109
PLATE 49B
Central neural structures labeled
DIENCEPHALON THALAMUS
Roof plate
Dorsal complex
Thalamic NEP
(diencephalic stem cells of choroid plexus?)
Reticular nucleus
Migrating pioneer thalamic neurons
Anterior complex
Thalamic primordial plexiform layer
TELENCEPHALON CEREBRAL CORTEX Hippocampal Cingulate
Brain surface (heavier line)
(thalamic pool)
Neocortical NEP
diencephalic superventricle
Limbic cortical NEP
Fornical GEP dorsal pool
Cortical primordial plexiform layer
tu
l ic e e ) ha cl ic l ep ri t r nc nt v e n le ve l te per t e r a a sure l
(f u
Migrating Cajal-Retzius cells
Limbic cortical (insular) NEP Corticoganglionic NEP?
Anterolateral ganglionic NEP Basal telencephalic (olfactory?) NEP Septal NEP
ventral pool
Roof plate
More migrating cells adjacent to insular NEP indicate earlier maturation.
(telencephalic stem cells of choroid plexus)
Migrating neurons originating in the corticoganglionic NEP?
foramen of monro
Successive waves of migrating basal ganglionic neurons
Anteromedial ganglionic NEP
BASAL GANGLIA/ BASAL TELENCEPHALON Migrating pioneer basal telencephalic neurons
Migrating medial septal neurons
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
110
PLATE 50A GW6.5 Coronal CR 15.0 mm M2051 Level 5: Section 190
Non-neural and peripheral neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Vascular bed of choroid plexus
Pia
Nerve I (olfactory) Naso-optic furrow
Eye Pigment epithelium Intraretinal space Vitreous body Retinal NEP Sclera
Lens of eye
Olfactory epithelium Nasal cavity
Nasal septum
Maxillary process Nasal epithelium Placodal epithelium Oral cavity Medial nasal process Lateral nasal process
Level 5: Computer-aided 3-D Brain Reconstruction
Mandibular process
111
EPITHALAMUS THALAMUS
PLATE 50B
Central neural structures labeled
DIENCEPHALON
Roof plate
Epithalamic (habenular) NEP?
(primordium of pineal gland)
Migrating pioneer epithalamic/ thalamic neurons
Posterior complex?
Thalamic primordial plexiform layer
Ventral complex?
Thalamic NEP
Reticular nuclear Anterior complex epithalamic/ thalamic pool
Limbic cortical NEP
Hippocampal Cingulate/ retrosplenial
Limbic cortical (insular) NEP Corticoganglionic NEP?
telencephali c superv
Neocortical NEP
(future late entricle ral ventricl e) posterior pool
Fornical GEP
Anterolateral ganglionic NEP Anteromedial ganglionic NEP
foramen of monro
Brain surface (heavier line)
(future third ventricle)
CEREBRAL CORTEX
diencephalic superventricle
TELENCEPHALON
preoptic pool
Basal telencephalic NEP
Cortical primordial plexiform layer
Roof plate
(telencephalic stem cells of choroid plexus)
bus Glolidus? l a p
Migrating Cajal-Retzius cells More migrating cells adjacent to lateral cortical NEP indicate earlier maturation.
Migrating neurons originating in the corticoganglionic NEP? Successive waves of migrating basal ganglionic neurons
BASAL GANGLIA/ BASAL TELENCEPHALON
Successive waves of migrating basal telencephalic neurons
DIENCEPHALON PREOPTIC AREA
Preoptic NEP Migrating preoptic area neurons
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
112
PLATE 51A GW6.5 Coronal CR 15.0 mm M2051 Level 6: Section 241
Non-neural and peripheral neural structures labeled
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Pia
Orbito-sphenoid process? Pial blood vessels
Eye
Intraretinal space Pigment epithelium Retinal NEP Pioneer retinal ganglion cells Vitreous body Sclera
Naso-optic furrow Nerve II (optic)
Ethmoid bone? Oral cavity
optic recess
Tongue
Anterior cardinal vein? Maxillary process Palatal process
Mandibular process
Level 6: Computer-aided 3-D Brain Reconstruction
113
PLATE 51B
Central neural structures labeled MESENCEPHALON
Roof plate
PRETECTUM?
(posterior commissural GEP?)
Migrating pretectal neurons?
Pretectal NEP?
Brain surface (heavier line)
DIENCEPHALON
mesencephalic superventricle?
THALAMUS
(future aqueduct)
Posterior complex?
Thalamic NEP
Thalamic primordial plexiform layer
Ventral complex?
diencephalic superventricle
(future third ventricle)
SUBTHALAMUS
Subthalamic NEP TELENCEPHALON
CEREBRAL CORTEX
Neocortical NEP telencephalic superventricle
Migrating pioneer thalamic neurons
thalamic pool
Reticular nuclear
posterior pool
(future lateral ventricle)
Migrating reticular nuclear neurons? Migrating subthalamic (Forel's fields, zona incerta) neurons? Cortical primordial plexiform layer Migrating Cajal-Retzius cells
subthalamic pool
Limbic cortical NEP Amygdaloid NEP
AMYGDALA
Strionuclear NEP?
DIENCEPHALON
Lateral area
PREOPTIC AREA Preoptic NEP
preoptic pool
Migrating amygdaloid neurons Migrating bed nucleus of the stria terminalis neurons? Migrating lateral preoptic neurons Migrating medial preoptic neurons
Medial area
Chiasmal channel? Optic nerve (II) GEP Preoptic NEP bordering optic recess Chiasmal GEP
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
114
PLATE 52A GW6.5 Coronal CR 15.0 mm M2051 Level 7: Section 258
Non-neural and peripheral neural structures labeled
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Cell-dense primordial mesenchymal brain case (skin/bone) Dural blood vessels
Future dura (internal border of brain case) Pia
Pial blood vessels
Orbito-sphenoid process? Naso-optic furrow
Eye Pigment epithelium Intraretinal space Retinal NEP Sclera
Sphenoid bone? Oral cavity Tongue
Anterior cardinal vein? Maxillary process Palatal process
Meckel's cartilage
Mandibular process Hypoglossal nerve (XII)?
Level 7: Computer-aided 3-D Brain Reconstruction
115
PLATE 52B
Central neural structures labeled MESENCEPHALON PRETECTUM
Roof plate
(posterior commissural GEP?)
Posterior commissure
Pretectal NEP
Migrating pretectal neurons mesencephalic superventricle?
DIENCEPHALON
(future aqueduct)
Posterior complex (lateral geniculate and pulvinar)?
Thalamic NEP
thalamic pool
(future third ventricle)
Ventral complex?
diencephalic superventricle
THALAMUS
Reticular nuclear
TELENCEPHALON
CEREBRAL CORTEX
Neocortical NEP telencephalic superventricle
(future lateral ventricle, posterior pool)
Thalamic primordial plexiform layer
Migrating pioneer thalamic neurons
Migrating reticular nuclear neurons? Cortical primordial plexiform layer Migrating Cajal-Retzius cells
subthalamic pool
Migrating subthalamic (Forel's fields, zona incerta) neurons?
DIENCEPHALON SUBTHALAMUS
Subthalamic NEP
Migrating lateral preoptic neurons Lateral area
PREOPTIC AREA
Brain surface (heavier line)
preoptic pool
Preoptic NEP Medial area
Trajectory of future optic nerve (II)
optic recess
Optic nerve (II) and chiasmal GEP
Suprachiasmatic NEP?
HYPOTHALAMUS
Anterobasal NEP?
Migrating suprachiasmatic neurons? Migrating anterobasal neurons?
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
116
PLATE 53A GW6.5 Coronal CR 15.0 mm M2051 Level 8: Section 285
Non-neural and peripheral neural structures labeled
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Dural blood vessels
Pia
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Pial blood vessels
Ali-sphenoid process? Anterior pituitary gland Sphenoid bone? Maxillary process
Oral cavity Tongue
Anterior cardinal vein? Palatal process Meckel's cartilage
Mandibular process Hypoglossal nerve (XII)?
Level 8: Computer-aided 3-D Brain Reconstruction
PLATE 53B
Central neural structures labeled
MESENCEPHALON PRETECTUM
Roof plate
(posterior commissural GEP?)
Posterior commissure
Pretectal NEP
DIENCEPHALON THALAMUS
(future aqueduct)
Posterior complex (lateral geniculate and pulvinar)?
(future third ventricle)
thalamic pool
Ventral complex?
diencephalic superventricle
Thalamic NEP
Migrating pretectal neurons mesencephalic superventricle?
Posterior complex (medial geniculate)? Reticular nuclear
SUBTHALAMUS
Subthalamic NEP
subthalamic pool
HYPOTHALAMUS
Lateral
Dorsal
Hypothalamic NEP
Brain surface (heavier line)
Thalamic primordial plexiform layer
Migrating pioneer thalamic neurons
Migrating reticular nuclear neurons?
Migrating subthalamic neurons (Forel's fields, zona incerta)?
Migrating lateral hypothalamic neurons? hypothalamic pool
Migrating dorsal hypothalamic neurons?
Anterior
infundibular recess
Migrating anterior hypothalamic neurons? Medial forebrain bundle?
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
117
118
PLATE 54A
Non-neural and peripheral neural structures labeled
GW6.5 Coronal CR 15.0 mm M2051 Level 9: Section 330
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) Dural blood vessels
Pia Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Pituitary gland
Ali-sphenoid process?
Posterior (neurohypophysis) Anterior (adenohypophysis)
Sphenoid bone (sella turcica)
Trigeminal ganglion (V) Nerve V (trigeminal) Eustachian tube? Oral cavity Tongue
Palatal bone?
Lingual epithelium Palatal process
Level 9: Computer-aided 3-D Brain Reconstruction
Anterior cardinal vein? Maxillary process
Mandibular process Maxillary-mandibular placodal epithelium
119
PLATE 54B
Central neural structures labeled Roof plate
MESENCEPHALON
(posterior commissural GEP?)
PRETECTUM
Pretectal NEP mesencephalic superventricle?
DIENCEPHALON THALAMUS
(future aqueduct)
Posterior complex (lateral geniculate and pulvinar)? thalamic pool
(future third ventricle)
Ventral complex?
diencephalic superventricle
Thalamic NEP
Posterior complex (medial geniculate)? Reticular nuclear
SUBTHALAMUS
Subthalamic NEP
subthalamic pool
HYPOTHALAMUS
Hypothalamic NEP
Lateral
Anterior/dorsal
Posterior commissure Migrating pretectal neurons Light areas are pockets of sprouting pretectal and thalamic axons Thalamic primordial plexiform layer Successive waves of migrating thalamic neurons separated by sprouting axons
Migrating reticular nuclear neurons? Brain surface (heavier line)
Migrating subthalamic neurons (Forel's fields, zona incerta)? Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)?
Migrating lateral hypothalamic neurons? hypothalamic pool infundibular recess
Middle/infundibular
Medial forebrain bundle? Migrating dorsal and anterior hypothalamic neurons? Migrating middle hypothalamic neurons? Migrating arcuate nuclear neurons?
Median eminence/ neurohypophysis (pituicyte) GEP
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
120
PLATE 55A GW6.5 Coronal CR 15.0 mm M2051 Level 10: Section 357
Non-neural and peripheral neural structures labeled
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Dural blood vessels
Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Middle cerebral artery? Circle of Willis artery? Pontine artery? Sphenoid bone Posterior cerebral artery? Nerve V (trigeminal) Trigeminal ganglion (V) Anterior cardinal vein?
Basilar artery
Basal occipital bone
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Level 10: Computer-aided 3-D Brain Reconstruction
Otic vesicle
Facial ganglion (VII)? Petrous temporal bone
Nerve VII (facial)?
121
PLATE 55B
Central neural structures labeled Roof plate
MESENCEPHALON
(posterior commissural GEP?)
PRETECTUM
Posterior commissure
Pretectal NEP
Pretectal primordial plexiform layer Successive waves of migrating pretectal neurons separated by sprouting axons
mesencephalic superventricle (future aqueduct)
TEGMENTUM
Mesencephalic reticular formation?
Rubral?
Tegmental NEP
Migrating red nuclear neurons? Oculomotor (III)?
Migrating oculomotor (III) nuclear neurons?
Interpeduncular?
Brain surface (heavier line)
DIENCEPHALON SUBTHALAMUS
subthalamic pool
Lateral
Hypothalamic NEP Middle
diencephalic superventricle
HYPOTHALAMUS
Medial forebrain bundle?
(future third ventricle)
Subthalamic NEP
Migrating subthalamic neurons (Forel's fields, zona incerta)? Migrating lateral hypothalamic neurons? Luysian migration (subthalamic nuclear neurons originating in hypothalamic NEP)?
hypothalamic pool
Migrating arcuate nuclear neurons? Floor plate (diencephalic)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
122
PLATE 56A GW6.5 Coronal CR 15.0 mm M2051 Level 11: Section 384
Non-neural and peripheral neural structures labeled
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Dural blood vessels
Future dura (internal border of brain case) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Middle cerebral artery? Circle of Willis artery?
* Boundary caps are
Schwann cell GEPs? Trigeminal boundary cap* Facial boundary cap* Facial ganglion (VII)?
Nerve VII (facial)? Vestibular ganglion (VIII)
Temporal bone labyrinth (otic vesicle) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Basilar artery Basal occipital bone
Level 11: Computer-aided 3-D Brain Reconstruction
Petrous temporal bone
Spiral ganglion (VIII) budding from otic vesicle epithelium?
Anterior cardinal vein?
123
TECTUM
PLATE 56B
Central neural structures labeled
MESENCEPHALON
Roof plate
Posterior commissure?
(posterior commissural GEP?)
Tectal primordial plexiform layer
Superior collicular NEP mesencephalic superventricle
Successive waves of migrating superior collicular neurons separated by sprouting axons
(future aqueduct)
Migrating red nuclear neurons?
TEGMENTUM Rubral?
Tegmental NEP
Mesencephalic reticular formation?
Oculomotor?
Migrating oculomotor (III) nuclear neurons? Migrating interpeduncular nucleus neurons?
Interpeduncular?
DIENCEPHALON
HYPOTHALAMUS
diencephalic superventricle (mammillary recess)
Brain surface (heavier line)
Hypothalamic NEP (posterior, mammillary)
Luysian migration (subthalamic nucleus neurons originating in hypothalamic NEP)?
Floor plates
PONS Central trigeminal tract?
Diencephalic Pontine (raphe glial structure GEP)
Longitudinal domains of migrating and settling pontine neurons
Trigeminal (V) nuclear complex
Pontine reticular formation
Migrating raphe nuclear complex neurons Caudal extension of trigeminal nuclear complex?
RHOMBENCEPHALON Midline raphe glial structure Medial lemniscus?
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
124
PLATE 57A
Non-neural and peripheral neural structures labeled
GW6.5 Coronal CR 15.0 mm M2051 Level 12: Section 420
Pia
Cell-dense primordial mesenchymal brain case (skin/bone)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Circle of Willis arteries? Basilar artery
Vestibolocochlear boundary cap (Schwann cell GEP?)
Petrous temporal bone
Temporal bone labyrinth (otic vesicle)
Basilar artery
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Superior glossopharyngeal ganglion (IX)? Basal occipital bone?
Level 12: Computer-aided 3-D Brain Reconstruction
125
PLATE 57B
Central neural structures labeled MESENCEPHALON
Commissure of the superior colliculus?
Roof plate
(commissural GEP?)
TECTUM
Tectal primordial plexiform layer
Superior collicular NEP
Migrating superior collicular neurons Brain surface (heavier line)
mesencephalic superventricle (future aqueduct)
TEGMENTUM Mesencephalic reticular formation?
Substantia nigra?
Tegmental NEP
Migrating substantia nigra neurons?
Ventral tegmental area? Oculomotor (III)?
Migrating oculomotor (III) nuclear neurons? Migrating ventral tegmental area neurons?
DIENCEPHALON
HYPOTHALAMUS (mammillary body) PONS
Pontine floor plate
(raphe glial structure GEP)
rhombencephalic superventricle
(future fourth ventricle)
Medial pontine NEP
Midline raphe glial structure Medial lemniscus? Migrating raphe nuclear complex neurons Pontine reticular formation
Lateral pontine NEP
Trigeminal (V) nuclear complex?
CEREBELLUM
Migrating deep nuclear neurons?
Cerebellar NEP Migrating cochlear nuclear neurons? Nucleus of the lateral lemniscus?
Auditory (cochlear?) NEP Lateral medullary NEP
Lateral lemniscus?
Nerve VII (genu)?
Medullary reticular formation
Settling facial motor nuclear neurons (VII)? Medial medullary NEP
Medial longitudinal fasciculus? Medullary floor plate
(raphe glial structure GEP)
Spinal nucleus (V)? Premigratory facial motor nuclear neurons (VII)? Abducens nucleus (VI)? Superior olivary complex? Migrating raphe nuclear complex neurons Medial lemniscus? Midline raphe glial structure
MEDULLA
RHOMBENCEPHALON Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
126
PLATE 58A
Non-neural and peripheral neural structures labeled
GW6.5 Coronal CR 15.0 mm M2051 Level 13: Section 438
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) with blood vessels
Nerve III sheath (oculomotor) Basilar artery
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Vestibolocochlear boundary cap (Schwann cell GEP?) Temporal bone labyrinth (otic vesicle)
Petrous temporal bone
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Basilar artery
Level 13: Computer-aided 3-D Brain Reconstruction
Glossopharyngeal ganglion (IX) Vagal ganglion (X) Basal occipital bone? Foramen magnum?
127
Central neural structures labeled
PLATE 58B
Commissure of the superior colliculus?
Roof plate
(commissural GEP?)
Migrating superior collicular neurons
MESENCEPHALON TECTUM
Tectal primordial plexiform layer
mesencephalic superventricle
Superior collicular NEP
(future aqueduct)
Inferior collicular NEP?
Migrating inferior collicular neurons Brain surface (heavier line)
TEGMENTUM
Tegmental NEP
Substantia nigra?
Migrating substantia nigra neurons?
Ventral tegmental area?
Migrating oculomotor (III) nuclear neurons?
Oculomotor (III)?
Migrating ventral tegmental area neurons?
Midline raphe glial structure Medial lemniscus?
PONS
Pontine floor plate
Migrating raphe nuclear complex neurons
(raphe glial structure GEP)
Medial pontine NEP
(raphe nuclei and reticular formation?)
CTF1 (fibers)
Pontine reticular formation
Layers of the cerebellar transitional field (CTF)
CTF2 (cells-deep neurons) CTF3 (fibers)
CEREBELLUM
CTF4-5 (cells-deep neurons?)
Medial cerebellar notch
metencephalic pool
Cerebellar NEP (hemisphere)
Upper (pontine roof plate)
rhombencephalic superventricle (future fourth ventricle)
Lower (medullary roof plate)
myelencephalic pool
Auditory NEP
Segregating rhombic lips
Migrating cochlear nuclear neurons? Nucleus of the lateral lemniscus?
(cochlear?)
Lateral medullary NEP (vestibular nuclear complex?)
Medullary reticular formation
Medial medullary NEP
(reticular formation, raphe nuclei and prepositus nucleus?)
Lateral lemniscus? Spinal nucleus (V)? Migrating vestibular nuclear neurons? Prepositus nucleus?
Medial longitudinal fasciculus? Medullary floor plate
MEDULLA
(raphe glial structure GEP)
Raphe nuclear complex? Medial lemniscus? Midline raphe glial structure
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
128
PLATE 59A
Non-neural and peripheral neural structures labeled
GW6.5 Coronal CR 15.0 mm M2051 Level 14: Section 488
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Temporal bone labyrinth (otic vesicle)
Squamous temporal bone Petrous temporal bone
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Trajectory of nerve XII (hypoglossal)?
Level 14: Computer-aided 3-D Brain Reconstruction
Superior vagal ganglion (X)? Squamous occipital bone?
129
Central neural structures labeled Roof plate (commissural GEP?) MESENCEPHALON
PLATE 59B
Commissure of the superior colliculus?
Migrating superior collicular neurons
TECTUM
"Cave in" here is a processing artifact.
Superior collicular NEP
Tectal primordial plexiform layer
mesencephalic superventricle
Brain surface (heavier line)
(future aqueduct)
Inferior collicular NEP?
Migrating inferior collicular neurons
TEGMENTUM
Tegmental NEP
Substantia nigra?
Migrating substantia nigra and ventral tegmental area neurons?
Ventral tegmental area? Oculomotor (III)?
Medial longitudinal fasciculus?
isthmal canal
ISTHMUS
Migrating isthmal neurons
Isthmal NEP
Layers of the cerebellar transitional field (CTF) CTF1 (fibers)
CEREBELLUM
CTF2 (cells-deep neurons) CTF3 (fibers) CTF4-5 (cells-deep neurons?)
isthmal canal
Cerebellar NEP metencephalic pool
Metencephalic roof plate (upper rhombic lip)
Lateral cerebellar notch
Medial cerebellar notch rhombencephalic superventricle (future fourth ventricle)
Myelencephalic roof plate
Medullary velum
myelencephalic pool
(lower rhombic lip)
Posterior intramural migratory stream (inferior olive neurons)?
Precerebellar nuclear NEP
Migrating vestibular nuclear neurons?
Lateral medullary NEP
Medullary reticular formation
(vestibular nuclear complex?)
Solitary nucleus and tract?
Medial medullary NEP
(reticular formation, raphe nuclei and prepositus nucleus?)
Medial longitudinal fasciculus?
MEDULLA
Medullary floor plate
(raphe glial structure GEP)
Settling inferior olive neurons? Raphe nuclear complex? Medial lemniscus? Midline raphe glial structure
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
130
PLATE 60A
Non-neural and peripheral neural structures labeled
GW6.5 Coronal CR 15.0 mm M2051 Level 15: Section 553
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Level 15: Computer-aided 3-D Brain Reconstruction Squamous occipital/ temporal bones?
Trajectory of nerve X (vagus)?
Superior vagal ganglion (X)?
131
Central neural structures labeled
Roof plate
MESENCEPHALON
PLATE 60B
Commissure of the superior colliculus?
(commissural GEP?)
Migrating superior collicular neurons
TECTUM
"Cave in" here is a processing artifact.
Superior collicular NEP
Tectal primordial plexiform layer Brain surface (heavier line)
mesencephalic superventricle (future aqueduct)
Inferior collicular NEP
Migrating isthmal neurons
ISTHMUS
Isthmal NEP
Layers of the cerebellar transitional field (CTF)
isthmal canal
CTF1 (fibers)
CEREBELLUM
CTF2 (cells-deep neurons) CTF3 (fibers)
Cerebellar NEP
CTF4-5 (cells-deep neurons?)
Medial cerebellar notch
metencephalic pool
Metencephalic roof plate
Lateral cerebellar notch
(dorsal rhombic lip)
Medullary velum rhombencephalic superventricle (future fourth ventricle)
These folds are processing artifacts.
MEDULLA
Myelencephalic roof plate
myelencephalic pool
(ventral rhombic lip)
Migrating precerebellar nuclear neurons? Precerebellar nuclear NEP
Migrating vestibular nuclear neurons?
Lateral medullary NEP
Solitary nucleus and tract
(vestibular/solitary nuclear complexes?)
Medial medullary NEP
(reticular formation, raphe complex, hypoglossal [XII] and vagal motor [X] nuclei?)
Medullary reticular formation
Medial longitudinal fasciculus? Medullary floor plate (raphe glial structure GEP)
Migrating hypoglossal and vagal motor nuclear neurons? Raphe nuclear complex Medial lemniscus decussation?
RHOMBENCEPHALON SPINAL CORD
Spinal floor plate
(raphe glial structure GEP)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Posteior intramural migratory stream (inferior olive neurons)? Settling inferior olive neurons?
Midline raphe glial structure Ventral funiculus Ventral gray
Ventral spinal NEP
FONT KEY: ventricular divisions - capitals Intermediate spinal NEP Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Dorsal spinal NEP Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons. Spinal roof plate
Intermediate gray Lateral funiculus Dorsal gray Dorsal funiculus
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
132
PLATE 61A GW6.5 Coronal CR 15.0 mm M2051 Level 16: Section 583
Non-neural structures labeled
Pia
Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Superarachnoid reticulum (brain parenchymal expansion zone)
Level 16: Computer-aided 3-D Brain Reconstruction
Future dura (internal border of brain case)
133
PLATE 61B
Neural structures labeled MESENCEPHALON
Migrating superior colliculus neurons
Roof plate
TECTUM
(commissural GEP?)
Superior collicular NEP
Tectal primordial plexiform layer
"Cave in" here is a processing artifact.
Brain surface (heavier line)
mesencephalic superventricle (future aqueduct)
Inferior collicular NEP
isthmal canal
ISTHMUS
Trochlear (IV) nucleus Nerve IV (trochlear)
Trochlear nuclear NEP
CEREBELLUM
Layers of the cerebellar transitional field (CTF)
Vermis
Cerebellar NEP
CTF1 (fibers) CTF2 (cells-deep neurons)
Intermediate hemisphere
Medial cerebellar notch
Lateral hemisphere
CTF4-5 (cells-deep neurons?)
metencephalic pool
Lateral cerebellar notch
Metencephalic roof plate (upper rhombic lip)
rhombencephalic superventricle (future fourth ventricle)
Medullary velum
These folds are processing artifacts.
Myelencephalic roof plate
myelencephalic pool
(lower rhombic lip)
Migrating precerebellar nuclear neurons?
Precerebellar nuclear NEP Lateral medullary NEP
Solitary nucleus and tract
(solitary nuclear complex and sensory vagal [X] nuclei?)
Medial medullary NEP
(reticular formation, raphe nuclear complex, hypoglossal (XII) and vagal motor (X) nuclei?)
Medullary reticular formation
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Posteior intramural migratory stream (inferior olive neurons)? Migrating hypoglossal (XII) and vagal motor (X) nuclear neurons? Raphe nuclear complex
SPINAL CORD Intermediate spinal NEP
Dorsal spinal NEP Spinal roof plate
Lateral funiculus Intermediate gray Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
134
PLATE 62A GW6.5 Coronal CR 15.0 mm M2051 Level 17: Section 643
Non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Level 17: Computer-aided 3-D Brain Reconstruction
Pia
135
PLATE 62B Neural structures labeled MESENCEPHALON POSTERIOR TIP OF TECTUM Brain surface (heavier line)
RHOMBENCEPHALON CEREBELLUM
Layers of the cerebellar transitional field (CTF) CTF1 (fibers)
Cerebellar NEP (vermis)
CTF2 (cells-deep neurons) metencephalic pool
CTF4-5 (cells-deep neurons?)
Metencephalic roof plate (upper rhombic lip)
Medullary velum The infolding of the medullary velum and overlying brain case primordium is an artifact of shrinkage during histological processing.
rhombencephalic superventricle
(future fourth ventricle)
MEDULLA
Myelencephalic roof plate (lower rhombic lip)
Migrating precerebellar nuclear neurons?
Precerebellar nuclear NEP? Migrating cuneate nuclear neurons?
Lateral medullary NEP (cuneate nucleus?)
myelencephalic pool
Migrating gracile nuclear neurons? Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Posterior medullary NEP (gracile nucleus?)
Medullary roof plate
RHOMBENCEPHALON FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
See Level 3 in Plates 48A and B.
CEREBRAL CORTEX FUTURE PARACENTRAL LOBULE
136
PLATE 63A GW6.5 Coronal, CR 15.0 mm, M2051 Near Level 3: Section 122
PLATE 63B Pia Brain surface (heavier line)
Neocortical primordial plexiform layer Earliest migrating Cajal-Retzius cells Synthetic zone of pseudostratified NEP
Neocortical NEP
(in "stockbuilding" stage when more NEP cells are being added and few neurons are being generated)
Mitotic NEP cells
NEP cell end feet (clear space near ventricle)
telencephalic superventricle (future lateral ventricle)
Mitotic zone of pseudostratified NEP
137
138
PART PARTVI: VI: GW6.5 GW6.5 SAGITTAL SAGITTAL Carnegie Collection specimen #9247 (designated here as C9247) was collected in 1954 from a tubal pregnancy. The crown-rump length (CR) is 15 mm estimated to be at gestational week (GW) 6.5. C9247 was fixed in formalin, embedded in a celloidin/paraffin mix, and was cut in 8-µm sagittal sections that were stained with azan. Various orientations of the computer-aided 3-D reconstruction of M2051’s brain are used to show the gross external features of a GW6.5 brain (Figure 5). C9247’s sections are perfectly aligned in the sagittal plane. Considering all of the specimens in every volume of the Atlas, this is one of the best for quality of histological preservation and adherance to a section plane. Indeed, nearly an entire volume could be dedicated to the analysis of this brain. We photographed 64 sections at low magnification from the left to the right sides of the brain. Seven sections from the left side of the brain are illustrated in Plates 64AB to 70AB. Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (lowcontrast images) identify central neural structures. Plates 71AB to 84AB show high-magnification views of all parts of the developing brain. The sagittal plane is ideal to show the relative sizes of major brain subdivisions and the entry zones of sensory nerve fibers. The telencephalon is the smallest overall brain structure, composed mainly of a “stockbuilding” neuroepithelium surrounding an expanding telencephalic superventricle. The primordial plexiform layer adjacent to the cortical neuroepithelium has only scattered Cajal-Retzius cells. Migrating neurons are adjacent to the basal ganglionic and basal telencephalic neuroepithelia forming mounds in the floor of the telencephalon. The olfactory neuroepithelium is indistinct; a few pioneer olfactory nerve fibers get near the brain surface but do not appear to contact it. The diencephalon is the larger forebrain structure. The “stockbuilding” neuroepithelium surrounds a dorsally expanding superventricle in the future thalamic area. The neuroepithelium is shrinking in the hypothalamic and subthalamic areas where stem cells are depleted as they gener-
ate neurons. Migrating and settling young neurons accumulate in a thick band outside the neuroepithelium in the ventral diencephalic parenchyma adjacent to a thin subpial fibrous band. The mesencephalon is a prominent arch between the mesencephalic and diencephalic flexures. The roof (tectum and pretectum) of the mesencephalon contains a stockbuilding neuroepithelium adjacent to a very thin layer of pioneer migrating neurons. In comparison to the GW7 specimens, bundles of fibers in the posterior commissure are distinct but smaller. The tegmental and isthmal neuroepithelia are rapidly unloading their neuronal progeny in dense bands in the adjacent parenchyma. The outermost clumps of young neurons appear to interact with axons in the thick subpial fiber band. The rhombencephalon is the largest brain structure. Both the pons and medulla have neuroepithelia that are still relatively thick as stem cells unload their neuronal and glial progeny into an expanding parenchyma at a faster rate than the addition of new stem cells. The pons and medulla contain longitudinal bands of migrating cells, more dense just outside the neuroepithelium, less dense in the core, and again more dense adjacent to the subpial fiber band. The genu of the facial motor nerve forms fascicles adjacent to the neuroepithelium in both medial and lateral sections; these fascicles never reach the pial surface. What is presumed to be the solitary tract is the most prominent internal fiber tract in the medulla. Lateral sections show large peripheral sensory nerves contacting the brain. The mesencephalic nuclear neurons associated with the trigeminal nerve are migrating into the brain. The subpial fiber band is thicker where the axons from sensory ganglia enter the brain and appear to mingle with migrating neurons at the entry zones. As in the GW7 specimens, peripheral nerves have dense glia (Schwann cells), while central fiber tracts are clear. The cerebellum stands out as the most immature part of the rhombencephalon. All parts of the cerebellar neuroepithelium are stockbuilding neuronal and glial stem cells. Relatively indistinct layers are in the cerebellar transitional field.
139
EXTERNAL FEATURES OF THE GW6.5 BRAIN
4
Sub t h alamus ha lam us
m m ill a r bo d y
Ma
ot nd
ib
u
r
e
b
u l l
Upper rhombic lip
m
2
BRAINSTEM FLEXURES 1. Medullary 2. Pontine 3. Mesencephalic
Medullary velum
n
I n fu
C
e
4. Diencephalic
(with artifactual infoldings)
P
o
Preoptic area Optic evagination
s
yp
H
Basal telencephalon
3
m
al ga n g l i a
e
lu
as
A perfect sagittal cut through the brain is parallel to the midline in both horizontal and vertical directions. C9247 is a rare perfectly cut sagittal specimen.
Inferior colliculus
Isthmus
B
egment
m
c o r t
T
Superior colliculus
u
al
h a l a
ex
r e b C e r
T
Pretectum
mus ala u s ith m
Side view
Ep
y
Pineal evagination
A.
M e d
1
Front view
l
Lower rhombic lip
Spinal Spinal cord cord
Superior colliculus
B.
u
l a
Figure 5. A, The lateral view of the left side of a computer-aided 3-D reconstruction of the brain and upper cervical spinal cord in M2051, the preceding GW6.5 specimen, which has the same crown-rump length as C9247 (15 mm). External features are identified as in Figure 4B. The heavy numbered lines refer to brainstem flexures (boxed key). B, Front view of the brain in A. C, Back view of the brain in A.
C.
Superior colliculus
Back view
Pretectum
Inferior colliculus
Pineal evagination Epithalamus Isthmus
Vermis He
Pons Thalamus
Right side
Cerebellum
Left side Cerebral cortex
Medulla
Basal ganglia
Left side
m
isp
he
Cerebral cortex (occipital pole) re
Right side
Medullary velum
(with artifactual infoldings)
Pons
Rhombic lip border
Medulla
Spinal cord Spinal cord
Scale bars = 1 mm
PLATE 64A GW6.5 Sagittal, CR 15.0 mm C9247, Level 1: Slide 27 ll Section 14 sku and n ski Future dura?
enc
ephalic (future
su
aq
u
e t)
th al am ic
c
tr
Pia
p
ed
en
po ol
m
es
SID EO FB RA IN
u
(future lateral ventricle)
Pineal gland primordium
E FT
v
Ce
se
re
ENTIRE SECTION IS FR OM L
r
telencephalic superventricle
en ll- d
u f ut
e
Cell-sparse superarachnoid reticulum
(future third ventricle) Incipient telencephalic/ diencephalic choroid plexus
icl
diencephalic superventricle
dors al po ol
Basilar artery
hy su po bt th ha al la am m ic ic/ po ol
140
isthmal narrows canal
mammillary
foramen of monro Frontonasal process
ve nt ra lp oo l
recesses Pituitary (posterior lobe)
metencephalic pool
infundibular
rhombencephalic superventricle
Medial Medial nasal process
optic
Nasal septum
Sphenoid bone
Oral c av
Placodal Placodalepithelium epithelium
ity
Pituitary (anterior lobe)
Mandibular Mandibular arch arch (I)
o u e n g
Larynx
Sphenoid bone
T
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
(future fourth ventricle)
Maxillary process Maxillary
Epiglottis?
Ph yn x
Basal occipital bone Basilar artery
c ol u m n Body
myelencephalic pool
ar
Arytenoid swellings
Ve r t e b r a l
Medullary velum
Cell-sparse superarachnoid reticulum
Intervertebral disks Medullary velum
central canal
See the following for higher magnification views of this and nearby sections. Plates 72A and B: hippocampus and thalamus Plates 73A and B: hypothalamus Plates 74A and B: mesencephalic tegmentum Plates 76A and B: cerebellum
141
E
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold C
N N
E
IE D T h al am
ic m bic cortica lN E
Li
l plexiform la rdia o im Cingula te Pr
TELENCEPHALON
Mesencephalic (tegmental) NEP
Posterior complex
ing grat Mi
Dorsal complex
P
H
tegmental
Superior colliculus
ne
Mesencephalic (tectal) NEP
Isthmal neurons (sequestered in isthmal NEP?)
Inferior colliculus
Anterior complex Fornical GEP?
Nerve IV (trochlear)
Isthmal NEP
Posterior (mammillary)
Prefrontal
Hypothalamic NEP
Basal telencephalic NEP Septal NEP
Basal telencephalic neurons (sequestered in NEP?)
P
N
r ye
Pinealocyte GEP Epithalamic NEP
E
O
Brain surface (heavier line)
Pretectal NEP and posterior commissure GEP
s on ur
Hippocampal
P
ON
L
Migrating Cajal Retzius cells
AL
PLATE 64B C
A
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
PH
M E S E N
Cerebellar NEP (vermis) Migrating cerebellar deep nuclear neurons
Middle
Mi
g ra t aning b Pituicyte d s as ept al GEP a l te le ne nc u ro ep Preoptic ns hal ic NEP Migrating preoptic neurons Anterior Lamina terminalis Migrating anterior hypothalamic neurons
Pontine germinal zone
(predominantly midline raphe GEP)
R
Radially migrating cells
Upper rhombic lip
H
Pontomedullary trench
O N
Fibrous processes
Upper
C E
P
H
Midline raphe glial structure
(predominantly midline raphe GEP)
E
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Tangentially migrating cells
B
Labeled on this page: Central neural structures
Medullary germinal zones
M
Cell body layer
A
Radially migrating cells
L
O N
Fibrous processes
Ventr al fun iculus Ventral gray
Lower
Intermediate gray Dorsa l funic ulus
Ventral
Spinal NEP Dorsal gray
S P I N A L
C O R D
Intermediate Dorsal
Lower rhombic lip
Indentations in the mesencephalic tectum are artifacts of histological processing. The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricles as stockbuilding NEP cells decrease.
142
PLATE 65A GW6.5 Sagittal,CR 15.0 mm C9247, Level 2: Slide 25 Section 9 ll sku po ol th al am ic
c
t)
le )
icl
e isthmal narrows canal
l
dorsal pool
tr
Incipient telencephalic choroid plexus
telencephalic superventricle (future lateral ventricle)
foramen of monro
ventral pool
Cell-sparse superarachnoid reticulum
optic recess
Sphenoid bone
Maxillary Maxillary process Placodal Placodalepithelium epithelium
T
Or
Mandibular arch (I) Mandibular arch
u e n g
avity al c
o
ar x
m yel
yn
en ce
Medullary velum
phal
Basal occipital bone
ol ic po
Sympathetic chain ganglia?
Spinal nerves
Dorsal root ganglia
Ph
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Medullary velum
(future fourth ventricle)
Lateral nasal Lateral process
Na sal cav ity
metencephalic pool
rhombencephalic superventricle
Nerve I (olfactory) Frontonasal process Olfactory Olfactory epithelium epithelium Medial Medial nasal process Nostril
en
u
Pia
ed
(f su die ut p n ur e c hy su po bt e rv ep th e h th ha ir n a al la d tr li am m ve i c i c ic / nt cl po ri e o c
f
N AI
n se
nd na ski
v
-de
IS FR OM LEF TS ID EO F BR ephalic c n e s s u t (fu ure e p aq m e u r
ll Ce
Future dura?
re u tu
ENTIRE SECTION
Cell-sparse superarachnoid reticulum
See a higher magnification view of the hippocampus and thalamus from a nearby section in Plates 72A and B.
143
C
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
n M e s e c e p
N
Reticular complex
Hippocampal
N
Fornical GEP Anterior complex
ub
al
te r
Midd le?
t
An te rio r
P o n
e o p tic NEP
Pr
n
H
i
R
Reticular formation?
N e
Medial lemniscus?
Pontomedullary trench
E
Sprouting abducens (VI) and facial (VII) nerves?
N C
P
r
M
H
e
A
d
u O
N
Hypoglossal (XII) and vagal motor (X) nuclei?
Lower
Posterior intramural migratory stream (inferior olive neurons)?
Indentations in the mesencephalic tectum are artifacts of histological processing.
P N E
Prepositus nucleus?
r y l a
Raphe nuclear complex?
L
Reticular formation?
l
Migrating and settling medullary neurons
E
Raphe nuclear complex?
pe
Labeled on this page: Central neural structures
Raphe nuclear complex?
Up
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Upper rhombic lip
Migrating pontine neurons
B
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Cerebellar NEP (vermis)
M
Migrating hypothalamic neurons
Superficial fibrous layer
O
Brain surface (heavier line) Migrating olfactory neurons Migrating basal telencephalic neurons Migrating basal ganglionic and septal neurons Migrating preoptic neurons
Nerve IV (trochlear)
S
Hypothalamic NEP
Basal telencephalic NEP
Inferior collicular
Migrating subthalamic neurons
La
Insular? Olfactory cortical NEP
Mesencephalic (tectal) NEP
Migrating isthmal neurons
th
Septal and medial ganglionic NEP
A
Isthmal NEP
mic
Choroid plexus stem cells
P
ala
Limbic cortical NEP
E
ur
H
P
Retrosplenial?
i c ( t e g m a l tegmental n e h e ting gra Mi
P
E
N
c
E i
DI
T h a l a m
A
H al
tic
Dorsal complex
E
N
P
C
Superior collicular
N E P
Neocor
Epithalamic NEP
t a l )
T E L E N C E P
Posterior complex
n
N
E
E
s on
L
P
N
Pretectal NEP and posterior commissural GEP
O
Primordial plexiform layer
O
N
ON
PLATE 65B
L
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
E
AL
PH
M E S E
Gracile and cuneate nuclei?
Lower rhombic lip Ventral funiculus
Ventral gray La Intermediate te gray ra lf un icu l gray lu Dorsa s niculus Dorsal fu
S P I N A L
C O R D
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
144
ure
na ski
thalamic pool
m
es
e
halic ncep (future
su
aq
p
ed
e c
t)
(future third ventricle)
en
u
diencephalic superventricle
u
BR
v
Ce
e ll- d
ns
ut ef
IS FR OM LEF TS ID EO F
r
Future dura?
ENTIRE SECTION
N AI
PLATE 66A GW6.5 Sagittal, CR 15.0 mm C9247, Level 3: Slide 23 ll Section 8 sku nd
tr
icl
subthalamic pool
e
Pia
Incipient telencephalic choroid plexus dorsal pool Cell-sparse superarachnoid reticulum
telencephalic superventricle (future lateral ventricle)
ventral pool
Nerve I (olfactory) Frontonasal process Olfactory epithelium
metencephalic pool
Sphenoid bone
Nasal cavity
(future fourth ventricle)
Lateral nasal Lateral process
Carotid artery? Maxillary process Otic vesicle O
ra
lic ha ep nc le ye m
Plates 71A and B: neocortex Plates 75A and B: tectum, isthmus, and cerebellum
ty
g u e
avi l c
n
I) h( a rc la r ibu
o
nd
T
Ma
See the following for higher magnification views of this and nearby sections.
Arterial trunk
ol po
Petrous temporal bone Pharynx Inferior vagal ganglion (X)
rhombencephalic superventricle
optic recess
Medullary velum
Medullary velum
Basal occipital bone Cell-sparse superarachnoid reticulum
Sympathetic chain ganglia?
Nerve X (vagus)
Dorsal root ganglia
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
145
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
M
N
N
E
l a m i c a
DI
N EP
a
ic
rt
co
l a m i c a
A H
Raphe nuclear complex?
Migrating hypothalamic neurons
Migrating preoptic neurons
i
eb
e
ch ot
e (h
is m
ph
M
CTF1 (fibers)
e) er
l EP el eb rN er la c l l be ra te re La Ce
e
e
n ar
ch ot
Upper Dorsal rhombic lip
H
Medial lemniscus? Sprouting facial (VII) nerve?
O
Pontomedullary trench
M
B N
M d
u
Reticular formation
l l a
r y
we Lo
Vestibular nuclear complex?
r
N
Spinal nucleus V?
E
P
Solitary nucleus? Posterior intramural migratory stream (inferior olive neurons)?
O N A L P H C E
e
Migrating and settling medullary neurons
E
Reticular formation
r pe
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
t
er
rn
Up
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
n
n
di
c al
lla
R
Preoptic NEP Anterior hypothalamic NEP
E
N
P
P o
P
lay er
m
ifor
P
a l pl e x
h
Neo
T
T E L E N C E ri m o r d i
CTF2 (cells)
Migrating pontine neurons
Reticular formation?
Migrating basal ganglionic neurons
CTF3 (cells and fibers)
Migrating isthmal neurons
Medial forebrain bundle?
Migrating olfactory neurons Migrating basal telencephalic neurons
Inferior collicular
Isthmal NEP
Migrating subthalamic neurons Trochlear (IV) nucleus?
Bed nucleus of the stria terminalis
Brain surface (heavier line)
t
N
Substantia nigra? Oculomotor (III) nuclear complex? Interpeduncular nucleus?
t h
Globus pallidus?
(
P
Olfactory Basal cortical telenNEP cephalic NEP
A
N E
Insular?
l i c
a l ) c t
Sub
Strionuclear NEP
Medial ganglionic NEP
on s
H
O
Choroid plexus stem cells
Limbic cortical NEP
e p h a Superior
ig
P
c
collicular
Reticular complex
Fornical GEP?
E
cephalic (te e n egme gm n t al gt es neu M ratin r
Dorsal complex
Hippocampal
n
e
N
P Retrosplenial?
Posterior complex Epithalamic NEP
C
L
l
E
e
Pretectal NEP and posterior commissural GEP
EP l) N
N
E
P
M e
ta
L
E
ON
en
O
C
P
L HA
PLATE 66B
N
s
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
M E S E
Posterior commissure
Ventralrhombic Lower rhombiclip lip
Solitary tract?
Gracile and cuneate nuclei?
Labeled on this page: Central neural structures
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
146
PLATE 67A GW6.5 Sagittal, CR 15.0 mm C9247, Level 4: Slide 21 l Section 8 kul ds an
u
N AI
thalamic pool
e
u
ct
)
en
(future third ventricle)
tr
icle
subthalamic pool
Nerve III (oculomotor) Pia
v
diencephalic superventricle
d
ns
r
Future dura?
-de
kin es ur
IS FR OM LEF TS ID EO F p h BR e a c l n i c se su (futur me e p aq e
ll Ce
ut ef
ENTIRE SECTION
dorsal pool
telencephalic superventricle (future lateral ventricle)
Cell-sparse superarachnoid reticulum
ventral pool Nerve III (oculomotor) Nerve I (olfactory)
metencephalic pool
Olfactory Olfactory epithelium epithelium
rhombencephalic superventricle
Frontonasal process optic recess
(future fourth ventricle)
Lateral Lateral nasal process
Sphenoid bone
Nasal cavity Carotid artery?
Ciliary and otic ganglia? Otic vesicle
Maxillary Maxillary process
ye le nc ha
e ? g u
ep
vity al ca
c li po
ol
Inferior vagal ganglion (X)
n
Meckel's cartilage
Or
o
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
m
T
Mandibular Mandibular arch
Medullary velum
Petrous temporal bone
Medullary velum
Inferior glossopharyngeal ganglion (IX) Arterial trunk Basal occipital bone Cell-sparse superarachnoid reticulum Spinal nerves
Dorsal root ganglia
See the following for higher magnification views of this and nearby sections. Plates 74A and B: mesencephalic tegmentum Plates 81A and B: pons and upper medulla
147
CTF2 (cells)
r Ce
e
ia
lc
l be
e
la
rN
l
(h
EP
t La
er
a
ch
em
i
e lc
h sp
b re
e) er
e
lla
Up r pe
M
e
u
l
l
a r
Glossopharyngeal receptor neurons (IX)?
y
we Lo r
C
Vagal sensory neurons (X)?
ch
N
Upper Dorsal rhombic lip
M
d
Vestibular nuclear neurons (VIII)?
ot
O
alami c Th
EN
DI
Central auditory neurons (VIII)?
rn
H
M
ed
el
ot
C E P H A L O B E N
P e
b re
n ar
Pontomedullary trench
Facial motor (VII) neurons? Sprouting facial (VII) nerve? Facial sensory neurons (VII)?
Neurons migrating from the remnants of rhombomeric NEPS
t
i
n
P o
le x P N e o iform H c o lay r t er ic a
T E L E N C E P ri m o r di a l p
P
Reticular formation formation?
E
N
n
Medial lemniscus?
Anterior hypothalamic NEP Migrating hypothalamic neurons
CTF1 (fibers)
CTF3 (cells and fibers)
Medial forebrain bundle? Lateral Reticular hypoformation? formation thalamus
Migrating preoptic neurons Preoptic NEP
lem
Parabrachial nucleus?
Bed nucleus of the stria terminalis
Brain surface (heavier line) Migrating olfactory neurons Migrating basal telencephalic neurons Migrating basal ganglionic neurons
l
ra
te
La
? us
sc
ni
Migrating subthalamic neurons
NEP
Migrating isthmal neurons
Olfactory cortical Basal NEP? telencephalic NEP
The preoptic NEP, hypothalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Isthmal Inferior collicular NEP
Medial forebrain bundle?
Lateral ganglionic NEP
N
Red nucleus?
Strionuclear NEP
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
al) ct
Insular
NE
Subthalamic NEP
Limbic Hippocampal GEP? cortical (fornix) NEP
P
H nc A ep ha L li Superior c (t collicular e
Retrosplenial?
ic
E
e
P
S ub t h
EP
m a la
s
C
NE
N
Ventral complex
ncepha lic (teg se m (I M e lomotor II) nuclei e n ? ta u tegmen Oc rating t al ne ig ur M o
Epithalamic NEP
ns
l
N
Pretectal NEP and posterior commissural GEP
EP N Posterior complex
Central complex?
e
N
l)
A
L
O
E
A
M
O
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
PH
N LO
PLATE 67B
M E S E
N E
R
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Posterior commissure
P
Solitary tract? Ventralrhombic Lower rhombiclip lip Solitary nucleus Posterior intramural migratory stream (inferior olive neurons)? Solitary tract
Labeled on this page: Central neural structures
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
148
PLATE 68A GW6.5 Sagittal, CR 15.0 mm, C9247 Level 5: Slide 19, Section 8 Future
Pia
dura?
ll Ce
-de
ns
ef
u
ll sku nd na i k es tur
RAAIINN FBBR OOF DEE SIID
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
EENNTTIR IREESS EECCT TIO IONN ISISF FRRO OMM RLI EGFH TT m S su es (f pe en ut r c ur v ep e en h aq t a ue r li du ic c ct le ) diencephalic superventricle (future third ventricle)
dorsal pool
telencephalic superventricle
Cell-sparse superarachnoid reticulum
(future lateral ventricle)
ventral pool
Sphenoid bone
metencephalic pool
Carotid artery
Lateral nasal process
Facial (VII)? and vestibulocochlear (VIII) ganglia
Nerves VII and VIII boundary caps*
m ye le nc ep ha li c
Oral cavity
Otic vesicle
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
Mandibular arch (I)
rhombencephalic superventricle
Trigeminal ganglion (V)?
Nerve II (optic)
Maxillary process
(future fourth ventricle)
Frontonasal process
Meckel's cartilage
Medullary velum
po ol
Nerve IX
Petrous temporal bone
Arterial trunk
Vertebral artery?
Nerve X
Squamous occipital bone
Cell-sparse superarachnoid reticulum
Vagal (X) boundary cap* Superior vagal ganglion (X)
* Boundary caps are
Schwann cell GEPs?
149 FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Thal
CE DIEN
ating thala Migr m
Hippocampal? Posterior ganglionic/ amygdaloid NEP
Migrating subthalamic neurons
CTF3 (cells and fibers) CTF2 (cells)
Anterolateral ganglionic NEP
CTF1 (fibers) Lateral lemniscus?
Migrating amygdaloid neurons?
Reticular formation?
Migrating basal ganglionic neurons
N
P o n
Trigeminal (V) nuclear complex?
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Facial sensory neurons (VII)?
n
b (h ell e
i
re
t
P
Ce
GEP? (optic nerve)
e
E
Upper rhombic lip
Undulations in the NEP surface are remnants of the rhombomeres more prominent in less mature specimens.
Up r pe
Central auditory neurons (VIII)?
M e
d
ul la
Vestibular nuclear neurons (VIII)?
ry
Low er
NE
P
The tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
y ar lit t ac tr
Vagal sensory neurons (X)?
Neurons migrating from the remnants of rhombomeric NEPs
Lower rhombic lip
So
Glossopharyngeal receptor neurons (IX)?
R H O M B E N C E P H A L O N
pl e
Lateral lemniscus and brachium of inferior colliculus?
ce M re e d b ia no e lla l tc r h m ar is p N he E P re ) ce La re te b e ra l no lla tc r h
A
H P
N e xifor o c m la o y r
o r dial
N
N
T E L E N C E P ri m
A
li c
Inferior collicular
Migrating inferior collicular neurons?
Ventral complex
Brain surface (heavier line)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
a
tal) ec
Insular Olfactory cortical NEP?
ep ha lic (te l ne gm ur on s
h
H
O
ating tegme Migr nt a
Retrosplenial?
Limbic cortical NEP
Superior collicular
P
(t
a
P N E
Me
E
L
c er t i
l
P?
C
es en ce p
EP )N tal en
N
P
O
E
Labeled on this page: Central neural structures
Posterior Pre H complex P ns o r Epineu ic m i c N thalamic a NEP?
E al N tect
M
EP
A
N LO
M E S E N
nc se
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
L
PLATE 68B
Posterior commissure?
Solitary nucleus
Posterior intramural migratory stream (inferior olive neurons)?
Precerebellar NEP?
150
PLATE 69A GW6.5 Sagittal, CR 15.0 mm, C9247 Level 6: Slide 18, Section 8
ENTIRE SEC TIO NI SF RO M
Future dura?
ns
ef
u tu
S IN BRA OF
Ce
e ll- d
nd na ski e r
ll sku
LE FT
E ID
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
m su es (f pe en ut r c ur v ep e en h aq t a ue r li du ic c ct le )
dorsal pool
telencephalic superventricle (future lateral ventricle)
Cell-sparse superarachnoid reticulum
Pia
ventral pool
Sphenoid bone
Lateral nasal Lateral process
Nerves VII and VIII boundary caps*
Maxillary Maxillary process
m ye le nc ep ha li c
Facial (VII)? and vestibulocochlear (VIII) ganglia Mandibular arch (I) Mandibular arch
Oral cavity Nerve VIII Otic vesicle
Meckel's cartilage
Petrous temporal bone
X eI rv e N
po ol
Medullary velum
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal)
Superior vagal ganglion (X)
* Boundary caps are
rhombencephalic superventricle
Nerve II (optic)
metencephalic pool
Trigeminal ganglion (V) Nerve V
(future fourth ventricle)
Carotid artery
Frontonasal process
Trigeminal boundary cap*
Schwann cell GEPs? Vertebral artery?
Arterial trunk
Cell-sparse superarachnoid reticulum Squamous occipital bone
Vagal (X) boundary cap* Nerve X (vagal)
See the following for higher magnification views of this and nearby sections. Plates 76A and B: cerebellum Plates 77A and B: nerve V entry zone Plates 80A and B: nerves IX and X entry zones
151
PLATE 69B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
D I ENCE
Lateral lemniscus and brachium of inferior colliculus?
Hippocampal? Posterior ganglionic/ amygdaloid NEP
Brain surface (heavier line)
Anterolateral ganglionic NEP
CTF3 (cells and fibers) CTF2 (cells)
Reticular formation?
N
P
o
P
i n t
Undulations in the NEP surface are remnants of the rhombomeres more prominent in less mature specimens.
Trigeminal (V) nuclear complex?
M
r
ll ed u
pe
Facial sensory neurons (VII)? Central auditory neurons (VIII)?
Up
Lateral lemniscus?
Vestibular nuclear neurons (VIII)?
ry
a
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
E
e
Mesencephalic nucleus (V)
n
GEP? (optic nerve)
CTF1 (fibers)
Lateral lemniscus?
NE
P
Low er
Lower rhombic lip Precerebellar NEP?
Glossopharyngeal receptor neurons (IX)? Vagal sensory neurons (X)?
Neurons migrating from the remnants of rhombomeric NEPs
R H O M B E N C E P H A L O N
o
Migrating inferior collicular neurons?
Thalamic primordial plexiform layer
Retrosplenial?
M ed ia lc er C eb er no ell eb tc ar (h e h em lla is r N ph E La er P te e) ra lc er Up eb pe n el rr ho otc lar h m bi c lip
O
N e lay
L e xi
for
m
A a l pl
P ri m o r di
P
Migrating basal ganglionic neurons
The tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Inferior collicular
Migrating tegmental neurons? Mesencephalic (tegmental) NEP?
T
E N C E P E L H
Thalamic NEP (posterior complex)
Migrating amygdaloid neurons?
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
(
EP
Olfactory cortical NEP?
li c
N
Insular
Superior collicular
H
N
Limbic cortical NEP
a
P
O
o
NE
h
E
al) ct
c
al
ng t
C
te
er
r
c ti
r at i
c ne ami hal
ns u ro
Mese nc ep
L
Mig
Labeled on this page: Central neural structures N
P
HA
Migrating superior collicular neurons?
A
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
N LO
M E S E N
Solitary tract Solitary nucleus?
Posterior intramural migratory stream (inferior olive neurons)?
152
PLATE 70A GW6.5 Sagittal, CR 15.0 mm, C9247 Level 7: Slide 16, Section 8 Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Future dura?
LE FT
S
E ID
ll-
se den
f ut
u re
IN BRA OF
Ce
ENTIRE SEC TIO NI SF RO M
ll sku and n i sk
Cell-sparse superarachnoid reticulum
dorsal pool
telencephalic superventricle (future lateral ventricle)
ventral pool
Nerve V (opthalmic branch)
Pia Carotid artery
Trigeminal boundary cap* Trigeminal ganglion (V) Nerve V
EYE Pigment epithelium Intraretinal space Retinal NEP Vitreous body Sclera Pioneer retinal ganglion cells Eyelid
metencephalic pool
rhombencephalic superventricle
Medullary velum
(future fourth ventricle)
Fused Fused maxillary maxillaryprocess process and mandibular and mandibular archarch (I)
myelencephalic pool
Nerve Nerve V (maxillary V (maxillaryand and mandibularbranches) branches) mandibular
Vestibulocochlear (VIII) ganglion
Otic vesicle
HyoidHyoid arch arch (II)
Nerve V (trigeminal) Nerve VIII (vestibulocochlear)
Nerve VIII
Nerve VIII boundary cap*
ArchesIII IIIand and IV? IV? Arches Vertebral artery?
Arterial trunk
Petrous temporal bone
Cell-sparse superarachnoid reticulum
* Boundary caps are
Schwann cell GEPs?
us ? m o ne ua bo S q o ra l p tem
See the following for higher magnification views of nearby sections. Plates 78A and B: cerebellum, pons, and medulla Plates 79A and B: nerves V and VIII entry zones
153
PLATE 70B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
M E S E N
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
C
E
Migrating superior collicular neurons?
P
H
A
L O
N
Labeled on this page: Central neural structures Mesencephalic (superior collicular) NEP
Prim ord i
al pl e
x
rm ifo
l tica er lay c o r N
NEP Brain surface (heavier line)
eo
Limbic cortical (insular) NEP Corticoganglionic NEP?
Anterolateral ganglionic NEP
CTF1 (fibers) CTF2 (cells)
T
E L E N C
E
P
H
O N
L
A
CTF3 (cells and fibers)
Premigratory deep nuclear neurons and Purkinje cells sequestered in the cerebellar NEP NEP? ? Migrating Cajal-Retzius cells
The pontine NEP and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease. Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
EP
Peripheral VIII nerve (abundant glia)
A L O N
Medullary NEP
Vestibulo-auditory neurons Lateral lemniscus? (devoid of glia)
H
Undulations in the NEP surface are remnants of the rhombomeres more prominent in less mature specimens.
Vestibuloauditory neurons
Lower rhombic lip Cochlear NEP?
Migrating cochlear nuclear neurons?
O
Glial channels in Retinal NEP?
M B E N C E P
Peripheral nerve V (abundant glia)
P ontine N
The telencephalic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
Central trigeminal tract (devoid of glia)
H
Retinal NEP
re) he i sp m he Lateral P( cerebellar NE llar notch e reb e Upper C rhombic lip Medial cerebellar notch
Trigeminal nuclear complex
R
Migrating basal ganglionic neurons
GW6.5 Sagittal, CR 15.0 mm, C9247 Level 3: Slide 23, Section 8 See Level 3 in Plates 66A and B.
DORSAL NEOCORTEX
154
PLATE 71A
PLATE 71B Cell-dense future skin, skull, and dura Cell-sparse superarachnoid reticulum Brain surface (heavier line) Earliest settling Cajal-Retzius cells Migrating Cajal-Retzius cells
Blood islands outside pia Pia
Synthetic zone
Mitotic NEP cells predominate at ventricular border NEP - neuroepithelium The cortical NEP is in the "stockbuilding" phase when neural stem cells are increasing while few neurons (mainly Cajal-Retzius cells) are being generated.
telencephalic superventricle
Mitotic zone
NEP cell secretions empty into ventricle
Pseudostratified cortical NEP
Primordial plexiform layer
Terminal bars of NEP cells
(future lateral ventricle)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
155
GW6.5 Sagittal CR 15.0 mm C9247 Between Levels 1 and 2: Slide 26 Section 9 See Level 1 in Plates 64A and B; Level 2 in Plates 65A and B.
HIPPOCAMPUS AND THALAMUS
156
PLATE 72A
PLATE 72B
Pseudostratified thalamic NEP
Synthetic zone
Thalamic primordial plexiform layer
Terminal bars and secretory end feet of NEP cells
Cell-sparse superarachnoid reticulum
Cell-sparse future skull and skin
Mitotic zone
Migrating Cajal-Retzius cells
Future dura and dural blood vessels Blood islands near pia
Dorsal complex
Pioneer migrating thalamic neurons
Pia
at brain surface (heavier line)
Primordial plexiform layer Mitotic NEP cells
Synthetic zone Mitotic zone
Pseudostratified neocortical NEP
Thalamic NEP
Retrosplenial? Subicular?
Neocortical NEP Terminal bars and secretory end feet of NEP cells
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Primordial plexiform layer narrows over choroid plexus stem cells.
Ammon's horn Fornical GEP?
Limbic cortical NEP
telencephalic superventricle (future lateral ventricle)
"Budding" telencephalic choroic plexus Choroid plexus stem cells
Anterior complex
diencephalic superventricle
(future third ventricle)
The vascular bed of choroid plexus is continuous with superarachnoid reticulum.
157
GW6.5 Sagittal, CR 15.0 mm, C9247 Level 1: Slide 27, Section 14
A. Anterior hypothalamus and infundibular recess
B. Posterior hypothalamus and mammillary recess
HYPOTHALAMUS See Level 1 in Plates 64A and B.
158
PLATE 73A
PLATE 73B
A.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Preoptic NEP
floor of diencephalic superventricle
Anterior optic recess hypothalamic Anterobasal NEP
Optic chiasmal GEP?
nuclear NEP?
Middle hypothalamic NEP
infundibular recess
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
d an , ) g l lo b e y s is h ry ta rio r p o p i ti u ste hy P o ro ( p eu n
Migrating anterior hypothalamic neurons Pituitary gland (anterior lobe, adenohypophysis)
Arcuate nuclear NEP?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
ju n m ct es io en n M c be es en eph tw a ee ce ph lic n d su ie al pe nc ic rv ep te O g en ha c u m co l tr li o e m m nt ic c a pl o l n al ex to NE es d NE r (I P? II) P
Lamina terminalis
Pituicyte GEP
Rathke's pouch epithelium Rathke's pouch lumen
Interpeduncular nuclear NEP?
B. flo
or o f die nce
Posterior hypothalamic NEP (mammillary)
phal
ic su per
vent
ricle
mammillary recess
Middle hypothalamic NEP Brain surface (heavier line)
Migrating mammillary nuclear neurons?
Migrating tegmental neurons Migrating interpeduncular nuclear neurons?
159
160
PLATE 74A GW6.5 Sagittal CR 15.0 mm, C9247
MESENCEPHALIC TEGMENTUM
A.
Near Level 1: Slide 27 Section 7
B.
Level 4: Slide 21 Section 8
See level 1 in Plates 64A and B; level 4 in Plates 67A and B.
161
PLATE 74B
FONT KEY: Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - neuroepithelium
A.
c
p
t
M
e
P
Anterior
or
s Me
g tin tor u ro mo ? Sp ulo ons oc ax
2
Variously oriented layers of migrating tegmental neurons
en
presumed direction of axon growth in brain fiber tracts.
c tegmental NEP hali p ce
1
3
1
Oculomotor axons
Superarachnoid reticulum
Posterior
Oculomotor (III) neurons migrate only a short distance from NEP
ri
l
1. Predominantly radially radially-oriented oriented cells migrating parallel to the section plane. 2. Predominantly horizontally horizontallyoriented cells migrating perpendicular to the section Superficial layer plane. of predominantly horizontallylongitudinal fibers 3. Predominantly horizontally oriented cells migrating parallel to the section plane. Brain surface Arrows indicate the Arrows indicate the (heavier line)
B.
te
a
(future aqueduct)
Variously oriented layers of migrating tegmental neurons
presumed direction of neuron migration in the brain parenchyma.
An
lumen of the mesencephalic superventricle
E
2
s
e
1
t e g m e n
N
n
e
h
i c a l
Pioneer fibers of the medial longitudinal fasciculus?
Po
st
er
io
r
2
Oculomotor nerve roots
Superficial layer of predominantly longitudinal fibers Nerve III (oculomotor)
Deep layer of predominantly longitudinal fibers
162
PLATE 75A GW6.5 Sagittal CR 15.0 mm C9247 Near Level 3: Slide 24, Section 8 See Level 3 in Plates 66A and B.
MESENCEPHALIC TECTUM, ISTHMUS, AND CEREBELLUM
163
M
Migrating neurons surrounded by a fiber tract
PLATE 75B
Pi
on
e
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ee
s n
io r
c
co
eurons ular n ollic or c eri ( up i c gs tin a l ra h ig p rm e
e
r pe Su
ABBREVIATIONS: NEP - Neuroepithelium CTF - Cerebellar transitional field Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
l li c
EP rN ula
mesencephalic superventricle (future aqueduct)
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Cell-dense future skin, skull, and dura
t e c t a
l Pia with overlying blood islands
)
Inf e r i or c o lli c
Cell-sparse superarachnoid reticulum
N Pioneer migrating inferior collicular neurons (no surrounding fiber tract)
E
P NE ar ul
P Tr
oc
h
Is
le a rn
th m
Sprouting trochlear nerve fibers?
? u cl e a r N E P
al NEP
Trochlear (IV) nucleus?
Nerve IV (trochlear)
CTF1 (fibers) CTF2 (cells) CTF3 (cells and fibers)
Cerebellar NEP (hemisphere)
164
PLATE 76A
A.
B.
GW6.5 Sagittal, CR 15.0 mm, C9247 CEREBELLUM Level 1: Slide 27, Section 14 See Level 1 in Plate 64A and B.
Near Level 6: Slide 18, Section 5 See Level 6 in Plate 69A and B.
165
PLATE 76B
A.
Pioneer migrating inferior colliculus neurons
CTF1 (fibers) CTF2 (deep nuclear neurons)
Future fastigial nucleus?
Inferior collicular NEP
Nuclear transitory zone
Sprouting trochlear nerve fibers? Migrating trochlear nuclear neurons?
r NEP (verm a l l e is eb ) r e C
Isthma
Nerve IV (decussation, trochlear)
Mitotic NEP cells rhombencephalic superventricle
l
N
EP Spinocerebellar and vestibulocerebellar fibers?
CT CTF
(fibers)
2 (deep nucle
C T F 3 ( d e ep n u c l
Medial cerebellar notch
ere
bella
r
P E N
s
e ph
(h
e
re)
Lateral cerebellar notch Upper rhombic lip
rhombencephalic superventricle
ABBREVIATIONS: NEP - Neuroepithelium CTF - Cerebellar transitional field FONT KEY: Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Nuclear transitory zone
bers) and fi s n o eur ear n
Premigratory deep nuclear neurons and Purkinje cells sequestered in superficial cerebellar NEP?
C
ons) ar neur
i
Future dentate nucleus?
F1
Medullary velum
m
B.
Upper rhombic lip
Medullary velum Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
166
PLATE 77A
TRIGEMINAL NERVE ENTRY ZONE
GW6.5 Sagittal CR 15.0 mm C9247 Near Level 6: Slide 19, Section 3
See Level 5 in Plate 68A and B; Level 6 in Plate 69A and B.
167
PLATE 77B Pontine NEP (trigeminal NEP)
Mesencephalic nucleus (V)
Trigeminal nuclear complex (migrating and settling neurons)
Mesencephalic nucleus? Inward migrating neurons of the mesencephalic (V) nucleus
Penetrating trigeminal fibers
Ne
Penetrating trigeminal fibers
V
Nerve V
rve
Nerve V boundary cap
Nerve V
Trigeminal NEP
M igr
n P o
(source of all central trigeminal nuclei except mesencephalic)
a ti
t
ng
t ri
g
em
in
al
Me sen nuc ceph leu alic s?
Mesencephalic nucleus (V)
nu
cle ar
plex n
euro n s
Central trigeminal fibers penetrate brain
Mesencephalic nuclear neurons migrate into the brain from the periphery FONT KEY: Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Auditory-vestibular NEP d u ll a r er me p Up
P N E
i n e com
Nerve V boundary cap
y NE
P
Pioneer fibers of medial longitudinal fasciculus?
M igr
a ti n g c entral auditory neurons? t a L era Nucleus of the l l e m lateral lemniscus? Nucleus of the ni lateral lemniscus? sc us ?
Nerve V boundary cap (Schwann cell GEP?) Nerve V (trigeminal) Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Migrating vestibular neurons?
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
168
PLATE 78A
GW6.5 Sagittal, CR 15.0 mm, C9247 Near Level 7: Slide 16, Section 3 LATERAL CEREBELLUM, PONS, AND MEDULLA
See Level 7 in Plates 70A and B.
169
PLATE 78B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
CT
Arrows indicate the presumed direction of axon growth in nerves and fiber tracts.
P
atin re m cl lls, fir ) g i s g r P atory dee p nu TF4 (ce r C fi be F2 in je fie d s) i c t e p l l s ( ?) n c e C e T d F 3 l i ( d lum e l e p s n n , u u c f l e i a r r ct c s n ) t e w u n r a ons intermi l ed with ve of n? i s ti n g m d li o i C g r T a F t nto 1 a ng i i n ( f g i b rg ng e i d t r ee p ula s ega s ti b n s e gr u s c n l e o r a u r d ve e n d an l cor y af f e r e n t s f r o m s pin a
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
ABBREVIATIONS: NEP - Neuroepithelium CTF - Cerebellar transitional field
llar
ai ,m
r
metencephalic pool
NEP
(he
rhombencephalic superventricle
q u es
mis
(future fourth ventricle)
r ella re b
k ur
?) P? lls ce NE je kin ur (P F4 CT
Auditory-vestibular NEP Trigeminal NEP
Po at in
n ti
ig
gt rig
e mi
n al n
e Upp
ne NE P
r
Incoming trigeminal nerve fibers
Lower rhombic lip
Auditory (cochlear) NEP?
M
Pioneer fibers of the descending (spinal) trigeminal tract
myelencephalic pool
Undulations in the NEP surface are remnants of the rhombomeres more prominent in less mature specimens.
re)
ce the
phe
d) in t e re
Medial cerebellar notch
euro ns?
Central trigeminal tract with no interstitial glia
rm
M i g r at
Nerve V filled with Schwann cells
Nerve VIII filled with Schwann cells
Trigeminal ganglion (V)
n ar bul esti ing v
ry neurons? ito ? ud cus a l nis tr a em n l e c al M igrating te r s? f la cu Nucle u s o nis m e l al L ater
Nerve VIII boundary cap (Schwann cell GEP?)
Nerve V boundary cap (Schwann cell GEP?)
yN llar edu o
EP
?
ebe
st
and Purkinje c (se e l l s so j o u r n i n g rons neu wave of mig
Medullary velum
ns
Cer
e ar
nl
Nuclear transitory zones
Lateral Upper cerebellar rhombic lip notch
eu
r
Migrating cochlear nuclear neurons
No interstitial glia in central fiber tracts
Otic vesicle
Lumen
Epithelium Vestibulocochlear ganglion (VIII)
VIII ganglion neurons migrating from germinal source in otic epithelium?
See Level 7 in Plates 70A and B.
TRIGEMINAL AND VESTIBULOCOCHLEAR NERVE ENTRY ZONES
170
PLATE 79A GW6.5 Sagittal, CR 15.0 mm, C9247 Near Level 7: Slide 16, Section 13
PLATE 79B
rhombencephalic superventricle
M ig ra tin g
Pontin e an
ds
e tt l
in g
tri g e
Migrating vestibular neurons?
neuroepithelium (NEP)
n euro ns?
s? euron Migrating and settling auditory n
Spinal tract (V)?
at gr
in
g
lea nuc r lea ch o c
rn
on eur
s?
M i
Central trigeminal tract with no interstitial glia
m in al
Mitotic cells
Incoming trigeminal nerve fibers
Lateral lemniscus? (no interstitial glia)
Nerve V boundary cap (Schwann cell glioepithelium, GEP)
Incoming VIII nerve fibers
Nerve VIII boundary cap (Schwann cell GEP)
Nerve V (trigeminal) filled with Schwann cells filled with Schwann cells Nerve VIII (vestibulocochlear) filled with Schwann cells Arrows indicate the presumed direction of axon growth in nerves and fiber tracts.
Trigeminal ganglion (V)
Otic vesicle epithelium
Vestibulocochlear ganglion (VIII)
Arrows indicate the presumed direction of neuron migration from germinal sources. FONT KEY: Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
171
172
PLATE 80A GW6.5 Sagittal, CR 15.0 mm, C9247 Near Level 6: Slide 18, Section 13
A.
Nerve IX
B.
Nerve X
See Level 6 in Plates 69A and B.
ENTRY ZONES OF NERVES IX AND X
PLATE 80B
A.
Migrating vestibular nuclear neurons? Migrating central auditory neurons?
To solitary tract? To other tracts Bifurcating glossopharyngeal (IX) afferents Glossopharyngeal (IX) afferents penetrate brain.
Nucleus of the lateral lemniscus? Lateral lemniscus?
Interstitial glia absent in central fiber tracts
Nerve IX boundary cap (Schwann cell glioepithelium?) Nerve VIII Nerve VIII (vestibulocochlear)
Nerve IX (glossopharyngeal)
Peripheral blood vessels Vestibulocochlear (VIII) ganglion
Copious Schwann cell cords
B.
Migrating sensory vagal neurons? Solitary nucleus?
Solitary tract?
(glossopharyngeal [IX] and vagal [X] afferents)
Solitary
nucleus
?
Vagal axons join solitary tract?
Peripheral blood vessels
Nerve X Vagal (X) afferents penetrate brain at multiple sites
FONT KEY: Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the presumed direction of axon growth in nerves and fiber tracts.
Vagal axons disperse among migrating vagal sensory neurons and solitary nuclear neurons?
Copious Schwann cell cords Nerve X (vagus)
Copious Schwann cell cords
173
See Level 4 in Plates 67A and B.
MEDIAL PONS AND MEDULLA
174
PLATE 81A GW6.5 Sagittal, CR 15.0 mm, C9247 Level 4: Slide 21, Section 8
PLATE ?B 81B
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Mitotic cells near ventricular lumen
Pr
ed
Re
ti c
om
ul
ina
ar
ntly
P
reti cu la
rN EP ?
n
(future fourth ventricle)
t i n
A bd
u ce
e
Migra ting a EP bduc (V ens I ne ur
)?
s? on
Migrating reticular neurons?
m U p p e ro f r
Pontomedullary trench
E
ns nu cle ar N
N
e?
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - neuroepithelium
rhombencephalic superventricle
o
neur on s ojo ur nz on
Arrows indicate the presumed direction of neuron migration from germinal sources.
Fa
m h o
Vestibular nuclear complex neurons (VIII)?
P cia
lm
otor nuclear N
( EP
S ?
R e m n a n t s
V II
)?
Ventrolaterally migrating facial motor neurons?
Sprouting nerve VI (abducens)? Reticular formation?
y NE P lar l N E P u r i c ed bome
Facial sensory neurons (VII)?
Central auditory neurons (VIII)?
Sprouting VII nerve fibers segregate into bundles? Reticular formation?
Medial lemniscus intermingled with other unidentified fiber tracts?
Nerve VII facial genu
Lateral lemniscus?
neur ons in futur f uturee Settling neurons nuclei of the lateral lemnis cus?
175
GW6.5 Sagittal, CR 15.0 mm, C9247 Level 1: Slide 27, Section 14
A. ISTHMUS
B. UPPER PONS
See Level 1 in Plates 64A and B.
NEUROEPITHELIUM AND MIDLINE RAPHE GLIAL STRUCTURE
176
PLATE 82A
PLATE 82B
A.
isthmal canal
I
s
t
h
m
a
l
N
E
P
sthmal NEP?) in ist (sequestered s n o r u al ne I sth m
EP? ine raphe G l d i m ith led w g n hmal neurons and morphocyte t i s i g m n i r s? journ i n te a n d so g P n E i t N a l Isthma Migr he glial struc Cell body laye
ture morphocyt es
rap r of midline
des (thin relative to pons) Midline raphe glial fiber palisa Scattered cell bodies of another type of glia migrating among the fibrous palisades (less dense than Pons) pons)
B. Arrows indicate the presumed direction of cell migration from germinal sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Pontine floor plate
rhombencephalic superventricle
Cell body layer of midline raphe g lial structu re
morphoc yt e s
Midline raphe glia l fiber pali sades (thic k rel
ative to is thmus)
Scattered cell bodies of another type of glia migrating among the fibrous palisades (more dense than isthmus)
Dense clumps of migrating glia line up beneath morphocyte layer.
177
GW6.5 Sagittal, CR 15.0 mm, C9247 Level 1: Slide 27, Section 14 NEAR PONTINE FLEXURE
See Level 1 in Plates 64A and B.
NEUROEPITHELIUM AND MIDLINE RAPHE GLIAL STRUCTURE
178
PLATE 83A
PLATE 83B MORPHOCYTES are specialized glia that produce fibrous palisades in the region of the brain flexures and are the chief cell type in the midline raphe glial structure, first described in rats by Van Hartesveldt et al. (1986). See Volume 4, Plates 221A and B on pages 556-557 (Bayer and Altman, 2006). These fibers may provide structural stability as the brain curves during its rapid growth within the confines of the developing meninges, bone, and skin.
P Pontine NE
rhombencephalic superventricle
Mitotic cells
led with midline raphe GEP? g n i m r inte
w it ns or glia?) o r Tangentially mig u e n rating cells (
hin the midline raphe glial
s tru
cture
structure raphe glial e n i l d i m f ocytes) o C ell b o d y layer ( morph
lisades Thick midl ine raphe glial fiber pa Scattered cell bodies of another type of glia migrating among the fibrous palisades (note density increase posteriorly) FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the presumed direction of cell migration from germinal sources.
Dense clumps of radially migrating glia invade fibrous palisades.
179
GW6.5 Sagittal, CR 15.0 mm, C9247 Level 1: Slide 27, Section 14 MEDULLA (slightly anterior to medullary flexure)
See Level 1 in Plates 64A and B.
NEUROEPITHELIUM AND MIDLINE RAPHE GLIAL STRUCTURE
180
PLATE 84A
PLATE 84B End feet of NEP cells protrude into the floor of the rhombencephalic superventricle
Less dense deep NEP (tangentially cut in two places)
Med
NEP intermingled ullary
M it
with
midl
More dense superficial NEP
The morphocytes in the lower medulla differ in two ways from others. First, they are less densely packed. Second, the large cells migrating downward may be morphocytes themselves rather than the smaller cells migrating in the pons and isthmus (see Plates 82 and 83).
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ine
raph
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
zo n
e
e G EP ?
orphocytes) of midline raphe glia m ( r e y a l y l struc C e ll b o d ture d isper sed am on g
Thick midline raphe glial fiber pa lisade s
o tic
Syn
the
th e
tic
zo n
e
fib ers
Arrows indicate the presumed direction of cell migration from germinal sources.
181
182
PART PARTVII: VII: GW5.5 GW5.5 CORONAL CORONAL This specimen is embryo #1000 in the Minot Collection, designated here as M1000. The crown-rump length (CR) is 10 mm estimated to be at gestational week (GW) 5.5. Most of M1000’s forebrain and midbrain sections are cut (10 µm) in the coronal plane, but the plane shifts to predominantly horizontal in the posterior midbrain, pons, and medulla. We photographed 64 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and medulla. Fourteen of these sections are illustrated in Plates 85AB to 98AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of M1000’s brain and eye (Figure 6), and to show each illustrated section in situ (insets, Plates 85A to 98A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. Plates 99AB show high-magnification views of the telencephalic neuroepithelium. All parts of the telencephalic neuroepithelium are rapidly increasing their pool of neuronal and glial stem cells as they expand the shorelines of the enlarging telencephalic superventricle. However, the entire telencephalon is much smaller than in the GW6.5 specimens (Parts V and VI). The primordial plexiform layer adjacent to the cerebral cortical neuroepithelium is nearly devoid of cells except in far ventrolateral areas. The basal ganglionic and basal telencephalic neuroepithelia have only a thin layer of adjacent migrating neurons, many fewer than in the GW6.5 specimens. The posterior olfactory epithelium has only partially invaginated into a developing nasal cavity, while the anterior epithelium is a placode in the anterolateral head. Still, cellular densities outside the placode and invaginated epithelium may be supporting cells surrounding the first olfactory nerve fibers. The diencephalic neuroepithelium surrounds a superventricle that will narrow (shrinking shorelines) by GW6.5 in the preoptic, hypothalamic, and subthalamic areas. It is postulated that the superficial parts of the anterior hypothalamic and subthalamic neuroepithelia contain premigratory, postmitotic neurons that are sequestered there. More posteriorly, these neuroepithelia are surrounded by sequential waves of migrating neurons. In contrast, the thalamic neuroepithelium is in the “stockbuilding” stage, increas-
ing its population of neuronal and glial stem cells as the thalamic pool of the diencephalic superventricle expands. The eye is clearly connected to the ventral diencephalon by a thick, short stalk that is the glioepithelium of the future optic nerve. As in the more mature specimens, the retinal neuroepithelium is clearly differentiated from the pigment epithelium. The mesencephalon contains a stockbuilding neuroepithelium in the pretectum and tectum (virtually no adjacent migrating neurons). The tegmental and isthmal neuroepithelia are thick, but their population of stem cells begins to decrease as massive waves of migrating neurons leave. The subpial fiber band is considerably thinner than in the GW6.5 specimens. Both the pons and medulla have neuroepithelia that are thicker than at GW6.5, but are nevertheless shrinking as they unloaded their neuronal and glial progeny into an expanding parenchyma. In lateral areas, the neuroepithelium forms crescent-shaped evaginagions, the rhombomeres. The rhombomeres are associated with the entry zones of sensory cranial nerves V, VII, VIII, IX, and X; they will be the most distinctive features of the thombencephalon for the remainder of brain development. Cells are migrating and settling in longitudinal arrays at the pontine flexure. Most regions of the pons and medulla are characterized by large bands of migrating neurons with few nuclear divisions. A few cells are settling in the barely recognizable superior olivary complex and many are settling in the reticular formation throughout the pons and medulla. Some facial motor neurons are migrating from medial to lateral, leaving behind their axons in a small, but definite genu of the facial motor nerve. Migrating inferior olive neurons are in the posterior intramural migratory stream outside the precerebellar neuroepithelium in the posterior lower rhombic lip, but no neurons have settled in the inferior olivary complex. The solitary nucleus and tract cannot be identified, although solitary nuclear neurons are undoubtedly migrating outside the rhombomere 6 medullary neuroepithelium. The subpial fiber band is thick in the pons and medulla, especially at the entry points of the sensory nerves. The cerebellar neuroepithelium is much smaller than at GW6.5. Some early-generated deep nuclear neurons are migrating in the cellular layers of the cerebellar transitional field, but these and the fibrous layers are thinner and less definite than at GW6.5.
183
M1000 Computer-aided 3-D Brain Reconstructions B.
Angled front view
Pretectum
Side view am
u
T
s
Th
y p s o th al a m u
alamu
s o n
ce
Medullary velum
Rhombomere 2 Rhombomere 5
pe
m
r
BRAINSTEM FLEXURES
ulla
ed
er
w
we
rm
edu
1. Medullary lla
u ll
a
Lo
Lo
med
Upper rhombic lip
Up
p er
m ebellu Cer
P
a
ha i lona Su bth
Mammillary body
s
n
Inferior colliculus
2
Eye
s
Up
Eye
o
H
Infundibulum
n
P Preoptic area
3
Preoptic area
ph
g
Cereb
n gl S ia u bthal alo amu n s Hy po T thalam u s e
T
C
um
l co bra rt re
ll
u
n s a tele a l B B asa
4
th mu
be
Bas a l g a n g l Ba sal telen c e p
o
e
x
Is
re
m
s
P
corte
m tu
Ce
I s t h
Inferior colliculus
l ra
me e g
n
n t u m
s mu
l
al
la
x
Interhemispheric fissure
g m e
u s
e
m
Occipital pole
us am
ith Ep a
h a l a
Superior colliculus
Epit ha s l
s
Superior colliculus
P o n
Pretectum
s
A.
1
2. Pontine
m
ed
u l la
Lower rhombic lip
3. Mesencephalic Spinal cord
4. Diencephalic
Spinal cord
C.
Top view
Rhombomere 2
Occipital pole Eye
u
C e
p
s
l B a s a
Scale bars = 1 mm
g
a
n
Medullary velum Lower rhombic lip
a C o
m e d u
r
l
l
o
w
o
C
s
m e d u l l a
p
o
us m a t l h a T m e g m e n t u
al
li a
ph
g
Basal telence
H
n
y
Preoptic area
S
Interhemispheric fissure
Isthmus
Rhombomere 2 Rhombomere 5
Eye
ex
e p t u m
rt
C
Frontal pole
erebral c o
Bottom view
n
e r
D.
o
re
P
e
o r t e x
e r p p
C
U
l
P o n s
a
n s P o
r
be
e
P
E
r b
S u p e r i o r c o l l i c u l u s
i n a l
m
Ve r m i s
a
llu m
l
u i t h a l a m
a
L
T h
d
Interhemispheric fissure
r e t e c t u m
s
ere isph H em
Frontal pole
Figure 6. A, The left side of the 3-D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
S
p
184
PLATE 85A GW5.5 Coronal CR 10 mm M1000 Level 1: Section 29
Non-neural structures labeled Interhemispheric fissure
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Level 1: Computer-aided 3-D Brain Reconstruction Pia
Olfactory placode Hypothetical olfactory induction field
185
PLATE 85B
Neural structures labeled
TELENCEPHALON CEREBRAL CORTEX
Dorsal limbic cortical NEP?
Brain surface (heavier line)
Neocortical NEP? anterior pool
telencephalic superventricle
(future lateral ventricle)
Cell sparse cortical primordial plexiform layer (neurons have not yet migrated from NEP)
Ventral limbic cortical NEP? Telencephalic roof plate
(stem cells of telencephalic choroid plexus?)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Primordial plexiform layer absent in roof plate
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
186
PLATE 86A GW5.5 Coronal CR 10 mm M1000 Level 2: Section 42
Peripheral neural and non-neural structures labeled Interhemispheric fissure
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
See a high magnification view of the telencephalon in a nearby section in Plates 99A and B.
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Level 2: Computer-aided 3-D Brain Reconstruction
Pia
Nerve I (olfactory)? Olfactory placode
Hypothetical olfactory induction field
187
PLATE 86B
Central neural structures labeled Telencephalic/diencephalic roof plate (stem cells of choroid plexus?)
TELENCEPHALON
Primordial plexiform layer absent in roof plate
CEREBRAL CORTEX
Brain surface (heavier line)
Dorsomedial limbic cortical NEP?
dorsal pool
Neocortical NEP?
telencephalic superventricle (future lateral ventricle)
Cell sparse cortical primordial plexiform layer (neurons have not yet migrated from NEP)
future roof of third ventricle
foramen of monro
Ventrolateral limbic cortical NEP? Olfactory cortical NEP?
ventral pool
Basal telencephalic NEP
BASAL GANGLIA/ BASAL TELENCEPHALON
Septal NEP Pioneer migrating septal and basal telencephalic neurons* Telencephalic floor plate
*Note that the group of basal telencephalic migrating neurons may contain mitral cells heading for the future olfactory evagination.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
188
PLATE 87A GW5.5 Coronal CR 10 mm M1000 Level 3: Section 100
Peripheral neural and non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Pia
See a high magnification view of the telencephalon in a nearby section in Plates 99A and B. Naso-optic furrow Nerve I (olfactory)?
Hypothetical olfactory induction field Nostril opening to olfactory invagination and nasal cavity Lateral nasal process Medial nasal process Nasal septum/roof of oral cavity
Placodal epithelium Olfactory epithelium
Level 3: Computer-aided 3-D Brain Reconstruction
The GW5.5 Face and Neck
Figure 247C modified (Patten, 1953, p. 429.)
Nasal septum Medial nasal process
Frontal prominence
Naso-optic furrow Eye Lateral nasal process Nostril Mouth Mandible Hyo-mandibular cleft
Maxillary process Mandibular arch (I) Hyoid arch (II) Laryngeal cartilages?
189
PLATE 87B Central neural structures labeled DIENCEPHALON
Diencephalic roof plate
THALAMUS
(primordium of choroid plexus?) Dorsal complex?
Thalamic NEP
Primordial plexiform layer thinner in roof plate Thalamic primordial plexiform layer
Reticular nuclear
(future third ventricle)
TELENCEPHALON
diencephalic superventricle
CEREBRAL CORTEX Dorsomedial limbic cortical NEP?
Neocortical NEP? dorsal pool
Ventrolateral limbic cortical NEP?
Primordial plexiform layer thinner in roof plate Telencephalic roof plate
(primordium of choroid plexus?)
Brain surface (heavier line) Cortical primordial plexiform layer
telencephalic superventricle
(future lateral ventricle)
Olfactory cortical NEP?
foramen of monro
Corticoganglionic NEP Anterolateral ganglionic NEP
ventral pool
Pioneer migrating basal gangliionic neurons
Basal telencephalic NEP
BASAL GANGLIA/ BASAL TELENCEPHALON
Septal NEP? Pioneer migrating septal and basal telencephalic neurons* Telencephalic/diencephalic floor plate
(lamina terminalis in junction of preoptic area and septum?)
*Note that the group of basal telencephalic migrating neurons may contain mitral cells heading for the future olfactory evagination.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
190
PLATE 88A GW5.5 Coronal CR 10 mm M1000 Level 4: Section 128
Peripheral neural and non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Dural blood vessels
See a high magnification view of the telencephalon and diencephalon in a nearby section in Plates 99A and B. Level 4: Computer-aided 3-D Brain Reconstruction
Pia
Naso-optic furrow Eye covering Olfactory epithelium Maxillary process
Nerve I (olfactory)? Nasal cavity
Placodal epithelium Medial nasal process
Nasal septum/roof of oral cavity Hypothetical olfactory induction field
191
PLATE 88B
Central neural structures labeled
DIENCEPHALON EPITHALAMUS
Diencephalic roof plate
(primordium of pineal gland)
Epithalamic NEP
pineal recess
THALAMUS
Posterior complex?
Brain surface (heavier line)
Dorsal complex?
Thalamic NEP
Thalamic primordial plexiform layer
Ventral complex?
thalamic pool
Premigratory thalamic neurons sequestered in thalamic NEP?
Reticular nuclear Anterior complex
diencephalic superventricle (future third ventricle)
TELENCEPHALON CEREBRAL CORTEX
subthalamic pool
Neocortical and limbic cortical NEP posterior pool
Corticoganglionic NEP
telencephalic superventricle (future lateral ventricle) foramen of monro
Sequestered and pioneer migrating reticular nuclear neurons? Sequstered and pioneer migrating anterior thalamic neurons? Cortical primordial plexiform layer Premigratory Cajal-Retzius cells and subplate neurons sequestered in cortical NEP?
Posterior ganglionic NEP
BASAL GANGLIA/ AMYGDALA
Amygdaloid NEP? Strionuclear NEP?
preoptic pool
Sequestered and migrating amygdaloid neurons?
Lateral area?
PREOPTIC AREA
Preoptic NEP
Sequestered and migrating posterior basal ganglia neurons?
Sequestered and migrating lateral preoptic area neurons?
Medial area?
Sequestered and migrating medial preoptic area neurons?
DIENCEPHALON
Diencephalic floor plate
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
192
PLATE 89A GW5.5 Coronal CR 10 mm M1000 Level 5: Section 169
Peripheral neural and non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Dural blood vessels Pia and pial blood vessels Naso-optic furrow
Orbitosphenoid process? Oral cavity
Maxillary process Palatal process Mandibular arch (I)
Nerve II (optic) Pigment epithelium Intraretinal space Retinal NEP Vitreous body Lens Sclera/cornea
Tongue
Eye
Level 5: Computer-aided 3-D Brain Reconstruction
Hyo-mandibular cleft Meckel's cartilage in mandibular arch (I)
193
PLATE 89B
Central neural structures labeled MESENCEPHALON PRETECTUM?
Mesencephalic roof plate
(posterior commissural GEP?)
Pretectal NEP? Pretectal primordial plexiform layer mesencephalic superventricle
DIENCEPHALON THALAMUS
(future aqueduct)
Posterior complex (dosal lateral geniculate)?
Brain surface (heavier line) Thalamic primordial plexiform layer
Ventral complex?
Thalamic NEP
Posterior complex (medial geniculate)?
thalamic pool
Reticular nuclear
diencephalic superventricle (future third ventricle)
SUBTHALAMUS
Subthalamic NEP
subthalamic pool
Retinal NEP
Sequstered and pioneer migrating subthalamic neurons?
Sequestered and pioneer migrating lateral preoptic area neurons?
Lateral area NEP? Medial area NEP?
Sequestered and pioneer migrating reticular nuclear neurons? Subthalamic primordial plexiform layer
PREOPTIC AREA
Preoptic and optic germinal zones
Premigratory thalamic neurons sequestered in thalamic NEP?
preoptic/hypothalamic pool optic recess
Optic nerve (II) and tract GEP?
HYPOTHALAMUS Migrating anterobasal nuclear neurons?
Anterior hypothalamic NEP?
Glial channels for optic chiasm and tract?
Diencephalic floor plate
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
194
PLATE 90A GW5.5 Coronal CR 10 mm M1000 Level 6: Section 192
Peripheral neural and non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case) and blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Pia and pial blood vessels Internal carotid artery
Orbito-sphenoid process?
Naso-optic furrow
Maxillary process Oral cavity Mandibular arch (I)
Hyo-mandibular cleft Pigment epithelium Intraretinal space
Tongue
Retinal NEP Sclera
Eye
Hyoid arch (II) Meckel's cartilage? in mandibular arch Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule) Rathke's pouch (primordium of adenohypophysis)
Level 6: Computer-aided 3-D Brain Reconstruction
195
PLATE 90B
Central neural structures labeled MESENCEPHALON PRETECTUM?
Mesencephalic roof plate (posterior commissural GEP?)
Posterior commissure (pioneer fibers)
Pretectal NEP? mesencephalic superventricle
DIENCEPHALON THALAMUS
Brain surface (heavier line)
Posterior complex (dosal lateral geniculate)? Ventral complex?
Thalamic NEP
Pretectal primordial plexiform layer
(future aqueduct)
Thalamic primordial plexiform layer thalamic pool
Posterior complex (medial geniculate)? Reticular nuclear
diencephalic superventricle
Sequestered and pioneer migrating reticular nuclear neurons
(future third ventricle)
SUBTHALAMUS
Subthalamic primordial plexiform layer
Subthalamic NEP?
subthalamic pool
HYPOTHALAMUS
Hypothalamic NEP
Premigratory thalamic neurons sequestered in thalamic NEP?
Sequential waves of migrating subthalamic neurons
Sequential waves of migrating lateral hypothalamic area neurons?
Lateral area NEP? hypothalamic pool
Medial forebrain bundle?
Anterior NEP?
Migrating anterior hypothalamic neurons
infundibular recess
Diencephalic floor plate (median eminence?)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
196
PLATE 91A GW5.5 Coronal CR 10 mm M1000 Level 7: Section 215
Peripheral neural and non-neural structures labeled
Cell-dense primordial mesenchymal brain case (skin/bone)
Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Future dura (internal border of brain case) and blood vessels
Middle cerebral artery?
Ali-sphenoid process? Anterior cardinal vein
Meckel's cartilage?
P
Fused maxillary process and mandibular arch arch(I)
e
al b por tem s ou tr
o ne
Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule) Primordia of sphenoid and basal occipital bones
Level 7: Computer-aided 3-D Brain Reconstruction
Trigeminal ganglion (V) Rathke's pouch (primordium of adenohypophysis)
Otic placode
Nerve V (trigeminal)
197
PLATE 91B
Central neural structures labeled MESENCEPHALON PRETECTUM/SUPERIOR COLLICULUS?
Mesencephalic roof plate (posterior commissural GEP?)
Posterior commissure (pioneer fibers) Pretectal primordial plexiform layer
Pretectal?
Brain surface (heavier line)
Tectal NEP Superior collicular?
mesencephalic superventricle (future aqueduct)
Superior collicular primordial plexiform layer
TEGMENTUM
Tegmental NEP
Migrating mesencephalic tegmental neurons
(reticular formation, red nucleus, oculomotor (III) complex?)
SUBTHALAMUS
diencephalic superventricle
(future thirdventricle)
subthalamic pool
Subthalamic NEP?
HYPOTHALAMUS Lateral area?
Hypothalamic NEP
Middle?
hypothalamic pool
Arcuate?
Subthalamic primordial plexiform layer Sequential waves of migrating subthalamic neurons
Sequential waves of migrating lateral hypothalamic area neurons? Migrating middle hypothalamic neurons Medial forebrain bundle?
DIENCEPHALON infundibular recess
Diencephalic floor plate
(median eminence and pituicyte GEP of the neurohypophysis?)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
198
PLATE 92A GW5.5 Coronal CR 10 mm M1000 Level 8: Section 237
Peripheral neural and non-neural structures labeled
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Pia and pial blood vessels Future dura (internal border of brain case) and blood vessels
Circle of Willis artery? Middle cerebral artery?
Cell-dense primordial mesenchymal brain case (skin/bone)
Ali-sphenoid process?
Vestibular ganglion (VIII)?
ior c ardinal vein
Trigeminal ganglion (V)
Nerve V (trigeminal)
Petrous temporal bone
An
ter
Facial ganglion (VII)?
B a s i l a r
Budding spiral ganglion (VIII)?
a r t e r y
Sella turcica?
Basal occipital bone?
Inferior vagal ganglion (X)? Inferior glossopharyngeal ganglion (IX)? Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule)
Level 8: Computer-aided 3-D Brain Reconstruction
199
PLATE 92B Central neural structures labeled MESENCEPHALON
Mesencephalic roof plate (commissural GEP?)
TECTUM
Commissure of the superior colliculus? (pioneer fibers)
Superior collicular NEP
Brain surface (heavier line) mesencephalic superventricle (future aqueduct)
Superior collicular primordial plexiform layer
TEGMENTUM
Tegmental NEP
Successive waves of migrating mesencephalic tegmental neurons
diencephalic superventricle
(future third ventricle, mammillary recess)
Pioneer migrating mammillary neurons
Hypothalamic NEP
(posterior, mammillary)
Hypothalamic NEP
(middle)
HYPOTHALAMUS
DIENCEPHALON
Medial forebrain bundle? Pioneer migrating middle hypothalamic neurons
infundibular recess
Diencephalic floor plate
(pituicyte GEP in neurohypophysis?)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
200
PLATE 93A
Peripheral neural and non-neural structures labeled
GW5.5 Coronal CR 10 mm M1000 Level 9: Section 255
Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Circle of Willis artery (posterior cerebral)?
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case) and blood vessels
Basilar artery
Nerve V boundary cap Nerve V (trigeminal) Trigeminal ganglion (V)
Nerve VIII boundary cap Nerve VIII (vestibulocochlear) Facial ganglion (VII)
Schwann cell GEP in boundary caps? Vestibular ganglion (VIII)
Petrous temporal bone
Inferior glossopharyngeal ganglion (IX)?
Inferior vagal ganglion (X)?
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule) Anterior cardinal vein
Level 9: Computer-aided 3-D Brain Reconstruction
201 Central neural structures labeled
PLATE 93B
Mesencephalic roof plate
(commissural GEP?)
MESENCEPHALON
Brain surface (heavier line)
TECTUM
Superior collicular NEP
Superior collicular primordial plexiform layer
mesencephalic superventricle (future aqueduct)
Successive waves of migrating mesencephalic tegmental neurons
TEGMENTUM
Tegmental NEP
Medial forebrain bundle?
DIENCEPHALON
(posterior tip of mammillary body)
Midline raphe glial structure Medial lemniscus?
PONS
Pontine floor plate
(midline raphe glial structure GEP)
Longitudinal domains of migrating and settling pontine neurons Trigeminal nuclear complex
rhombencephalic superventricle
(future fourth ventricle)
Medial pontine NEP Pontine floor plate
Pontine reticular formation
Central trigeminal tract Migrating raphe nuclear complex neurons?
(midline raphe glial structure GEP)
Lateral lemniscus?
RHOMBENCEPHALON
Medial lemniscus? Medial longitudinal fasciculus? Midline raphe glial structure
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
202
PLATE 94A
Peripheral neural and non-neural structures labeled
GW5.5 Coronal CR 10 mm M1000 Level 10: Section 269 Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone) Basilar artery Future dura (internal border of brain case) and blood vessels
Nerve V boundary cap Schwann cell GEP in boundary caps? Nerve VIII boundary cap Nerve VIII (vestibulocochlear) Vestibular ganglion (VIII)
Petrous temporal bone
Superior glossopharyngeal ganglion (IX)? Superior vagal ganglion (X)?
Vertebral artery Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule)
Level 10: Computer-aided 3-D Brain Reconstruction
203 Central neural structures labeled MESENCEPHALON
PLATE 94B
Mesencephalic roof plate (commissural GEP?)
TECTUM Superior collicular NEP
Brain surface (heavier line) Premigratory superior collicular neurons sequestered in the superior collicular NEP?
mesencephalic superventricle
Superior collicular primordial plexiform layer
(future aqueduct)
TEGMENTUM Medial forebrain bundle?
Tegmental NEP
Successive waves of migrating mesencephalic tegmental neurons
Midline raphe glial structure
PONS
Medial lemniscus?
Pontine floor plate
(midline raphe glial structure GEP)
Trigeminal motor nucleus (V)? Trigeminal sensory nuclear complex (V)
Medial pontine NEP
Central trigeminal tract
Pontine reticular formation
Sequential waves of migrating pontine neurons Premigratory facial motor nuclear (VII) neurons intermingled with abducens (VI) nuclear neurons?
rhombencephalic superventricle
(future fourth ventricle)
Medial medullary NEP
Posterior extension of trigeminal nuclear complex?
Medullary reticular formation
Nerve VII genu (facial) interspersed with migrating facial motor neurons? Migrating raphe nuclear complex neurons?
Medullary floor plate
(midline raphe glial structure GEP)
Lateral lemniscus?
MEDULLA
RHOMBENCEPHALON
Superior olivary complex neurons? Medial lemniscus?
Medial longitudinal fasciculus?
Midline raphe glial structure Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
204
Peripheral neural and non-neural structures labeled
PLATE 95A GW5.5 Coronal CR 10 mm M1000 Level 11: Section 285 Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone) Nerve III sheath (oculomotor)
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case) and blood vessels
Nerve VIII boundary cap (Schwann cell GEP?) Spiral ganglion (VIII) budding from otic epithelium?
Level 11: Computer-aided 3-D Brain Reconstruction
Superior glossopharyngeal ganglion (IX)?
Petrous temporal bone
Superior vagal ganglion (X)?
Dorsal root ganglion
Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule)
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
205
Central neural structures labeled
Mesencephalic roof plate
(commissural GEP?) Brain surface (heavier line)
MESENCEPHALON TECTUM
Superior collicular NEP
PLATE 95B
Superior collicular primordial plexiform layer
mesencephalic superventricle (future aqueduct)
TEGMENTUM
Tegmental NEP PROPOSED RHOMBOMERE IDENTITIES
Medial forebrain bundle? R2 Successive waves of migrating mesencephalic tegmental neurons
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
R3 R4
PONS
Midline raphe glial structure Medial lemniscus?
R5
Pontine floor plate
(midline raphe glial structure GEP)
Medial pontine NEP Pontine reticular formation
R2
(trigeminal NEP)
Trigeminal sensory nuclear complex (V) Central trigeminal tract Migrating trigeminal neurons?
rhombencephalic superventricle
Trigeminal sensory nuclear complex (V)
(future fourth ventricle)
R3
Migrating sensory neurons that will receive input from the facial ganglion (VII)?
(facial sensory NEP?)
Lateral pontine NEP
R4
Migrating auditory and vestibular neurons?
R5
Lateral lemniscus?
Lateral medullary NEP
Nucleus of the lateral lemniscus?
Medullary reticular formation
Medial medullary NEP
Migrating raphe nuclear complex neurons? Posterior intramural migratory stream (inferior olive neurons)?
Medullary floor plate
(midline raphe glial structure GEP)
Medial lemniscus?
MEDULLA
RHOMBENCEPHALON
Midline raphe glial structure
SPINAL CORD ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Medial longitudinal fasciculus?
Spinal floor plate
Spinal germinal zones
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
(midline raphe glial structure GEP)
Ventral funiculus Ventral gray
Ventral NEP
Intermediate NEP
Intermediate gray central canal
Dorsal NEP Spinal roof plate
Lateral funiculus Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
206
PLATE 96A GW5.5 Coronal CR 10 mm M1000 Level 12: Section 308
Peripheral neural and non-neural structures labeled Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case) and blood vessels
Nerve VIII boundary cap (Schwann cell GEP?) Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule)
Medullary velum
Level 12: Computer-aided 3-D Brain Reconstruction
Petrous temporal bone
NerveX boundary cap (Schwann cell GEP?) Superior vagal ganglion (X)?
Nerve X (vagis) Nerve XI (spinal accessory)
Dorsal root boundary cap (Schwann cell GEP?)
Cell-sparse superarachnoid reticulum (parenchymal expansion zone)
207
Central neural structures labeled
Mesencephalic roof plate
MESENCEPHALON
(commissural GEP?)
Brain surface (heavier line) Superior collicular primordial plexiform layer
TECTUM
Superior collicular NEP
PROPOSED RHOMBOMERE IDENTITIES
mesencephalic superventricle
R4
(future aqueduct)
TEGMENTUM
Tegmental NEP
Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
R5
Migrating mesencephalic tegmental neurons Mesencephalic reticular formation
Isthmal NEP
R6
isthmal canal
ISTHMUS
PLATE 96B
Migrating isthmal neurons
CTF1 (fibers) CTF2 (deep neurons) CTF3 (fibers)
CEREBELLUM
Cerebellar NEP PONS
CTF4 (cells)
metencephalic pool
Medial cerebellar notch
Lateral pontine NEP
Premigratory deep neurons and Purkinje cells sequestered in the superficial cerebellar NEP?
R2
Metencephalic roof plate
rhombencephalic superventricle
(upper rhombic lip)
(future fourth ventricle)
Auditory (cochlear) NEP?
Layers of the cerebellar transitional field (CTF)
Myelencephalic roof plate (lower rhombic lip)
R4
Lateral medullary NEP
Migrating cochlear nuclear neurons?
R5
Migrating auditory and vestibular neurons?
myelencephalic pool
R6 Migrating solitary nuclear neurons? (glossopharyngeal receptors)
Medial medullary NEP
(reticular formation, raphe complex, prepositus, vagal motor [X], and hypoglossal [XII])
Medullary reticular formation
Posterior intramural migratory stream (inferior olive neurons)? Spinocerebellar tracts? Migrating raphe nuclear complex neurons?
MEDULLA Medullary/ spinal reticular formation
RHOMBENCEPHALON SPINAL CORD Ventral? (merging with
medial medullary NEP)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Ventral gray?
Spinal NEP
Intermediate gray Intermediate
central canal
Dorsal Spinal roof plate
Lateral funiculus Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
208
Peripheral neural and non-neural structures labeled
PLATE 97A GW5.5 Coronal CR 10 mm M1000 Level 13: Section 334
Pia and pial blood vessels
Cell-sparse superarachnoid reticulum (brain parenchymal expansion zone)
Cell-dense primordial mesenchymal brain case (skin/bone)
Future dura (internal border of brain case) and blood vessels
Otic vesicle and epithelium (future cochlea, semicircular canals, utricle, and saccule)
Medullary velum
Level 13: Computer-aided 3-D Brain Reconstruction
Petrous temporal bone
Cell-sparse superarachnoid reticulum (parenchymal expansion zone)
209
Central neural structures labeled
PLATE 97B
MESENCEPHALON
Mesencephalic roof plate (commissural GEP?) Brain surface (heavier line)
TECTUM
Superior collicular NEP
PROPOSED RHOMBOMERE IDENTITIES
Superior collicular primordial plexiform layer
R5 mesencephalic superventricle
Inferior collicular NEP
(future aqueduct)
R6
Inferior collicular primordial plexiform layer R7
ISTHMUS
Isthmal NEP
Successive waves of migrating isthmal neurons?
isthmal canal
CEREBELLUM
Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Layers of the cerebellar transitional field (CTF) CTF1 (fibers) CTF2 (deep neurons)
Cerebellar NEP
Medial cerebellar notch
metencephalic pool
rhombencephalic superventricle (future fourth ventricle)
MEDULLA
myelencephalic pool
R5?
Lateral medullary NEP
CTF3 (fibers) CTF4-5? (deep neurons) Premigratory deep neurons and Purkinje cells sequestered in the superficial cerebellar NEP?
Metencephalic roof plate (upper rhombic lip)
Myelencephalic roof plate (lower rhombic lip)
R6
R7
Migrating glossopharyngeal receptor neurons? Migrating vagal sensory (X) neurons? Spinocerebellar tracts?
Lower medullary NEP
(gracile and cuneate NEPS merge with dorsal spinal NEP)
Migrating gracile and cuneate nuclear neurons?
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Lower medullary roof plate
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
210
PLATE 98A GW5.5 Coronal CR 10 mm M1000 Level 14: Section 376
Peripheral neural and non-neural structures labeled Pia and pial blood vessels
Cell-dense primordial mesenchymal brain case (skin/bone)
Cell-sparse superarachnoid reticulum (parenchymal expansion zone)
Future dura (internal border of brain case) and blood vessels
Medullary velum
Level 14: Computer-aided 3-D Brain Reconstruction
211
PLATE 98B
Central neural structures labeled MESENCEPHALON
Mesencephalic roof plate
TECTUM
(commissural GEP?)
Inferior collicular primordial plexiform layer
Inferior collicular NEP
Trochlear NEP in the isthmus
mesencephalic superventricle (future aqueduct) See enlargement on left isthmal canal
ISTHMUS
Trochlear NEP
CTF1 (fibers) CTF2 (deep neurons) CTF3 (fibers) CTF4-5? (deep neurons)
ph
er e
metencephalic pool
He
m
Uncrossed trochlear nerve (IV) fibers?
Layers of the cerebellar transitional field (CTF)
is
Ce re
b el lar NE P
Trochlear nucleus (IV)?
Premigratory inferior collicular neurons sequestered in superficial NEP? Migrating and settling isthmal neurons
Ve rm is
Migrating trochlear neurons?
Brain surface (heavier line)
CEREBELLUM Metencephalic roof plate (upper rhombic lip)
rhombencephalic superventricle (future fourth ventricle)
RHOMBENCEPHALON
Myelencephalic roof plate
MEDULLA
(lower rhombic lip)
Precerebellar NEP?
Migrating precerebellar neurons? myelencephalic pool
Migrating gracile and cuneate nuclear neurons?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Diamonds indicate symmetric areas of low cell density that are postulated to contain sprouting axons from local neurons.
Lower medullary NEP (gracile and cuneate)
Lower medullary roof plate
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
PLATE 99A GW5.5 Coronal, CR 10 mm M1000 Between Levels 2 to 4 A. Section 85
C
E B E R R A
(CEREBRAL CORTEX at higher magnification)
TELENCEPHALON AND DIENCEPHALON
L
B. Section 83
T E X O R
SEPTUM
C
(ENTIRE TELENCEPHALON)
G BA AN S G AL LI A
212
BASAL TELENCEPHALON
ER
R
S
D AN IA A L AL NG D A YG L G M A ASA B
RTEX
AM
CO
AL U
IC T P O EA E PR AR
EB
L
TH
(TELENCEPHALON AND PART OF THE DIENCEPHALON)
C
A
C. Section 123
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
See Levels 2 to 4 in Plates 86A and B to 88A and B.
213
PLATE 99B
Dorsomedial limbic cortical NEP? Primordial plexiform layer absent in roof plate
Since the cortical primordial plexiform layer has few to no cells, the migration of cortical neurons has not begun.
Telencephalic/diencephalic roof plate (primordium of choroid plexus?)
A. Section 85 B. Section 83
telencephalic superventricle
(future lateral ventricle)
Neocortical NEP
future roof of third ventricle
Cortical primordial plexiform layer
future roof of third ventricle
Neocortical NEP?
Dorsomedial limbic cortical NEP?
Less dense superficial NEP may contain sequestered premigratory Cajal-Retzius cells and subplate neurons.
telencephalic superventricle
(future lateral ventricle) Ventrolateral limbic cortical NEP? Corticoganglionic NEP Telencephalic floor plate (lamina terminalis?)
The neuroepithelium (NEP) in the telencephalon is "stockbuilding" neuronal precursors and is expanding the shoreline of the telencephalic superventricle.
Anterolateral ganglionic NEP
Septal NEP? Basal telencephalic NEP
Pioneer migrating basal ganglia neurons Less dense superficial NEP may contain sequestered premigratory neurons. Pioneer migrating septal and basal telencephalic neurons*
C. Section 123
The NEP in the diencephalon is "unloading" postmitotic neurons and the shoreline of the diencephalic superventricle is shrinking. *The basal telencephalic migrating neurons may contain mitral cells heading for the future olfactory evagination.
Sequstered and pioneer migrating anterior thalamic neurons? Cortical primordial plexiform layer
Anterior thalamic NEP
Premigratory Cajal-Retzius cells and subplate neurons sequestered in superficial cortical NEP?
diencephalic superventricle
(future third ventricle)
Preoptic NEP Lateral area? Medial area?
Diencephalic floor plate
foramen of monro
telencephalic superventricle
(future lateral ventricle)
Neocortical and limbic cortical NEP
Strionuclear NEP? Amygdaloid NEP? Corticoganglionic NEP? Sequestered and migrating posterior basal ganglia neurons? Posterior ganglionic NEP? Sequestered and migrating amygdaloid neurons? Sequestered and migrating strial bed nuclear neurons? Sequestered and migrating lateral preoptic area neurons? Sequestered and migrating medial preoptic area neurons?
214
PART PARTVIII: VIII: GW5.5 GW5.5 SAGITTAL SAGITTAL
Carnegie Collection specimen #6516 (designated here as C6516) with a 10.5 mm crown-rump length (CR) is estimated to be at gestational week (GW) 5.5. C6516 was fixed in corrosive acetic acid, embedded in a celloidin/ paraffin mix, and was cut in 8-µm sagittal sections that were stained with aluminum cochineal. Various orientations of the computer-aided 3-D reconstruction of M1000’s brain are used to show the gross external features of a GW5.5 brain (Figure 7). Like most sagittally cut specimens, C6516’s sections are not parallel to the midline; Figure 7 shows the approximate rotations in front (B) and back views (C). We photographed 65 sections at low magnification from the left to right sides of the brain. Five of the sections, mainly from the left side of the brain, are illustrated in Plates 100AB to 104AB. Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify the approximate midline, non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (lowcontrast images) identify central neural structures. Plates 105AB to 114AB show high-magnification views of many parts of the developing brain. The telencephalon is the smallest major brain structure, composed mainly of a “stockbuilding” neuroepithelium surrounding an expanding telencephalic superventricle. The primordial plexiform layer consists of discontinuous cell-sparse areas. The cortical neuroepithelium nearly reaches the pial surface with some of its outermost feathered edges. It is postulated that the superficial cortical neuroepithelium has postmitotic Cajal-Retzius cells sequestered there prior to migration. Few migrating neurons are adjacent to the very thick basal ganglionic and basal telencephalic neuroepithelia; nevertheless, these neuroepithelia are beginning to form mounds in the floor of the telencephalon. The olfactory epithelium is well established in the nasal cavity and olfactory nerve fibers are growing toward the brain. The diencephalon is the larger forebrain structure. The “stockbuilding” neuroepithelium surrounds a dorsally expanding superventricle in the future thalamic area. The thick neuroepithelium in the hypothalamic and subthalamic areas is depleting its population of stem cells and post-
mitotic, premigratory neurons are postulated to be sequestered in its superficial parts. Some migrating and settling young neurons are outside the neuroepithelium in the ventral diencephalic parenchyma adjacent to a thin subpial fibrous band. The mesencephalon, a prominent arch between the mesencephalic and diencephalic flexures, is relatively smaller than at GW6.5. The roof (tectum and pretectum) of the mesencephalon contains a stockbuilding neuroepithelium adjacent to a thin cell-sparse layer. In contract to the GW6.5 specimens, fibers in the posterior commissure are absent. The tegmental and isthmal neuroepithelia are rapidly unloading their neuronal progeny in dense bands in the adjacent parenchyma. The outermost clumps of young neurons appear to interact with axons in the subpial fiber band. The rhombencephalon is the largest brain structure. Both the pons and medulla have neuroepithelia that form crescent-shaped rhombomeres in lateral areas. In the sagittal plane, it is easy to see that rhombomeres are unloading their neuronal and glial progeny into parenchymal expansions at the entry zones of sensory cranial nerves V, VII, VIII, IX, and X. Neurons migrating in these areas are tentatively identified as receptors of the incoming sensory axons. For example, trigeminal nuclear neurons (mainly those in the principal sensory nucleus) are generated in rhombomere 2 and migrate outward to mingle with incoming afferents from the trigeminal ganglion. Medially, the pons and medulla contain longitudinal bands of migrating cells, but nuclear subdivisions are generally absent in the parenchyma. The genu of the facial motor nerve forms fascicles adjacent to a neuroepithelium medial to rhombomere 3, the presumptive source of neurons that will be receptive to axons of the facial ganglion. The subpial fiber band is definitely thicker in lateral areas where the axons from sensory ganglia enter the brain. As in the GW6.5 specimens, peripheral nerves have dense glia (Schwann cells), while central fiber tracts are clear. The cerebellum stands out as the most immature rhombencephalic structure. All parts of the cerebellar neuroepithelium are stockbuilding neuronal and glial stem cells. Relatively indistinct layers are in the cerebellar transitional field.
215
EXTERNAL FEATURES OF THE GW5.5 BRAIN lam
M a m m ill a r bo d y
lamus
lu m
Hy
potha
Sub
Ce
reb
ellum Upper rhombic lip
bu
A perfect sagittal cut through the brain is parallel to the midline from anterior to posterior. Based on Level 1, sections of C6516's brain rotate an estimated 2.5º counterclockwise from the anterior (B, front view) and posterior midlines (C, back view). In the sections illustrated on the following pages, anterior parts (top and left) are tilted toward the observer, while posterior parts (bottom and right) are tilted away from the observer.
di
Eye
3 s
Tha
t h alamus
y
I nf
un
2
BRAINSTEM FLEXURES
Medullary velum
o
Basal telencephalon Preoptic area
us
ganglia al s a
Inferior colliculus
hm
B
4
Ist
Cerebral cortex
gmentu
m
Te
n
Side view
Superior colliculus
Pretectum
Epithalamus
us
A.
P
1. Medullary 2. Pontine
M
3. Mesencephalic
e
4. Diencephalic
d
u
1
Superior colliculus
B.
Front view
Epithalamus
Posterior midline
C.
Superior colliculus
Back view
Spinal cord
Pretectum
Thalamus
a l l
Anterior midline
Lower rhombic lip
Inferior colliculus Isthmus
-2.5º Vermis
Ce
Cerebral cortex (occipital pole)
um ere ell isph reb Hem
Rhombic lip border
Right side
Cerebral cortex
Left side Eye
Medulla
Spinal cord Scale bars = 1 mm
Medullary velum
Left side
Figure 7. A, The lateral view of the left side of a computer-aided 3-D reconstruction of the brain and upper cervical spinal cord in M1000, the preceding GW5.5 specimen, which has a similar crown-rump length to C6516 (10 mm and 10.5 mm, respectively). External features are identified as in Figure 6B. The heavy numbered lines refer to brainstem flexures (boxed key). B, Front view of the brain in A. The angled line shows how C6516's sections rotate left (arrow) from the anterior midline. C, Back view of the brain in A. The angled line shows how C6516's sections rotate left (arrow) from the posterior midline.
Pons
Right side
-2.5º Medulla
Spinal cord
216
PLATE 100A GW5.5 Sagittal, CR 10.5 mm C6516, Level 1: Slide 11 Section 6
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
mesencephalic superventricle (future aqueduct)
Cell-dense primordial mesenchymal brain case (skin/bone)
ricle )
of s e
l latera
Medullary velum
cav i t y
Hyoid arch (II) Basal occipital bone?
x yn ar Ph
Cell-sparse superarachnoid reticulum
n um col
Body
central canal
E LIN ID M ID HT S RIG
E
Intervertebral disks
Medullary velum
LE F T SID EO F B RA IN
ral Ve r t e b
myelencephalic pool
Future larynx?
Anterior Anteriorcardinal cardinal vein vein
Body
Or al
Plates 105A and B: cerebral cortex Plates 106A and B: basal telencephalon Plates 107A and B: septum and hypothalamus Plates 108A and B: midbrain tegmentum and isthmus Plates 109A and B: isthmus and cerebellum
Mandibular arch (I)
tongue Primordia of
See the following for higher magnification views of this section.
sively more
Future sphenoid bone
Medial nasal process/ nasal septum
c t io n sh i f t s pr og re s
ventral pool
Rathke's pouch epithelium (primordium of anterior pituitary gland)
(future fourth ventricle)
(future lateral ventricle)
rhombencephalic superventricle
foramen of monro
telencephalic superventricle
metencephalic pool
Plan e
dorsal pool
Cell-sparse superarachnoid reticulum
subtha hypothal lamic/ amic pool
Pia
Frontal prominence
Cell-sparse superarachnoid reticulum
dienc epha su lic (futu perven re th t ird v ricle ent
tha lam ic p ool
Future dura (internal border of Cell-sparse superarachnoid reticulum
217 S E N C E P H M E A
te
Me se n
LO HA Th alamic NEP
EP
DIENC
Migrating subthalamic neurons
Migrating reticular formation neurons
oth
H
yp
r rio te An
Cerebellar
NEP (vermis) Cerebellar NEP
Upper rhombic lip
Medial cerebellar notch
R
Migrating hypothalamic neurons
E P
Basal Preoptic telencephalic NEP NEP Septal NEP
CTF2 (deep nuclear neurons)
e
Cer
al a m ic N EP
Middle/lateral
ebral
co
rt
i
Anterior complex
CTF1 (fibers)
Brain surface (heavier line)
NEP Subthalamic
m r
Reticular nuclear
Sprouting nerve IV among migrating trochlear neurons
Isthmal NEP
P
fo
Migrating tegmental neurons
o n t i n
yer la P NE al c
Epithalamic NEP
Inferior collicular
EP
Posterior alic (tegme nt commissure commissural eph a c GEP?
tal) N
N
e
EP
P
ec
Pr
N
E N C E P H A L E L ordial pl ex O N T m ri i
i
N
al
(t
EP lN ta
N l)
Labeled on this page: Central neural structures
c
ph
Superior colliculus collicular
PLATE 100B
L
c
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium
Mesence
O
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
H
M
per
Lamina terminalis
M
e u
Migrating reticular formation neurons
d
The preoptic NEP, hypothalamic NEP, subthalamic NEP, tegmental NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
l l
Lower rhombic lip
a r y
Migrating hypoglossal (XII) and vagal motor (X) neurons?
P
Fibrous processes
Lower N E
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Midline raphe glial structure Cell body layer
Midline raphe GEP?
Ventral
Ventral funiculus
Ventral gray Intermediate gray niculus Dorsal fu
Spinal NEP
Intermediate Dorsal
ay Dorsal gr
L N A S P I
Lower rhombic lip
R D C O
L O N H A E P N C B E
Up
Migrating preoptic neurons
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase.
O
Sprouting nerve VII adjacent to facial motor NEP?
Migrating basal telencephalic and septal neurons
Precerebellar NEP?
218
PLATE 101A GW5.5 Sagittal, CR 10.5 mm, C6516 Level 2: Slide 9, Section 14
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case)
thalamic pool
Cell-sparse superarachnoid reticulum
Cell-sparse superarachnoid reticulum
Pia
diencephalic superventricle
sub thalamic pool
(future third ventricle)
(future fourth ventricle)
ventral pool
optic recess
Lateral nasal process
Sphenoid bone
Mesenchyme associated with nerve I (olfactory)?
ye
le nc
cav
more late
Medullary velum
ep
i
ha li
ty
ng u e
c
Hyoid arch (II)
m
Mandibular arch (I)
Oral
P rimordia of to
Maxillary process
ssively
hypothalamic pool
f section shifts p Plane o rogre
(future lateral ventricle)
Frontal prominence
Medullary velum
foramen of monro
rhombencephalic superventricle
telencephalic superventricle
ral
metencephalic pool
dorsal pool
po ol
Pharynx
Arch III?
Basal occipital bone?
Cell-sparse superarachnoid reticulum
Anterior cardinal vein
n
D
um ol c al e br Ve r t
central canal central canal
M IDL
T LEF
INE
SIDE
OF
IN BRA
AN
DS
AL PI N
CO
R
219
alamic NEP?
P E
Subth P ala m i c NE
N EP
Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
O N A L P H C E
R6
e
Migrating reticular neurons? Ascending fiber tracts from spinal cord
Precerebellar NEP?
Migrating raphe neurons? Raphe nuclei NEP?
P
Ventral funiculus
Lowe r
N E
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei
Reticular NEP?
a r y l l
R5
Sprouting axons of local neurons
Ventral Lower rhombic lip
u
Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
R6
Migrating glossopharyngeal receptor (IX) neurons
d
R4
R5
M
Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion.
N
R4
Sprouting axons of local neurons
r
R3
E
R3
B
Migrating sensory neurons that will receive input from facial (VII) ganglion
Cerebellar notches
N
Th
h a l a mic
Hy p o t h
R2
Upper rhombic lip
Lateral
Medial
pe
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
Cerebellar NEP
Migrating pontine reticular formation neurons? Migrating trigeminal (V) nuclear complex neurons
Pontine
c
E
mi
Thala
DIENC
bt
N ic
a
O rt
L
lay er
co
T
Migrating subthalamic neurons
Migrating auditory and vestibular (VIII) neurons
R2
CTF2 (deep nuclear neurons)
Migrating reticular nucleus neurons
Up
PROPOSED RHOMBOMERE IDENTITIES
CTF1 (fibers)
M
Migrating ganglionic neurons
cular
O
Basal telencephalic NEP
Optic nerve GEP
o lli
H
Medial ganglionic NEP
Migrating basal telencephalicneurons
rc
Brain surface (heavier line)
Su
Cerebral
orm
P
rio
Migrating pretectal neurons
Reticular nuclear
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
R
E N C E P E L Primordial ple H A xif
ic
fe
P
am
Pretectal NEP
NEP
NE
al
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
O
N
N
N
L
Superior a l co i l
c t al)
NE
P
LO A H EP
enceph
(te
l
M
es
PLATE 101B
ar ul lic
Labeled on this page: Central neural Brain surface structures (heavier line)
M
In
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
E N C E P H A E S c
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Ventral gray
The telencephalic NEP, thalamic NEP, tectal NEP, and cerebellar NEP form expanding shorelines of the superventricle as stockbuilding NEP cells increase. The hypothalamic NEP, subthalamic NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
Ventral gray
Ventral funiculus
Intermediate gray?
Spinal NEP
Ventral gray Ventral
Dorsal
Dorsal gray
Gracile and cuneate nuclear NEP?
Intermediate
A L I N S P
R D C O
Migrating gracile and cuneate nuclear neurons?
PLATE 102A GW5.5 Sagittal, CR 10.5 mm, C6516 Level 3: Slide 8, Section 14
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-dense primordial mesenchymal brain case (skin/bone) Future dura (internal border of brain case) An card terior inal vein
Cell-sparse superarachnoid reticulum Pia
Cell-sparse superarachnoid reticulum
dorsal pool
telencephalic superventricle
metencephalic pool
(future lateral ventricle)
(optic recess)
rhombencephalic superventricle
(future fourth ventricle)
Frontal prominence
diencephalic superventricle
ventral pool
Lateral nasal process Nerve I (olfactory)?
Sphenoid bone
Nasal/olfactory epithelium Maxillary process
Vestibulocochlear ganglion (VIII)
O l
ngu e
Petrous temporal bone
Hyoid arch (II)
See higher magnification views of the rhombencephalon from this section in Plates 110A and B and Plates 111A and B.
myelencephalic pool
Otic vesicle
y cav i t
P rimordia of to
ra
Mandibular arch (I)
Arch III? Inferior vagal ganglion X?
A
Sympa
i n te r
ard or c
in a l
Cell-sparse superarachnoid reticulum vein
a k g run t c i thet
ENT I RE S E C
Medullary velum
Spinal nerves
ng
lia
FRO TI O N IS
Basal occipital bone?
?
Dorsal root ganglia
M LE
FT S
I
F DE O
BRA
IN
D AN
SP
A IN
O LC
RD
shifts progressively f section more l at era l Plane o
220
221
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
CTF3 (deep nuclear neurons and fibers)
DI
Migrating subthalamic neurons
CTF2 (deep nuclear neurons) CTF1 (fibers)
m ic N E P
NEP
Cerebellar NEP Medial Lateral
Brain surface (heavier line)
P
Strionuclear NEP?
R3
N
Optic nerve GEP
R2
P
L O N H A
Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
R7
E
R6
Sprouting axons of local neurons
P
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei
Migrating vagal sensory (X) neurons
r we Lo
R5
Precerebellar NEP?
R7
NE
Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
Lower rhombic lip
ry
R4
Migrating glossopharyngeal receptor (IX) neurons
lla
Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion.
R6
du
R3
R5
Me
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
er Upp
Migrating auditory and vestibular (VIII) neurons
R2
C
R4
Sprouting axons of local neurons
PROPOSED RHOMBOMERE IDENTITIES
E
Migrating basal ganglionic neurons
ic
tine
gli on
Cerebellar notches
Upper rhombic lip
B
Gan
Migrating trigeminal (V) nuclear complex neurons Migrating sensory neurons that will receive input from facial (VII) ganglion
Po n
N
E
Anterolateral
NE
Amygdaloid/ posterolateral P
Cereb
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Subthala
L A
l c or t
Thalamic NEP
ra
al
E P HAL
R H O M
T E L E N C E P H
ic
NC
(Posterior complex)
Primordial plexiform layer
O
E
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
ON
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Labeled on this page: Central neural structures N
PLATE 102B
MESENCEPHALON (lateral edge)
Cuneate nuclear NEP? Migrating cuneate nuclear neurons?
Ascending fiber tracts from spinal cord
Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
s iculu a l fu n Ventr
Lateral funiculus
Ventral gray
Spinal NEP Dorsal
Intermediate gray?
A L I N S P
R D C O
The telencephalic NEP, thalamic NEP, and cerebellar NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. The subthalamic NEP, pontine NEP, and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
222
PLATE 103A GW5.5 Sagittal, CR 10.5 mm, C6516 Level 4: Slide 7, Section 10
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cell-dense primordial mesenchymal brain case (skin/bone) Cell-sparse superarachnoid reticulum Pia
Nasal cavity
(future fourth ventricle)
myelencephalic pool
Nerve VIII
A n t e r boundary cap*
Nerve VIII
Maxillary process
Nasal epithelium
rhombencephalic superventricle
P r i m o r di
Placodal epithelium Oral cavity
Vestibulocochlear ganglion (VIII)
a of
Mandibular arch (I)
eral
Lateral nasal process
io
Choroid fissure
Medullary velum
to n
*Boundary caps are Schwann cell GEPs?
Petrous temporal bone
gu
l at more y l e v i s s P la n e of section shifts progre
Nerve I (olfactory) Olfactory epithelium
Nerve II
metencephalic pool
Nerve V boundary cap*
Otic vesicle
Ne rv eI X
(future lateral ventricle, lateral pool)
r cardinal vein
telencephalic superventricle
e
Nerve II (optic)
Hyoid arch (II)
Nerve V (trigeminal) Nerve VIII (vestibulocochlear)
Nerve X boundary cap*
Arch III?
Nerve IX (glossopharyngeal)
Nerve X al Superior din r a ganglion (X) rcn Basal o i ter vei occipital An bone?
Arch IV?
Nerve X (vagus)
See a higher magnification view of the rhombencephalon from a nearby section in Plates 112A and B.
Sympathe
Inferior ganglion (IX) Inferior ganglion (X)
tic
n k ga trun
Do
EN T
gli
a?
l rsa
IRE
roo
SEC
t g
TI
g an
lia
SF ON I
L ROM
EF
ID TS
EO
F
A BR
IN
AN
P DS
AL IN
CO
RD
223
PLATE 103B
Labeled on this page: Central neural structures FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from germinal sources.
N
tical N or
al
G a n gli o
Sprouting olfactory nerve (I) axons
n ic
N
Migrating basal ganglionic neurons Optic nerve GEP
Cerebellar NEP Cerebellar notches
R2
Pontine NEP Central trigeminal tract Migrating auditory and vestibular (VIII) neurons
R4
Lateral lemniscus
R5
Medullary NEP
Lower rhombic lip
L
R6
N
R7
O
Migrating vestibulocochlear (VIII) ganglionic neurons from germinal source in otic vesicle epithelium
A
Peripheral neural structures
Migrating glossopharyngeal (IX) ganglionic neurons from germinal source in glossopharyngeal placode
Upper rhombic lip
Lateral
Medial
Migrating trigeminal (V) nuclear complex neurons?
EP
Ce
CTF3 (deep nuclear neurons and fibers)
Primary olfactory cortical NEP? Posterolateral/ amygdaloid Anterolateral
CTF2 (deep nuclear neurons)
B E H N C E P
TELE
Brain surface (heavier line)
CTF1 (fibers)
R H O M
NCEP
re
br
HA
Primordial plexiform layer
EP
c
L
O
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Migrating glossopharyngeal sensory (IX) neurons Migrating vagal sensory (X) neurons
Migrating vagal (X) ganglionic neurons from germinal source in vagal placode?
PROPOSED RHOMBOMERE IDENTITIES
The telencephalic NEP and cerebellar NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. The pontine NEP and medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
R2
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
R4
Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
R5
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei
R6
Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
R7
Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
224
PLATE 104A GW5.5 Sagittal, CR 10.5 mm, C6516 Level 5: Slide 6, Section 15
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Neural retina Retinal NEP
Cell-dense primordial mesenchymal brain case (skin/bone)
EYE
Intraretinal space Pigment layer Pigment epithelium of retina
Pia
Trigeminal ganglion (V)
Nerve V
telencephalic superventricle
Nerve V boundary cap*
Anterior cardinal vein
(future lateral ventricle, lateral pool)
metencephalic pool
rhombencephalic superventricle
(future fourth ventricle)
Nerve II
Nasal cavity
Maxillary process
Nasal epithelium
myelencephalic pool
Facial ganglion (VII)?
Vestibulocochlear ganglion (VIII)
Maxillary placodal epithelium
Oral cavity Mandibular arch (I)
Nerve II (optic) Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
Nerve X
Lingual epithelium
Superior vagal ganglion (X)
Hyoid arch (II) Inferior ganglion (IX)
Anterior cardinal vein
Arch IV?
sup Celler spa ret arach rse icu no lum id
*Boundary caps are Schwann cell GEPs?
Otic vesicle
Petrous temporal bone
E
O
F
BR
AI
N
See higher magnification views of the rhombencephalon from nearby sections in Plates 112A and B to Plates 114A and B.
SI
D
ENT
S IRE
EC
TIO
S NI
OM FR
F LE
T
P l ane o f s e c ti o n s h ift s
Lateral nasal process
Medullary velum Nerves VII+VIII boundary caps* Nerves VII+VIII
eral re lat
Choroid fissure
ly mo essive progr
Nerve I (olfactory) Olfactory epithelium
225
PLATE 104B
Labeled on this page: Central neural structures FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
b re
r
y
a ry olf a c
to
Migrating trigeminal (V) nuclear complex neurons? Central trigeminal tract (devoid of glia)
cerebellar notch
Upper rhombic lip
Medial cerebellar notch
R2 Migrating primary olfactory cortex neurons Migrating Cajal-Retzius neurons Migrating auditory and Optic vestibular (VIII) neurons nerve Lateral lemniscus GEP (devoid of glia) Peripheral nerves have dense glia.
EP rN lla here) e eb isp Lateral
r m Ce (he
Brain surface (heavier line)
P ri m
TEL
CTF2 (deep nuclear neurons)
Pontine NEP R4
Medullary NEP R5
Lower rhombic lip
RH O M BEN CE P H A L O N
Ce
AL
l
CTF1 (fibers)
co r t ical
EP
ENCEPH
ra
Primordial plexiform layer
N
ON
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Arrows indicate the presumed direction of neuron migration from germinal sources.
Migrating vestibulocochlear (VIII) ganglionic neurons from germinal source in otic vesicle epithelium
PROPOSED RHOMBOMERE IDENTITIES R2
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
R4
Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
R5
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
The telencephalic NEP and cerebellar NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. The pontine NEP and medullary NEP form shrinking shorelines of the superven-tricle as stockbuilding NEP cells decrease.
Migrating auditory and vestibular (VIII) neurons
Migrating vagal sensory (X) neurons
See Level 1 in Plates 100A and B.
GW5.5 Sagittal, CR 10.5 mm, C6516 Level 1: Slide 11, Section 6 DORSAL CEREBRAL CORTEX
226
PLATE 105A
Primordial mesenchymal brain case (skin/bone/dura/arachnoid)
Brain surface (heavier line)
Future pia
The subarachnoid reticulum is indistinguishable over the cortex.
Earliest migrating Cajal-Retzius cells The superficial cerebral cortical NEP is postulated to contain postmitotic, premigratory CajalRetzius cells.
The primordial plexiform layer forms discontinuous cell-sparse areas outside the cerebral cortical NEP.
Synthetic zone
telencephalic superventricle (future lateral ventricle)
Mitotic NEP cells NEP - neuroepithelium The cerebral cortical NEP is in the "stockbuilding" phase when neural stem cells are increasing and few neurons (CajalRetzius cells) are being generated.
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Mitotic zone
Pseudostratified NEP
P pre ostmit m o neu igratotic ron ry, s?
Cerebral cortical NEP
PLATE 105B
227
See Level 1 in Plates 100A and B.
GW5.5 Sagittal, CR 10.5 mm, C6516 Level 1: Slide 11, Section 6 BASAL TELENCEPHALON
228
PLATE 106A
PLATE 106B
Postmitotic, premigratory neurons?
Frontal prominence
Synthetic zone Mitotic zone
Mitotic NEP cells
Primordial plexiform layer
Cerebral cortical NEP
telencephalic superventricle (future lateral ventricle)
ventral pool
Basal telencephalic NEP
Brain surface (heavier line)
Septal NEP
Mitotic zone Synthetic zone
Pioneer migrating basal telencephalic neurons
Medial nasal process/ nasal septum
NEP - neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Differentiating field
Pioneer migrating septal neurons
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
229
See Level 1 in Plates 100A and B.
GW5.5 Sagittal, CR 10.5 mm, C6516 Level 1: Slide 11, Section 6 SEPTUM/DIENCEPHALON
230
PLATE 107A
PLATE 107B
Successive waves of migrating hypothalamic neurons
NEP - neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
foramen of monro
telencephalic superventricle (future lateral ventricle)
diencephalic superventricle
Middle/lateral hypothalamic NEP
Brain surface (heavier line)
(future third ventricle) hypothalamic pool
ventral pool
Septal NEP
Preoptic NEP
Anterior hypothalamic NEP
Migrating hypothalamic neurons
Pioneer migrating septal neurons
Pioneer migrating preoptic neurons
Lamina terminalis (closure site of anterior neuropore)
Rathke's pouch epithelium (primordium of anterior pituitary gland) Sphenoid bone
Sphenoid bone Oral epithelium Oral cavity
231
GW5.5 Sagittal, CR 10.5 mm, C6516 Level 1: Slide 11, Section 6 MIDBRAIN TEGMENTUM See Level 1 in Plates 100A and B.
232
PLATE 108A
PLATE 108B
NEP - neuroepithelium
mesencephalic superventricle
e
s
c n e
e
ta
l)
N
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
E
P
M
(future aqueduct)
lic (tegme n pha
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Mitotic NEP cells
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Blood islands and blood vessel primordia invade NEP
Successive waves of migrating tegmental neurons
Subthalamic NEP
Predominantly longitudinal fiber tracts
Cell-sparse superarachnoid reticulum Successive waves of migrating subthalamic neurons Brain surface (heavier line)
Migrating isthmal neurons Brain surface (heavier line)
Isthmal NEP
233
234
PLATE ?A 109A GW5.5 Sagittal, CR 10.5 mm, C6516 Level 1: Slide 11, Section 6 ISTHMUS and CEREBELLUM See Level 1 in Plates 100A and B.
235
PLATE 109B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Upper rhombic lip
ABBREVIATIONS: CTF - Cerebellar transitional field NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
mis) CTF2 (deep nuclear neurons)
Cere
CTF1 (fibers)
(ver P r NE bella
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Lateral cerebellar notch
rhombencephalic superventricle
(future fourth ventricle) metencephalic pool
Mitotic NEP cells
Brain surface (heavier line)
Migrating inferior collicular neurons?
Medial cerebellar notch
Migrating trochlear (IV) neurons? Sprouting nerve IV axons?
Mesencephalic (tectal, inferior collicular) NEP
Isthmal NEP Mitotic NEP cells
mesencephalic superventricle (future aqueduct)
Mesencephalic (tegmental) NEP
Blood islands and blood vessel primordia invade NEP rac ib e r t f rons? l u a e n n tu d i mal lo n g i g isth y l n t i t n a a Migr o m in P red
ts
A higher magnification view of the R2 to R7 neuroepithelium is in Plates 111A and B. See Level 3 in Plates 102A and B.
GW5.5 Sagittal, CR 10.5 mm, C6516 Near Level 3: Slide 8, Section 10 PONS/MEDULLA
236
PLATE 110A
FONT KEY: R2 ventricular divisions - capitals Germinal zone - Helvetica bold R3 Transient structure - Times bold italic Permanent structure - Times Roman or Bold R4 ABBREVIATIONS: R5 CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R6 R - Rhombomere R7 CTF3
(deep nuclear neurons and fibers)
PROPOSED RHOMBOMERE IDENTITIES Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Migrating cuneate nuclear neurons? Lower rhombic lip
Precerebellar NEP?
CTF2 (deep nuclear neurons) Upper rhombic lip
Cuneate nuclear NEP?
E
P
CTF1 (fibers)
Lo we r
PLATE 110B
Medullary velum
NEP
Lateral cerebellar notch
rhombencephalic superventricle
myelencephalic pool
M
Sprouting axons of local neurons
e
r lla
metencephalic pool
(future fourth ventricle)
b re
U
e
Medial cerebellar notch
C
P o n t i n e
N
R2
E
P R3
r ppe
e
d
u
a l l
r
y
N
Ascending fiber tracts from spinal cord
R7
Sprouting axons of local neurons
R6
Migrating vagal sensory (X) neurons
R5
Migrating glossopharyngeal receptor (IX) neurons
R4
Anterior cardinal vein
Ganglion VIII boundary cap (Schwann cell GEP?) Vestibulocochlear ganglion (VIII)
Otic vesicle
Petrous temporal bone Inferior ganglion (X)
Brain surface (heavier line) Hyoid arch (II) Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Migrating trigeminal (V) nuclear complex neurons neurons?
Migrating sensory Migrating auditory and vestibular (VIII) neurons neurons that will receive input from facial(VII) (VII)ganglion? ganglion facial
Arch III
Oral cavity/pharynx
237
R2 R3 R4 R5 R6 R7
PROPOSED RHOMBOMERE IDENTITIES Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
See Level 3 in Plates 102A and B.
GW5.5 Sagittal, CR 10.5 mm, C6516 Near Level 3: Slide 8, Section 10 PONS/MEDULLA
238
PLATE 111A
PLATE 111B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
U p p e r
m e d u l l a r y
rhombencephalic superventricle
Blood islands and blood vessel primordia invade NEP
(future fourth ventricle)
P o n t i n e
N E P
R7
R6
R5
R2
R3
(sensory IX neuronal NEP)
(sensory X neuronal NEP)
(vestibuloauditoryNEP)
R4
(trigeminal NEP)
N E P
(vestibuloauditoryNEP)
(facial sensory NEP) Sprouting axons of local neurons
Migrating trigeminal (V) nuclear complex neurons Brain surface (heavier line)
Migrating sensory neurons that will receive input from facial (VII) ganglion
Sprouting axons of local neurons
Migrating glossopharyngeal receptor (IX) neurons Migrating vestibular and auditory (VIII) neurons Ganglion VIII boundary cap (Schwann cell GEP?)
Migrating vestibular and auditory (VIII) neurons
Migrating vagal sensory (X) neurons?
Vestibulocochlear ganglion (VIII)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
239
240
PLATE 112A
GW5.5 Sagittal, CR 10.5 mm, C6516 Between Levels 4 and 5: Slide 7, Section 6 RHOMBENCEPHALON See Level 4 in Plates 103A and B; Level 5 in Plates 104A and B. PROPOSED RHOMBOMERE IDENTITIES R2 R4 R5 R6 R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
241
PLATE 112B
CTF3 (deep nuclear neurons and fibers) CTF2 (deep nuclear neurons) CTF1 (fibers)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
P
Upper rhombic lip
metencephalic pool
Peripheral nerves and boundary caps are filled with string-like arrays of Schwann cells, but all internal fiber tracts are free of interstitial glia. Apparently peripheral nerve gliogenesis precedes central fiber tract gliogenesis.
Medullary velum
Boundary caps may be the germinal sources (glioepithelia) of Schwann cells.
Medial cerebellar notch rhombencephalic superventricle
Wherever peripheral afferents enter the central nervous system, there is a swelling of the superficial fiber tracts to accommodate the larger number of axons at these sites.
(future fourth ventricle)
R2
Pontine NEP
Mi
Nerve V boundary cap
Central trigeminal tract Lateral lemniscus
Anterior cardinal vein
R4 vesti bular
Mandibular arch (I) Mandibular placodal epithelium
R6 Migrating glossopharyngeal sensory (IX) neurons
Nerve VIII boundary cap
R7
Migrating vagal sensory (X) neurons?
Glossopharyngeal afferent fibers
Vagal Nerve X afferent boundary cap fibers
Nerve IX boundary cap
Lumen
Otic vesicle
Arrows indicate the presumed direction of neuron migration from germinal sources.
neu ron s
Epithelium
Oral cavity
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
and auditory (V I I I)
Vestibulocochlear ganglion (VIII)
Maxillary process
Maxillary placodal epithelium
R5
Superior vagal ganglion (X)
e I X
Nerve V
ti ng
Medullary NEP
rv
Tr i ga gem n g in (V lio n a l )
g ra
Lower rhombic lip
myelencephalic pool
Ne
Migrating trigeminal (V) nuclear complex neurons
Petrous temporal bone
Pharynx
Inferior glossopharyngeal ganglion (IX)
Arch III? Hyoid arch (II)
X
Brain surface (heavier line)
Ne rv e
N
er
r
Lateral cerebellar notch
sph
lla
(hemi
Cerebe
e)
E
ABBREVIATIONS: CTF - Cerebellar transitional field NEP - Neuroepithelium R - Rhombomere
Schwann cell arrays in the vagus nerve (These arrays are present in all peripheral nerves and boundary caps.)
Anterior cardinal vein
Placodal germinal source of ganglion IX?
242
PLATE ?A 113A
GW5.5 Sagittal, CR 10.5 mm, C6516 Lateral to Level 5: Slide 6, Section 11 RHOMBENCEPHALON See Level 5 in Plates 104A and B. See level 5 in Plates ?? A and B. PROPOSED RHOMBOMERE IDENTITIES R2 R4
See Plates ?? A and 114A and B. B.
R5
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
243
PLATE PLATE 113B ?B
Upper rhombic lip
ABBREVIATIONS: CTF - Cerebellar transitional field NEP - Neuroepithelium R - Rhombomere
r N EP he r
CTF1 (fibers)
e)
CTF2 (deep nuclear neurons)
metencephalic pool
Brain surface (heavier line)
As seen in Plates 112A and B, peripheral nerves are filled with stringlike arrays of Schwann cells, while internal fiber tracts are free of interstitial glia. The boundary caps of these nerves may be the germinal sources (glioepithelia) of Schwann cells.
isp
(hem
Cereb
ella
CTF3 (deep nuclear neurons and fibers)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medullary velum
The swellings at the entry zones of the trigeminal and vestibulocochlear nerves are especially prominent in this section. Evidently, massive numbers of fibers are entering the central nervous system myelensimultaneously. cephalic pool
rhombencephalic superventricle
(future fourth ventricle)
Cerebellar notch
Migrating trigeminal (V) nuclear complex neurons Nerve V boundary cap
Nerve V (opthalmic branch)
R2
Nerve V (trigeminal)
mi na
ga
l
nglion (V)
n d a ud
Lower rhombic lip
Cochlear nuclear NEP?
itory neuro s n
Migrating cochlear nuclear neurons?
Nerve VIII boundary cap
Vestibular and auditory afferent fibers
Neural retina (retinal NEP)
Facial ganglion (VII)? Epithelium
Oral cavity
Pe
tr
ne
Lumen
Otic vesicle
bo
Choroid fissure
Superior glossopharyngeal ganglion (IX)
l
Optic nerve GEP
Vestibulocochlear ganglion (VIII)
ou
or
a
Anterior cardinal Nerve VIII vein with many intersitial Schwann cells
Glial channels in Retinal NEP?
M ax ill ar yp ro ce ss
EYE
lar a
R5
Trigeminal afferent fibers
ge Intraretinal space
Medullary NEP
R4
Migr a tin g ve sti b u
Tr i
Pigment epithelium
Pontine NEP
s te mp
Mandibular arch (I) Arrows indicate the presumed direction of axon growth in brain fiber tracts. Arrows indicate the presumed direction of neuron migration from germinal sources.
Maxillary placodal epithelium
Anterior cardinal vein
Hyoid arch (II) Lingual epithelium
244
PLATE 114A
GW5.5 Sagittal, CR 10.5 mm, C6516 Lateral to Level 5: Slide 6, Section 11 ENTRY ZONES OF NERVES V AND VIII
See Level 5 in Plates 104A and B. PROPOSED RHOMBOMERE IDENTITIES
R2 R4
R5
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
245
PLATE 114B
CTF1 (fibers)
Cerebellar NEP
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
(hemisphere)
CTF2 (deep nuclear neurons)
CTF3 (deep nuclear neurons and fibers)
ABBREVIATIONS: CTF - Cerebellar transitional field NEP - Neuroepithelium R - Rhombomere
Cerebellar notch
Pontine NEP
Migrating trigeminal (V) nuclear complex neurons
rhombencephalic superventricle
Medullary velum
(future fourth ventricle)
R2
Medullary NEP
R4 Mig
ve V Ne r
Trigeminal afferent fibers
bo
un
da
ry
rat
ing
ves
R5 tib
cap
glio i
neurons
g nal
Vestibular and auditory afferent fibers
Nerve VIII boundary cap
an
Tr i g e m
r and auditory
n (V)
Nerve V with many intersitial Schwann cells
ula
These neurons carry primary sensory information from touch and pressure receptors in the face.
Vestibular ganglion? (primary sensory information from maculae of the semicirular canals, utricle, and saccule)
Nerve VIII with many intersitial Schwann cells
Anterior cardinal vein
Boundary caps may be the germinal sources (glioepithelia) of Schwann cells.
Arrows indicate the presumed direction of axon growth in brain fiber tracts. Arrows indicate the presumed direction of neuron migration from germinal sources.
Vestibulo-cochlear ganglion (VIII) Facial ganglion (VII)? (primary sensory information from the taste buds of the anterior tongue)
Maxillary process
Oral cavity
Lumen
Spiral ganglion? (primary sensory information from the cochlea)
Otic vesicle Epithelium
(germinal source of vestibulocochlear ganglionic neurons)
Petrous temporal bone surrounds otic vesicle.
246
PART PARTIX: IX: GW5 GW5 CORONAL CORONAL
Carnegie Collection specimen #8314 (designated here as C8314) with a 7.1 mm crown-rump length (CR) is estimated to be at gestational week (GW) 5. C8314 was fixed in formalin, embedded in a celloidin/paraffin mix, and was cut in 8 µm transverse sections that were stained with azan. Sections of the prosencephalon and anterior mesencephalon are cut in the coronal plane, but the plane shifts to predominantly horizontal in the posterior mesencephalon, pons and medulla. We photographed 39 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and rhombencephalon. Eleven of these sections are illustrated in Plates 115AB to 124AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of C8314’s brain and eye (Figure 8), and to show each illustrated section in situ (insets, Plates 115A to 124A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural and peripheral neural structures; labels in B Plates (lowcontrast images) identify central neural structures. At this stage of development, the forebrain is a unitary prosencephalon because a telencephalon cannot be clearly distinguished from the diencephalon. There are no paired telencephalic vesicles. The most anterior brain sections are tentatively identified as the future telencephalon, while sections of the optic vesicle and posterior to it are more clearly identified as diencephalic. All parts of the prosencephalic neuroepithelium are rapidly increasing their pool of neuronal and glial stem cells as they expand the shorelines of the enlarging prosencephalic superventricle. Cell migration is virtually absent. The olfactory placode has not yet invaginated, but forms a thick epithelium in the anterolateral surface of the head. The evaginated optic vesicle forms a C-shaped curve around the developing lens,
defining an inner retinal neuroepithelium and an outer pigment epithelium. The eye is much closer to the diencephalon than at GW5.5 (Part VII) and does not yet form a stalk-like extension that will be the optic nerve. The mesencephalon contains a stockbuilding neuroepithelium in the pretectum and tectum; cell migration has not yet begun. The tegmental and isthmal neuroepithelia are also stockbuilding their stem cell populations. Only a few pioneer neurons have migrated out. The subpial fiber band is very thin in the tegmentum, but thickens slightly in the isthmus. The most prominent neuroepithelial structures in the rhombencephalon are the laterally-placed rhombomeres. These are crescent-shaped evaginations of stockbuilding neuroepithelium separated by narrow mounds jutting into the ventricular lumen. Blood islands and sprouting pioneer axons form clefts in between the evaginations. The rhombomeres are associated with the entry zones of sensory cranial nerves V, VII, VIII, IX, and X. In the coronal plane, the trigeminal ganglion (sensory axons of V) can be easily associated with rhombomere 2, and the vestibulocochlear ganglion (source of VIII axons) with rhombomeres 4 and 5. The subpial fiber band is thicker where sensory afferent axons enter the brain. A thin, definite layer of migrating neurons lines the superficial border of each rhombomere as neuronal and glial progeny move into a small parenchyma. Medial pontine and medullary neuroepithelia are thinner, and may actually be shrinking as more neurons and glia migrate outward. The small stockbuilding cerebellar neuroepithelium is only identifiable in the most posterior sections of the rhombencephalon; the few neurons accumulating outside it are probably the earliest-generated deep nuclear neurons.
247
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C8314 Computer-aided 3-D Brain Reconstructions B.
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Figure 8. A, The left side of the 3-D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
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248
PLATE 115A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 1: Section 12
Primordial mesenchymal brain case (skin, bone, and meninges)
Pia and pial blood islands
Frontonasal process Olfactory placode Maxillary process
Level 1: Computer-aided 3-D Brain Reconstruction
Level 2: Section 42 Primordial mesenchymal brain case (skin, bone, and meninges)
Pia and pial blood islands
Frontonasal process
Pioneer olfactory nerve (I) fibers Olfactory placode Maxillary process
Level 2: Computer-aided 3-D Brain Reconstruction
249
PLATE 115B
Central neural structures labeled
Level 1: Section 12 ANTERIOR PROSENCEPHALON Brain surface (heavier line)
Prosencephalic roof plate
Prosencephalic primordial plexiform layer
prosencephalic superventricle
Prosencephalic NEP
(future lateral and third ventricles)
(future telencephalic)
Prosencephalic floor plate
ANTERIOR PROSENCEPHALON
Level 2: Section 42
Prosencephalic roof plate
Brain surface (heavier line)
Prosencephalic NEP (future thalamic)
Prosencephalic primordial plexiform layer
Prosencephalic NEP (future telencephalic)
prosencephalic superventricle
(future lateral and third ventricles)
Prosencephalic NEP
(future preoptic/hypothalamic)
Prosencephalic floor plate NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
250
PLATE 116A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 3: Section 82
Blood islands in developing pia
Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing dura
Formative superarachnoid reticulum Invaginating lens placode
EYE Intraretinal space Retinal NEP Lens vesicle Choroid fissure Pigment epithelium
Rathke's pouch?
Cephalic (maxillary) placode
Oral cavity
Maxillary process
Primordium of mandible Mandibular arch (I)
Primordium of tongue Lateral swellings Medial swellings
Hyoid arch (II)
Level 3: Computer-aided 3-D Brain Reconstruction
Arch III Arytenoid swellings
Arch IV
Larynx
Pharynx Vagal ganglion (X) Nerve X (vagus)
Glottis
Sympathetic trunk
The GW5 Face and Neck
Figure 247B modified (Patten, 1953, p. 429.)
Frontonasal process
Oral cavity
Eye Olfactory placode Maxillary process
Mandible Hyo-mandibular cleft
Mandibular arch Hyoid arch Arches III and IV
251
PLATE 116B
Central neural structures labeled
Thalamic primordial plexiform layer
THALAMUS Diencephalic roof plate
Brain surface (heavier line)
Thalamic NEP SUBTHALAMUS diencephalic superventricle
Subthalamic NEP PREOPTIC AREA/ HYPOTHALAMUS Preoptic NEP
(future third ventricle)
Subthalamic primordial plexiform layer Preoptic primordial plexiform layer
Retinal NEP optic recess
Preoptic/hypothalamic NEP Diencephalic floor plate
infundibular recess
Preoptic/hypothalamic primordial plexiform layer
DIENCEPHALON
Non-neural structures Lingual epithelium
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
252
PLATE 117A GW5 Coronal CR 8 mm C8314 Level 4: Section 97
Peripheral neural and non-neural structures labeled Blood islands in developing pia Blood islands in developing dura
Primordial mesenchymal brain case (skin, bone, and meninges)
Formative superarachnoid reticulum
EYE Intraretinal space
Rathke's pouch epithelium (primordium of adenohypophysis)
Retinal NEP Lens vesicle Choroid fissure Pigment epithelium
Oral cavity
Maxillary process
Cephalic (maxillary) placode
Mandibular arch (I)
Primordium of mandible Primordium of tongue Lateral swellings Medial swellings
Hyoid arch (II) Arch III Arytenoid swellings
Arch IV
Larynx Glottis
Pharynx
Vagal ganglion (X) Nerve X (vagus) Sympathetic trunk
Level 4: Computer-aided 3-D Brain Reconstruction
253
PLATE 117B
Central neural structures labeled DIENCEPHALON Diencephalic roof plate
EPITHALAMUS (primordium of pineal gland) Epithalamic NEP THALAMUS
Epithalamic/thalamic primordial plexiform layer pineal recess
Brain surface (heavier line)
Thalamic NEP SUBTHALAMUS Subthalamic NEP
diencephalic superventricle
Subthalamic primordial plexiform layer
(future third ventricle)
PREOPTIC AREA/ HYPOTHALAMUS Preoptic NEP?
Preoptic(?) primordial plexiform layer
Retinal NEP Anterior hypothalamic NEP
infundibular recess Hypothalamic primordial plexiform layer
Diencephalic floor plate (primordium of median eminence)
Non-neural structures Lingual epithelium
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
PLATE 118A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 5: Section 117 Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing pia Blood islands in developing dura
Formative superarachnoid reticulum
Internal carotid artery?
Sp he no id pr im or diu m?
254
Anterior cardinal vein?
ss ) ce ch ro ar y p ular r a ill dib ax n M s ma n i (jo
Rathke's pouch epithelium (primordium of adenohypophysis) Maxillary/mandibular placode
Oral cavity Lateral primordium Medial primordium of tongue of tongue
Ganglion IX placode Ganglion IX
Mandibular arch (I) Hyoid arch (II)
Arch III
Epiglottis Pharynx
Vagal ganglion (X) Anterior cardinal vein?
Nerve X
Notochord
Level 5: Computer-aided 3-D Brain Reconstruction
255
PLATE 118B
Central neural structures labeled MESENCEPHALON PRETECTUM
Mesencephalic roof plate (posterior commissural GEP)
mesencephalic superventricle (future aqueduct)
Pretectal/thalamic primordial plexiform layer
Pretectal NEP
Brain surface (heavier line)
THALAMUS Thalamic NEP
SUBTHALAMUS
diencephalic superventricle (future third ventricle)
Subthalamic NEP HYPOTHALAMUS Anterior/middle hypothalamic NEP Diencephalic floor plate (primordium of median eminence and neurohypophysis)
Subthalamic primordial plexiform layer infundibular recess
Hypothalamic primordial plexiform layer
DIENCEPHALON
Non-neural structure Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
256
PLATE 119A GW5 Coronal CR 8 mm C8314 Level 6: Section 127
Peripheral neural and non-neural structures labeled Blood islands in developing dura
Primordial mesenchymal brain case (skin, bone, and meninges)
Formative superarachnoid reticulum Anterior cardinal vein?
Sp he no id pr im or diu m?
Blood islands in developing pia
Circle of Willis arteries? Anterior cardinal vein?
Notochord
Fused maxillary process and mandibular arch
Nerve V?
Meckel's cartilage
Branchial placodes Glossopharyngeal ganglion (IX)
Hyoid arch (II)
l bone tempora Petrous
Notochord
Pharynx
Nerve IX (glossopharyngeal) Nerve X (vagus) Anterior cardinal vein?
Level 6: Computer-aided 3-D Brain Reconstruction
257
PLATE 119B
Central neural structures labeled MESENCEPHALON
Mesencephalic roof plate (posterior commissural GEP)
PRETECTUM
Posterior commissure pioneer fibers
Pretectal NEP
Pretectal/tectal primordial plexiform layer
TECTUM
Tectal (superior collicular) NEP TEGMENTUM
Tegmental NEP
HYPOTHALAMUS
Hypothalamic (mammillary) NEP Diencephalic floor plate
DIENCEPHALON
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
mesencephalic superventricle (future aqueduct)
Brain surface (heavier line)
Tegmental primordial plexiform layer Pioneer migrating tegmental neurons
Mammillary primordial plexiform layer
diencephalic superventricle
(future third ventricle, mammillary recess)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
PLATE 120A GW5 Coronal CR 8 mm C8314 Level 7: Section 162
Peripheral neural and non-neural structures labeled Blood islands in developing dura
Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing pia
Cell-sparse superarachnoid reticulum
Basilar artery
Anterior cardinal vein
Trigeminal ganglion (V)
Nerve V (trigeminal) Anterior cardinal vein Vestibulo-cochlear ganglion (VIII)
Otic vesicle Lumen
b one
Epithelium
Pe
r al
258
trous temp o
Nerve and ganglion IX (glossopharyngeal)
Nerve and ganglion X (vagal)
Level 7: Computer-aided 3-D Brain Reconstruction
259
PLATE 120B
Central neural structures labeled MESENCEPHALON
Brain surface (heavier line)
TECTUM
Superior collicular primordial plexiform layer
Mesencephalic roof plate mesencephalic superventricle
Tectal (superior collicular) NEP
(future aqueduct)
TEGMENTUM
Tegmental NEP
Tegmental primordial plexiform layer
Mesencephalic floor plate
Pioneer migrating tegmental neurons
Midline raphe glial structure
PONS
Medial lemniscus?
Pontine floor plate
(midline raphe glial structure GEP)
Sequential waves of migrating pontine neurons
Medial pontine NEP
Peripheral neural structure
rhombencephalic superventricle
(future fourth ventricle)
Migrating vestibulocochlear ganglionic neurons originating in otic vesicle epithelium
Medial medullary NEP Medullary floor plate
Sequential waves of migrating medullary neurons
(midline raphe glial structure GEP)
Medial lemniscus
MEDULLA
Midline raphe glial structure
RHOMBENCEPHALON SPINAL CORD
Ventral funiculus
Spinal floor plate
(midline raphe glial structure GEP)
Spinal germinal zones
Ventral gray
Ventral NEP Intermediate gray Lateral funiculus
Intermediate NEP ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
central canal
Dorsal NEP Spinal roof plate
Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
PLATE 121A GW5 Coronal CR 8 mm C8314 Level 8: Section 172
Peripheral neural and non-neural structures labeled
Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing dura
Blood islands in developing pia
Cell-sparse Cell sparse superarachnoid reticulum Basilar artery Anterior cardinal vein Nerve V boundary cap (Schwann cell GEP?) Nerve V (trigeminal) Trigeminal ganglion (V) Nerve VII and VIII boundary caps (Schwann cell GEPs?) Anterior cardinal vein Vestibulocochlear ganglion (VIII)
Lumen
tem
Epithelium
por a l b o n e
Otic vesicle
us
260
Cell sparse superarachnoid reticulum
r Pe t
o
Nerve IX (glossopharyngeal)
Nerve and ganglion X (vagal)
Level 8: Computer-aided 3-D Brain Reconstruction
261
Central neural structures labeled
Brain surface (heavier line)
MESENCEPHALON
Superior collicular primordial plexiform layer
TECTUM
Mesencephalic roof plate
Tectal (superior collicular) NEP
PROPOSED RHOMBOMERE IDENTITIES
mesencephalic superventricle
R2
(future aqueduct)
TEGMENTUM
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
R3
Tegmental NEP Tegmental primordial plexiform layer
R4
Mesencephalic floor plate
(midline raphe glial structure GEP) Midline raphe glial structure Pioneer migrating tegmental neurons
PONS
PLATE 121B
R5
Midline raphe glial structure
R6
Pontine floor plate
(midline raphe glial structure GEP) Medial lemniscus? Migrating trigeminal neurons from R2 NEP Central trigeminal fibers
R7
R2 R3
Lateral pontine NEP
Migrating facial sensory neurons from R3 NEP
R4
rhombencephalic superventricle
(future fourth ventricle)
Lateral lemniscus?
Migrating vestibular and auditory neurons from R4+R5 NEPs
R5
Lateral medullary NEP
R6 R7?
Medial medullary NEP
Migrating solitary neurons (glossopharyngeal receptors) from R6 NEP
(hypoglossal [XII] and vagal [X] motor?)
MEDULLA
Migrating vagal sensory neurons from R7 NEP?
RHOMBENCEPHALON SPINAL CORD
Sprouting hypoglossal (XII) and vagal (X) nerve axons? Migrating medial medullary neurons
Ventral NEP
(merges with medial medullary NEP)
Spinal germinal zones
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Intermediate gray
Intermediate NEP
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating ventral spinal neurons
central canal
Dorsal NEP Spinal roof plate
Lateral funiculus Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
262
PLATE 122A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 9: Section 182
Blood islands in developing dura
Blood islands in developing pia
Primordial mesenchymal brain case (skin, bone, and meninges)
Cell-sparse Cell sparse superarachnoid reticulum
Anterior cardinal vein
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve V boundary cap
Nerve VII boundary cap? Nerve VIII boundary cap
Otic vesicle
l bo ne
Epithelium
mp
ora
Lumen
te
Schwann cell GEPs?
Nerve IX boundary cap
(Schwann cell GEP?)
Pe t r o
us
Nerve IX (glossopharyngeal) Nerve X (vagal)
Nerve XI (spinal accessory)
Level 9: Computer-aided 3-D Brain Reconstruction
263
PLATE 122B
Central neural structures labeled MESENCEPHALON
Brain surface (heavier line) Superior collicular primordial plexiform layer
TECTUM
Mesencephalic roof plate
PROPOSED RHOMBOMERE IDENTITIES
Tectal (superior collicular) NEP
R2
mesencephalic superventricle (future aqueduct)
TEGMENTUM/ISTHMUS
Tegmental NEP
R3 R4
Tegmental primordial plexiform layer Pioneer migrating tegmental neurons
isthmal canal
Isthmal primordial plexiform layer
R5
Pioneer migrating isthmal neurons Isthmal floor plate
R6
Isthmal NEP
(midline raphe glial structure GEP)
PONS
Midline raphe glial structure Medial lemniscus? Pontine floor plate
R7
(midline raphe glial structure GEP)
Medial pontine NEP
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Migrating trigeminal neurons from R2 NEP Central trigeminal fibers
R2 (trigeminal NEP) Clefts in NEP define rhombomere boundaries
R3 (facial sensory NEP)
Migrating facial sensory neurons from R3 NEP
rhombencephalic superventricle
R4 (vestibulo-auditory NEP)
Lateral lemniscus?
(future fourth ventricle)
R5 (vestibulo-auditory NEP)
Migrating vestibular and auditory neurons from R4+R5 NEPs
Clefts in NEP define rhombomere boundaries
R6 (glossopharyngeal NEP) R7? (vagal sensory NEP)
Solitary tract?
Migrating vagal sensory neurons from R7 NEP
Midlateral medullary NEP MEDULLA
(reticular formation?)
RHOMBENCEPHALON SPINAL CORD
Spinal germinal zones
Migrating solitary neurons (glossopharyngeal receptors) from R6 NEP
Migrating midlateral medullary neurons
Intermediate NEP
(merges with midlateral medullary NEP)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating intermediate spinal neurons Intermediate gray
Dorsal NEP
central canal
Spinal roof plate
Lateral funiculus Dorsal funiculus Dorsal gray
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
264
PLATE 123A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 10: Section 192
Blood islands in developing dura Blood islands in developing pia
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
Primordial mesenchymal brain case (skin, bone, and meninges)
Cell sparse Cell-sparse superarachnoid reticulum
Nerve V boundary cap
Nerve VII boundary cap? Nerve VIII boundary cap
Otic vesicle Epithelium
us
Lumen
t e mp o r a l b o n
e
t Pe Nerve IX boundary cap
ro
Schwann cell GEPs?
Nerve X boundary cap Schwann cell GEPs?
Level 10: Computer-aided 3-D Brain Reconstruction
265
PLATE 123B
Central neural structures labeled
Brain surface (heavier line) Superior collicular primordial plexiform layer
MESENCEPHALON TECTUM
PROPOSED RHOMBOMERE IDENTITIES
Mesencephalic roof plate
R2
Tectal (superior collicular) NEP
mesencephalic superventricle
R3
(future aqueduct)
Tectal (inferior collicular) NEP
R4
Inferior collicular primordial plexiform layer
R5
ISTHMUS
Isthmal primordial plexiform layer
Isthmal NEP
isthmal canal
Pioneer migrating isthmal neurons
R6
R7
RHOMBENCEPHALON PONS/CEREBELLUM
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Cerebellar NEP Pioneer cerebellar deep nuclear neurons Central trigeminal fibers
R2 (trigeminal NEP)
metencephalic pool Migrating trigeminal neurons from R2 NEP
Clefts in NEP define rhombomere boundaries
R3 (facial sensory NEP)
Migrating facial sensory neurons from R3 NEP
rhombencephalic superventricle
R4 (vestibulo-auditory NEP)
Lateral lemniscus?
(future fourth ventricle)
Migrating vestibular and auditory neurons from R4+R5 NEPs
R5 (vestibulo-auditory NEP)
R6 (glossopharyngeal NEP)
Clefts in NEP define rhombomere boundaries
Migrating solitary neurons (glossopharyngeal receptors) from R6 NEP
R7 (vagal sensory NEP)
Migrating vagal sensory neurons from R7 NEP
Midlateral medullary NEP (reticular formation?)
Posteromedial medullary NEP (merges with dorsal spinal NEP, gracile and cuneate?)
MEDULLA
Migrating cuneate nuclear neurons?
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
meyelencephalic pool
Migrating gracile nuclear neurons?
Medullary roof plate
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
266
PLATE 124A
Peripheral neural and non-neural structures labeled
GW5 Coronal CR 8 mm C8314 Level 11: Section 222 Blood islands in developing pia
Primordial mesenchymal brain case (skin, bone, and meninges)
Level 11: Computer-aided 3-D Brain Reconstruction
Blood islands in developing dura
267
PLATE 124B
Central neural structures labeled MESENCEPHALON TECTUM
Brain surface (heavier line)
Mesencephalic roof plate
mesencephalic superventricle (future aqueduct)
Tectal (inferior collicular) NEP Inferior collicular primordial plexiform layer
ISTHMUS
Isthmal NEP (trochlear?)
isthmal canal
Pioneer migrating isthmal (trochlear nucleus?) neurons
RHOMBENCEPHALON CEREBELLUM
Medial cerebellar NEP (vermis) Pioneer migrating cerebellar deep nuclear neurons
Lateral cerebellar NEP (hemisphere) Metencephalic roof plate (upper rhombic lip)
metencephalic pool
rhombencephalic superventricle (future fourth ventricle)
Lateral medullary velum
Myelenencephalic roof plate (lateral lower rhombic lip) Precerebellar NEP?
meyelencephalic pool
Pioneer migrating precerebellar neurons
Migrating cuneate nuclear neurons?
Posteromedial medullary NEP
(gracile and cuneate?)
Migrating gracile nuclear neurons?
MEDULLA ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medial medullary velum
Myelenencephalic roof plate (medial lower rhombic lip)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Arrows indicate the regionally shrinking shoreline of the superventricle as NEP cells are depleted while generating neurons.
268
PART PARTX: X: GW5 GW5 SAGITTAL SAGITTAL
Carnegie Collection specimen #8966 (designated here as C8966) with a 7.1 mm crown-rump length (CR) is estimated to be at gestational week (GW) 5. C8966 was preserved in Zenker’s fixative, embedded in a celloidin/ paraffin mix, and was cut in 10-µm sagittal sections that were stained with hematoxylin and eosin. Various orientations of the computer-aided 3-D reconstruction of C8314’s brain are used to show the gross external features of a GW5 brain (Figure 9). Like most sagittally cut specimens, C8966’s sections are not parallel to the midline; Figure 9 shows the approximate rotations in front (B) and back views (C). We photographed 29 sections at low magnification from the left to right sides of the brain. Seven of the sections, mainly from the left side of the brain, are illustrated in Plates 125AB to 131AB. Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify the approximate midline, non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (lowcontrast images) identify central neural structures. Plates 132AB to 133AB show high-magnification views of the rhombencephalon. The anterior part of the prosencephalic superventricle is tentatively identified as the future telencephalic superventricle, an enlargement of the diencephalic superventricle. The prosencephalic neuroepithelium is stockbuilding its various populations of neuronal and glial stem cells. The presumptive basal ganglionic and basal telencephalic neuroepithelia do not form mounds in the floor of the telencephalon. There is a definite lamina terminalis in the ventral prosencephalon that marks the site of closure of the anterior neuropore. The olfactory epithelium, in an anterolateral placode, is already producing nerve fibers.
The mesencephalon, arching between the mesencephalic and diencephalic flexures, is characterized by stockbuilding neuroepithelia surrounding an expanding mesencephalic superventricle. Cells have not yet migrated from the tectal and pretectal neuroepithelia. A few cells are migrating outside the tegmental and isthmal neuroepithelia. There is a very thin subpial fiber band. The rhombencephalon is the largest brain structure. Rhombomeres 2 through 7 form well-defined swellings in the lateral neuroepithelium. The rotation of C8966’s sections does not clearly show all the entry points of the cranial sensory nerves. However, rhombomere 2 is clearly associated with incoming axons from the trigeminal ganglion (V afferents), and rhombomeres 4 and 5 with the vestibulocochlear ganglion (VIII afferents). The association of rhombomere 3 with a tentatively identifiable facial ganglion (VII afferents) is less clear. Each rhombomere has a thin layer of pioneer migrating neurons, most are receptors for incoming sensory axons. However, there are many fewer fibers entering the brain from these ganglia than at GW5.5, and no fibrous swellings are in the very thin subpial fiber band. Sections near the midline show that rhombomeres do not extend into the medial pontine and medullary neuroepithelia. There is a thicker layer of migrating cells outside the medullary neuroepithelium, and the subpial fiber band is thicker as the brain blends with the spinal cord. The cerebellum stands out as the most immature and smallest rhombencephalic structure. In spite of that, a cerebellar notch can be identified laterally where the cerebellar and pontine neuroepithelia join. The most lateral sections cut the cerebellar neuroepithelium tangentially, allowing a few indistinct layers in the cerebellar transitional field to be identified.
269
EXTERNAL FEATURES OF THE GW5 BRAIN
th al
us
po
3
m
m
Hy
Upper rhombic lip
s
Future basal ganglia and basal telencephalon Preoptic area
Inferior colliculus
th
Choroid fissure
4
A perfect sagittal cut through the brain is parallel to the midline from anterior to posterior. Sections of C8966's brain rotate an estimated 13º clockwise from the midline, 6.5º to the right side of the anterior midline (B, front view), and 6.5º to the left side of the posterior midline (C, back view). In the sections illustrated on the following pages, anterior parts (top and left) are tilted away from the observer, while posterior parts (bottom and right) are tilted toward the observer.
Is
Eye
e
e re
PROSENCEPHALON
en gm tu
m
Future cerebral cortex
Superior colliculus
Pretectum
Thalamus
C
Side view
b e ll u
Epithalamus
Subthalamus a m us T
A.
n
Infundibulum Mammillary body
o
Rhombomere (R) 2 R3
P
2
R4
BRAINSTEM FLEXURES
Medullary velum
M
R5
1. Medullary
e
2. Pontine
R6
d
3. Mesencephalic
R7?
u
B.
Front view
1
a l l
Anterior midline
4. Diencephalic Lower rhombic lip
C.
Pretectum
Spinal cord
Epithalamus Thalamus
Pretectum
Back view
Superior colliculus
PROSENCEPHALON
Eye Choroid fissure
Eye
6.5º
e e b l l
e
r
Right side
C
m
R2 R3
Left side
R4
R5 R6 R7?
Medulla
Spinal cord Scale bars = 0.5 mm
Medullary velum
Left side
Figure 9. A, The lateral view of the left side of a computer-aided 3-D reconstruction of the brain and upper cervical spinal cord in C8314, the preceding GW5 specimen, which has a similar crown-rump length to C8966 (8 mm and 7.1 mm, respectively). External features are identified as in Figure 8B. The heavy numbered lines refer to brainstem flexures (boxed key). B, Front view of the brain in A. The angled line shows how C8966's sections rotate right (arrow) from the anterior midline. C, Back view of the brain in A. The angled line shows how C8966's sections rotate left (arrow) from the posterior midline.
Inferior colliculus
u
Isthmus Pons
Right side Rhombic lip border
Medulla
6.5º
Spinal cord
Posterior midline
270
PLATE 125A
GW5 Sagittal, CR 7.1 mm, C8966 Level 1: Slide 6 Section 2
Primordial mesenchymal brain case (skin, bone, and meninges)
mesencephalic superventricle
R
prosencephalic superventricle
IG
(future aqueduct)
H
thalamic pool
T
(future third ventricle)
Cell-sparse Cell sparse superarachnoid reticulum
subthalamic/ hypothalamic pool
isthmal canal
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Rathke's pouch epithedlium (primordium of anterior pituitary gland)
metencephalic pool
Arch III?
Arch IV?
rh om be n (f ce ut p ur h e f al ou ic rt s h up ve e nt r ri ve cl n e) tr ic le
Hyoid arch (II)
Bas ilar arte ry
Prim
o rd i
a of
Mandibular arch (I)
tong ue Or al ca vi ty
Cephalic placodes
myelencephalic pool
Medullary velum
S I D E
Cell-sparse Cell sparse superarachnoid reticulum
L E F T
Basal occipital bone?
O F
B R A I N
Pharynx
Medullary velum
M
I D
N E L I
DE
diencephalic superventricle
SI
(f
halice ncep l meserventriucct) e e aqued sup utur
(future lateral ventricles)
271
co
i
E DIENC
Pioneer migrating thalamic neurons
M
Epithalamic NEP
Posterior commissural GEP?
e
A tal) NEP
Inferior collicular
Brain surface (heavier line)
N L O
Superior collicular
(tec
E
P
Isthmal NEP
N
o
n
t
in
e
Migrating pontine (reticular formation?) neurons
Migrating trochlear (IV) neurons?
P
ic
P
lic
am H y p o t h al
E
NEP
Anterior
nc
e
l)
Middle
C
H
Mese
Pioneer migrating tegmental neurons
Posterior Preoptic NEP Lamina terminalis (site of anterior neuropore closure)
N
ha
cepha lic (tegm
E
p
en
Subthalamic NEP?
N
Labeled on this page: Central neural structures
S
ta
Basal telencephalic and septal NEP
E
P retectal N EP
ala mic NEP
es
Th
P
M
al
br Cere
rt
PLATE 125B
N LO HA
n
LO ON N((FFU PHAL UTT NCE UURR SE O EE TTE PPRR EL
N)) ON LLO HAA H P P E CE P NNC l NE ca LEE
Cerebellar NEP (vermis)
E
P
Pioneer migrating deep nuclear neurons Upper rhombic lip
M
id
li n e e
G EP ?
H
ph
R
ra
Midline raphe glial structure
O M
B
E N C
Upper
E P
H A
E P Migrating gracile and cuneate nuclear neurons?
Reticular, vagal motor, and hypoglossal NEP?
Gracile and cuneate nuclear NEP? Lower rhombic Lower lip
N
N
Ascending fiber tracts from spinal cord
O
Migrating hypoglossal (XII) and vagal motor (X) neurons?
L
M e d u l l a r y
Migrating medullary (reticular formation?) neurons
Nearly all parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. Medial parts of the medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
GW5 Sagittal, CR 7.1 mm, C8966 Level 2: Slide 5, Section 2
PLATE 126A Primordial mesenchymal brain case (skin, bone, and meninges)
M
thalamic pool
me s
(future lateral ventricles)
en
ce ut
L
I
N
ph e
ic
ur
aq
) ct
cle tri en rv
du
pe
ue
su
(future third ventricle)
D
al
(f
diencephalic superventricle
I
E
prosencephalic superventricle
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Branchial placodes
Inferior vagal ganglion (X)?
Cell-sparse Cell sparse superarachnoid reticulum myelencephalic pool
Sympathetic trunk ganglia? Nerve X boundary cap (Schwann cell GEP)? Nerve X (vagus)?
Medullary velum
O F
I D E S
T
Arch IV?
Medullary velum
L
E
F
ral late e r mo ely
of s ect ion shi fts pro gr ess iv
nx
ne
ary
P la
Ph
isthmal canal
rh om be n (f ce ut p ur h e f al ou ic rt s h up ve e nt r ri ve cl n e) tr ic le
ca vi ty ra l
Hyoid arch (II)
O
Arch III?
Rathke's pouch epithelium (primordium of anterior pituitary gland)
metencephalic pool
of ton gu e
Mandibular arch (I)
Cephalic placodes
Cell sparse Cell-sparse superarachnoid reticulum
B R A I N
subthalamic/ hypothalamic pool
Pr im or dia
272
See a higher magnification view of the entire rhombencephalon, parts of the mesencephalon, and diencephalon in Plates 132A and B.
273
r
co al
rti
c
D I E NC
P T h a l a mic NE
Pre
Epithalamic NEP
Ce
re
b
HALON) CEP N E NEP EL al
tec M ta E l N Posterior S EP commissural E GEP? N
C E
P P
M Brain surface (heavier line)
NE P
Migrating trigeminal nuclear complex (V) neurons from R2 NEP Migrating facial (VII) neurons from R3 NEP
Isthmal (trochlear nuclear) NEP?
Cerebellar NEP (vermis)
R2
R3
O N
Inferior collicular
P
N E
Isth ma l
Middle H y p o t i c h a l a m
alic (tectal) N E
Anterior
ph
Posterior
L
ce Superior collicular
al) NEP nt
Lamina terminalis (site of anterior neuropore closure)
en
ephalic (tegm enc e es
Preoptic NEP
A
es
Basal telencephalic and septal NEP
Labeled on this page: Central neural structures
H
M
NCEPHALO OSE N( PR FU
TU RE
T
PLATE 126B
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals R - Rhombomere Germinal zone - Helvetica bold Transient structure - Times bold italic ON L A Permanent structure - Times Roman or Bold EPH
Pontine NEP Upper rhombic lip
R4 Migrating vestibular and auditory neurons from R4+R5 NEPs
R
H
O
U pper
R5
M
B
E
Medullary NEP
PROPOSED RHOMBOMERE IDENTITIES
N
R6
C
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
E
R2
P
L
er
R3 R4
O
R7
Lower rhombic lip
A
Lo w
H
Migrating vagal sensory (X) neurons from R7 NEP
N R5
Nearly all parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. Medial parts of the medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
R6 Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
274
PLATE 127A
GW5 Sagittal, CR 7.1 mm, C8966 Level 3: Slide 4, Section 7 ENTIRE SECTION I S FR O
Primordial mesenchymal brain case (skin, bone, and meninges)
prosencephalic superventricle
M L E
FT
DE
me s
thalamic pool
(future lateral ventricles)
SI
OF
en
ce ut
e
ic
aq
) ct
cle tri en rv
du
pe
ue
su
(future third ventricle)
N
ph
ur
diencephalic superventricle
AI
al
(f
BR
subthalamic/ hypothalamic pool
Maxillary process?
Cell-sparse Cell sparse superarachnoid reticulum
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
Cephalic placodes Cell-dense Cell dense mesenchyme
Nerve IX boundary cap (Schwann cell GEP)?
Nerve X (vagus)
Superior vagal ganglion (X)?
eo
fs
Nerve IX (glossopharyngeal)
Inferior vagal ganglion (X)?
h if
Medullary velum
ns
Lumen
Epithelium
ts p
rhombencephalic superventricle
(future fourth ventricle)
tio
Otic vesicle
rog ress ivel y
Vestibulocochlear ganglion (VIII)
r
Arch III Inferior glossopharyngeal ganglion (IX)
m or e lat
c
a
metencephalic pool
ec
O
eral
v
of ton gu e
a l
Branchial placodes
Pr im or dia
Hyoid arch (II)
i t y
Mandibular arch (I)
myelencephalic pool
Pl
an
275
D IEN C E
o
Thala
bra
lc
ON) HAL EP C P EN l N E EL r t i c a
PLATE 127B
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
ON AL H P
NE mic
Pre
P
Epithalamic NEP
M tec
Posterior commissural GEP?
E
tal
S
NE
E
N
P
C
E
P
H A
L
Basal telencephalic and medial basal ganglionic NEP
M
N lic (tec
NE
Brain surface (heavier line)
tal )
Inferior collicular
P
Migrating isthmal neurons
Migrating hypothalamic neurons
Sprouting nerve IV (trochlear)?
Isthmal NEP
R2
Migrating facial sensory (VII) neurons from R3 NEP
R3
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium? epithelium?
EP ar N bell ere) Cer(heemisph
Migrating trigeminal nuclear complex (V) neurons from fromR2 R2NEP? NEP
Peripheral neural structure
pha
Labeled on this page: Central neural structures
Migrating subthalamic Migrating tegmental neurons? neurons
Middle/ EP lateral i c N am al th
Superior collicular
ce
Posterior
Anterior H ypo
en
anterior neuropore closure) Pioneer migrating basal telencephalic and basal ganglionic neurons
O
es
Mesencephali c( t
Subthalamic NEP? Lamina terminalis (site of
Preoptic NEP
EP ntal) N me eg
ALON (FU CEPH TU SEN RE O Cere PR T
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medial cerebellar notch?
Pontine NEP
R H
R4
Pioneer migrating deep nuclear neurons?
O
Upper rhombic lip
M
B
A
L
O
N
R6
H
R5
P
R4
E
R3
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
Lower rhombic lip
C
R2
R6
Medullary NEP
N
PROPOSED RHOMBOMERE IDENTITIES
R5
E
Migrating vestibular and auditory neurons from R4+R5 NEPs
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
Nearly all parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase. Medial parts of the medullary NEP form shrinking shorelines of the superventricle as stockbuilding NEP cells decrease.
276
PLATE 128A
GW5 Sagittal, CR 7.1 mm, C8966 Level 4: Slide 3, Section 24 ENTIRE
Primordial mesenchymal brain case (skin, bone, and meninges)
SECTI
ON I S FR O
M L EFT SID E
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular OF divisions BR
prosencephalic superventricle
me s
(future lateral ventricles)
thalamic pool
en
ce ut
ph e
ic
ur
aq
) ct
cle tri en rv
Otic vesicle
eral gre
ssiv ely
Branchial placode
fts
shi Medullary velum
Epithelium Lumen
Otic canal (marks the initial invagination of the otic placode)
Nerve VII (facial) Nerve VIII (vestibulocochlear)
See a higher magnification view of the rhombencephalon from this section in Plates 133A and B.
e ct
io n
rhombencephalic superventricle
(future fourth ventricle)
of s
ganglion (VIII)
metencephalic pool
ne
O Vestibulocochlear
Pla
Facial ganglion (VII)?
pro
Nerve VII and VIII boundary caps (Schwann cell GEPs)? Nerves VII and VIII
r
a l
c
a
Pr im or dia
of ton gu e
v i t y
Cell dense Cell-dense mesenchyme
Cell-sparse Cell sparse superarachnoid reticulum
m or e lat
Placodal epithelium (maxillary)
Arch III?
du
optic recess
Maxillary process
Hyoid arch (II)
pe
ue
l
/ ic oo m p la m ic a h a bt al su oth p hy
Mandibular arch (I)
su
(future third ventricle)
IN
al
(f
diencephalic superventricle
A
277 FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 128B
Arrows indicate the presumed direction of neuron migration from germinal sources.
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Labeled on this page: Central neural ALON) structures EPH NC
DI ha
T
E NC
H EP
l a mic N
AL
EP
ON Pretecta l
Epithalamic NEP
I st
h
m
NE P ic
Migrating isthmal neurons?
R3
CTF2 (deep nuclear neurons) CTF3 (deep nuclear neurons and fibers)
EP r Nre) lla he be isp re em Ce (h
R2
RH OM
Pontine NEP
Upper rhombic lip Lower rhombic lip
B
R4
al N P? E
CTF1 (fibers)
Medial cerebellar notch
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
N L O
Inferior collicular
A
Superior collicular
Brain surface (heavier line)
Migrating subthalamic neurons?
Migrating hypothalamic neurons
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium
H
ic
m la ha Hypot
Migrating facial sensory (VII) neurons from R3 NEP
E ) NEP P ectal c (t E ali ph C ce en es
am
Preoptic NEP
Peripheral neural structure
S
M
t h al
Mesencepha lic (teg m Migrating tegmental neurons
P NE
NEP tal) en
S ub
Optic nerve (II) GEP?
E
Posterior commissural GEP?
Basal telencephalic and lateral basal ganglionic NEP
Pioneer migrating basal telencephalic and basal ganglionic neurons
M
NEP ?
N
ALON (FU NCEPH TU OSE RE PR e b ral Cer co r
LE l NEP ca TE ti
E N C
P
H
A
L
ON
from R4 NEP?
E
Migrating auditory Migrating vestibular and auditory (VIII)R4 neurons (VIII) neurons from NEP
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
All parts of the NEP in this section form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
278
PLATE 129A
GW5 Sagittal, CR 7.1 mm, C8966 Level 5: Slide 3, Section 12
ENTIRE SECTIO N
IS FR O
M L E
FT
Primordial mesenchymal brain case (skin, bone, and meninges)
prosencephalic superventricle
SID
E
OF
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
BR
AI
N
mes supeencepha lic (futu rvent re aq ricl e ue
(future lateral ventricles)
duct )
Nerve I (olfactory) Olfactory placode Maxillary process
Cell sparse superarachnoid reticulum
Placodal epithelium (maxillary)
eral
Sphenoid bone?
optic recess
Facialganglion ganglion Facial (VII)placode? placode? (VII)
m or e lat rog res sive ly
ts p h if
ns tio sec
Facial ganglion (VII)? Nerve VII? Nerve VIII
of
al Orvity a c
Hyoid arch (II)
ne
Branchial placodes
Nerve V boundary cap (Schwann cell GEP)?
P la
Mandibular arch (I)
Ant erio r ca rdin al v ein?
Cell dense mesenchyme
Vestibulocochlear ganglion (VIII) Petrous temporal bone
Otic vesicle Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear)
Epithelium
rhombencephalic superventricle
Lumen
(future fourth ventricle, metencephalic pool)
Medullary velum
279 FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 129B
Arrows indicate the presumed direction of neuron migration from germinal sources.
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Labeled on this page: Central neural structures
am
M N
E
Posterior commissural GEP?
P
C
ic NEP
E
N
al
e ctal
Me sen ceph alic (t egme ntal )N E Migrating tegmental neurons Migrating subthalamic Brain surface neurons? (heavier line)
P
h
Pret
Epithalamic NEP
E
T
Migrating thalamic neurons
S
Cerebra
l
c
DIENCEPHALON
al N E P
PROSENCEPHALON (FUTURE TELENCEPHALON)
tic or
E P
H
en
P
NE l)
a l ic
N L O
ph (tecta
Migrating hypothalamic neurons
A
ce
Pioneer migrating basal telencephalic and basal ganglionic neurons
Hypothalamic and preoptic NEPs
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Cer e (he be mi lla
sp he re
Cochlear nucleus nuclear NEP?
RH OM
Pontine NEP
EP rN ) Upper rhombic lip
B
E
Lower rhombic lip
C E
A
L
Migrating cochlear nuclear neurons?
N
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium
Migrating facial sensory (VII) neurons from R3 NEP?
R2
R 3?
Migrating facial ganglionic (VII) neurons from germinal source in pacode?
Central trigeminal fibers
CTF2+3 (deep nuclear neurons and fibers)
H
Peripheral neural structures
Medial cerebellar notch CTF1 (fibers)
P
Optic nerve (II) GEP?
es
P
Basal telencephalic and lateral basal ganglionic NEP
NE
M
Su
ami c bthal
ON PROPOSED RHOMBOMERE IDENTITIES R2 R3
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion.
All parts of the NEP in this section form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
280
PLATE 130A
GW5 Sagittal, CR 7.1 mm, C8966 Level 6: Slide 3, Section 5
Primordial mesenchymal brain case (skin, bone, and meninges)
ENTIRE
SECTI
prosencephalic superventricle
ON IS FROM
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions LEF
T S IDE
(future lateral ventricles)
OF
BR
A
IN
Nerve I (olfactory)
Olfactory placode
EYE
optic recess
Cell-sparse Cell sparse superarachnoid reticulum
Placodal epithelium (maxillary) Sphenoid bone? ior ter An
ter a
Trigeminal ganglion (V)
re l a
Mandibular arch (I)
l
? ein lv ina rd ca
Cell-dense Cell dense mesenchyme
mo
Maxillary process
pro
gre
ssiv ely
Nerve V boundary cap (Schwann cell GEP)?
ion
ect fs
eo
Vestibulocochlear ganglion (VIII)
an
Facial ganglion (VII) placode?
Pl
Ant erio r ca rdin al v ein?
shi
fts
Facial ganglion (VII)
Hyoid arch (II)
Petrous temporal bone
Nerve V (trigeminal)
Otic vesicle
Epithelium
Lumen
281
PLATE 130B Labeled on this page: Central neural structures PROSENCEPHALON (FUTURE TELENCEPHALON)
Cerebral cortical NEP MESENCEPHALON Basal telencephalic and lateral basal ganglionic NEP
Brain surface (heavier line)
Pretectal NEP Posterior commissure GEP?
Opthalmic germinal zones
Migrating Pioneer migrating basal Subthalamic subthalamic neurons? telencephalic and basal NEP ganglionic neurons
Pigment epithelium germinal zone
Migrating pretectal and tectal neurons?
Mesencephalic (tectal) NEP
DIENCEPHALON
Retinal NEP Optic nerve (II) GEP?
Peripheral neural structure
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Migrating facial ganglionic (VII) neurons from germinal source in pacode
Central trigeminal fibers
Pontine NEP R2 RHOMBENCEPHALON
All parts of the NEP in this section form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
PROPOSED RHOMBOMERE IDENTITIES IDENTITY PROPOSED RHOMBOMERE R2
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
282
PLATE 131A
Primordial mesenchymal brain case (skin, bone, and meninges)
GW5 Sagittal, CR 7.1 mm, C8966 Level 7: Slide 2, Section 22
ENTIRE SECT IO
prosencephalic superventricle
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions N IS FR OM LEFT
SIDE
BR
A
IN
(future lateral ventricles)
OF
Cell dense mesenchyme
Cell-sparse Cell sparse superarachnoid reticulum
EYE
gress ively m or
Olfactory placode
e later al
Sprouting Nerve I (olfactory) axons
Pigment epithelium Intraretinal space Retinal NEP
Mandibular arch (I)
An ter ior
Facial ganglion (VII) placode?
car din al
vei n?
Trigeminal ganglion (V)
tio n
f sec ne o
Trigeminsl ganglion (V) placode?
Pla
An ter ior ca rd in al ve in ?
Maxillary process
s h ift
Sphenoid bone?
Placodal epithelium (maxillary)
Hyoid arch (II)
s pro
Choroid fissure
283
PLATE 131B Labeled on this page: Central neural structures
PROSENCEPHALON (FUTURE TELENCEPHALON)
MESENCEPHALON
Mesencephalic (tectal) NEP
Cerebral cortical NEP
Basal telencephalic and lateral basal ganglionic NEP?
Brain surface (heavier line)
Migrating tectal neurons
Peripheral neural structures structures originoriginating from the ating from central nervous central nervous system: system: Opthalmic germinal zones Pigment epithelium germinal zone Retinal NEP Optic nerve (II) GEP?
All parts of the NEP in this section form expanding shorelines of the superventricles as stockbuilding NEP cells increase. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from germinal sources.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
See Level 2 in Plates 126A and B.
HYPOTHALAMUS, MESENCEPHALON, AND RHOMBENCEPHALON PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4 R5 R6 R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
284
PLATE 132A GW5 Sagittal, CR 7.1 mm, C8966 Level 2: Slide 5, Section 2
PLATE 132B
Cerebellar NEP
Upper rhombic lip
(vermis)
Mesencephalic (tectal, inferior collicular) NEP
ABBREVIATIONS: FONT KEY: NEP - Neuroepithelium ventricular divisions - capitals R - Rhombomere Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Medullary velum
tectal pool
Trochlear nuclear NEP?
metencephalic pool
isthmal canal
mesencephalic superventricle
Lower rhombic lip
Reticular NEP?
Cell-sparse superarachnoid reticulum
Migrating pontine reticular formation neurons?
EP
la
(future third ventricle)
Trigeminal NEP
Facial R3? sensory NEP
Medullary NEP Upper
R4
Vestibuloauditory NEP
R5
Vestibuloauditory NEP
Migrating facial sensory (VII) neurons
a t h o p H y
diencephalic superventricle
R2
Migrating trigeminal nuclear complex (V) neurons
ic
Me se
Posterior (mammillary)
Pontine NEP
Middle
hypothalamic pool
Rathke's pouch epithelium (primordium of anterior pituitary gland) Oral cavity
myelencephalic pool
Migrating vestibular and auditory (VIII) neurons
R6
Glossopharyngeal NEP
Lo we r
(future fourth ventricle)
Isthmal NE P
m
ic (tegme hal nt p e c n
EP )N al
rhombencephalic superventricle
N
tegmental pool
(future aqueduct)
R7 Vagal sensory NEP
Migrating vagal sensory (X) neurons Migrating solitary nuclear neurons (IX glossopharyngeal receptors)
Nerve X Nerve X boundary (vagus)? cap (Schwann cell GEP?)
Sympathetic trunk ganglia?
Oral cavity
Primordia of tongue Mandibular arch (I)
Hyoid Pharynx arch (II)
285
CEREBELLUM AND PONS
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
See Level 4 in Plates 128A and B.
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
GW5 Sagittal, CR 7.1 mm, C8966 Level 4: Slide 3, Section 24
286
PLATE 133A
PLATE 133B
Otic vesicle
(future fourth ventricle) metencephalic pool
*Note that incoming afferent axons do not form a characteristic "bulge" at the brain surface as in the other GW5 specimen (C8314). That indicates C8966 is less mature than C8314, and massive fiber ingrowth occurs during GW5.
Cerebellar NEP (hemisphere)
Migrating vestibular and auditory (VIII) neurons from R4 NEP
R4
vestibuloauditory NEP
Nerve VIII boundary cap
Pioneer VII and VIII afferent axons enter brain*
Nerve VIII (vestibulocochlear) Schwann cells plentiful Schwann cells scarce
Pontine NEP
R3
Cerebellar notch
CTF3 (deep nuclear neurons and fibers)
facial sensory NEP
Schwann cells migrate into peripheral nerve from GEP in boundary cap?
R2
Brain surface (heavier line)
Cell-sparse superarachnoid reticulum
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Nerve VII boundary cap
Ep ith eli um
Lumen
Vestibulocochlear ganglion (VIII)
trigeminal NEP
CTF2 (deep nuclear neurons) CTF1 (fibers)
tion l ina ana ag ) c c inv de Oti itial laco e in ic p s th ot ark the (m of
Lower rhombic lip
rhombencephalic superventricle
Migrating facial sensory (VII) neurons from R3 NEP Migrating trigeminal nuclear complex (V) neurons from R2 NEP
ABBREVIATIONS: CTF - Cerebellar transitional field GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Nerve VII (facial, full of Schwann cells) Facial ganglion (VII)?
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium
Arrows indicate the presumed direction of neuron and glia migration from germinal sources.
287
288
PART PARTXI: XI: GW4.5 GW4.5 CORONAL CORONAL
This specimen is embryo #2300 in the Minot Collection, designated here as M2300. The crown-rump length (CR) is 6.3 mm estimated to be at gestational week (GW) 4.5. M2300’s prosencephalic and anterior mesencephalic sections are cut (8 µm) in the coronal plane, but the plane shifts to predominantly horizontal in the posterior mesencephalon, pons, and medulla. We photographed 48 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and medulla. Fourteen of these sections are illustrated in Plates 134AB to 146AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of M2300’s brain and optic vesicle (Figure 10), and to show each illustrated section in situ (insets, Plates 134A to 146A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. The prosencephalon is considerably smaller than at GW5 (Part IX) with a stockbuilding neuroepithelium surrounding a small prosencephalic superventricle. Anterior sections are tentatively identified as the future telencephalon, while sections of the optic vesicle and posterior to it are more clearly identified as diencephalic. Cell migration is absent in both future telencephalic and diencephalic parts of the prosencephalon. The olfactory placode forms a thick epithelium in the anterolateral surface of the head that is much closer to the brain than at GW5. There is a thinner epithelium connecting the olfactory placode and the lens placode. The evaginated optic vesicle is just beginning to curve around the lens placode. However, a definite inner retinal neuroepithelium (thick with presumptive glial chan-
nels adjacent to the lens) and an outer pigment epithelium (thin) can be differentiated. The mesencephalon contains a stockbuilding neuroepithelium in the pretectum and tectum; cell migration has not yet begun. The tegmental and isthmal neuroepithelia, thicker than at GW5, are stockbuilding their stem cell populations. Only a few pioneer neurons have migrated out, perhaps these are sequestered in the outer parts of the neuroepithelium itself rather than outside it. The subpial fiber band is very thin in the tegmentum, but thickens slightly in the isthmus. The most prominent neuroepithelial structures in the rhombencephalon are the rhombomeric evaginations. In this specimen, several sections show how closely rhombomeres are associated with sensory cranial ganglia. The trigeminal ganglion (source of V sensory axons) is nearly attached to the brain surface at rhombomere 2. The vestibulocochlear ganglion (source of VIII axons) is attached to the rhombomere 4 brain surface. The otic vesicle touches the rhombomere 5 brain surface. The short nerve extending from the large vagal ganglion (source of X sensory axons) touches the rhombomere 7 brain surface. The subpial fiber band is thin throughout the rhombencephalon; even though sensory axons are touching the brain, they have yet to enter it. A very thin layer of migrating neurons lines the superficial border of some rhombomeres; for the most part, cell migration has not yet started. The small stockbuilding cerebellar neuroepithelium is only identifiable in the most posterior sections of the rhombencephalon. There are no migrating neurons outside the cerebellar neuroepithelium, only a thin cell-free fibrous layer.
289
M2300 Computer-aided 3-D Brain Reconstructions A. B. s
H
me du l
th ala m
po
P
ll R7
1. Medullary
we
P R O
S
la
a ull ed rm
3. Mesencephalic
1
4. Diencephalic
Ventral rhombic lip
Spinal cord
Spinal cord
Optic vesicle
R2
Figure 10. A, The left side of the 3–D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
P
n
Optic vesicle
P
s
Futu r e b a s
R6
R7
la
in a l
C o
med u
l
R5
er
r medu ll pe
U
p
a
ow
s o
P
n s o
t h a l a
m
n
u s
a r e a
m e g m e n t u m u s h I s t
P
al
T
ce
o
en
H y p
F
b asal tel
P r e o p t i c
ut u re sept u m ph ng li a a l o n
ture
R4
r
R3
ga
N C E P H A S E L O O R
Scale bars = 0.5 mm
Upper rhombic lip
R2
N
Fu
m u s C e r e b e l l u m
Su
h
In
fer
perior colliculu
ior colliculu
s
s
r e t e c t u m
s
t h a l a m p i u E
a l a m u T h s
re telencephalo n Futu
R P
Bottom view
o
t
s
L
O
I P
D.
Medullary velum
N C E P H A L S E O
N
Top view
d
C.
Medullary velum
Lo
Low er
R6
a
BRAINSTEM FLEXURES
R7
R5
ed u
R6
e d u ll a
R3 R4
Infundibulum Mammillary body
Dorsal rhombic lip
R2
per m Up
Up
rm
3
o n s
Sub th al Te
O
R
s n
N O
S u bthal am Hy pothalam us us T
o
R4 R5
pe
Preoptic area
Rhombomeres
R3
P
Hy
P
E P H A N C L
Optic vesicle
m llu
s
Pr eoptic area
gme
4
Future telencephalon
R2
Inferior colliculus
s hmu Ist
h mu
Optic vesicle
E
Epithalamu s lamus u Tha am
e reb Ce
m en
L
Superior colliculus
N
O
um nt
us t e l F uture e n c ep h alo n
eg
llum e be Ce r
Thal am
Pretectum
A
Inferior colliculus
tu m I s t
s mu
Epithala
Side view
S E N C E P
Pretectum
us
Superior colliculus
Angled front view
S
p
290
PLATE 134A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300
Level 1: Section 5 Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing meninges
Olfactory placode
Level 1: Computer-aided 3-D Brain Reconstruction
Level 2: Section 35
Primordial mesenchymal brain case (skin, bone, and meninges)
Blood islands in developing meninges Frontonasal process?
Olfactory placode
Mesenchymal densities between placode and future central olfactory structures
Level 2: Computer-aided 3-D Brain Reconstruction
Preplacodal epithelium
291
PLATE 134B
Central neural structures labeled
Level 1: Section 5 ANTERIOR PROSENCEPHALON
Brain surface (heavier line)
Prosencephalic roof plate
Prosencephalic primordial plexiform layer
prosencephalic superventricle
Prosencephalic NEP (future telencephalic)
(future lateral and third ventricles)
Prosencephalic floor plate
Level 2: Section 35 PROSENCEPHALON Prosencephalic roof plate
Brain surface (heavier line)
Prosencephalic NEP (future thalamic)
Prosencephalic NEP (future telencephalic)
prosencephalic superventricle
Prosencephalic primordial plexiform layer
(future lateral and third ventricles)
Prosencephalic NEP
(future preoptic/hypothalamic)
Prosencephalic floor plate
NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
292
PLATE 135A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 3: Section 65
Primordial mesenchymal brain case (skin, bone, and meninges) Dense mesenchyme between optic vesicle and brain
OPTIC VESICLE Pigment epithelium Intraretinal space Retinal NEP Lens placode
Future oral cavity
Preplacodal epithelium
Mandibular arch (I)
Lateral tongue primordia Part of the mandibular arch placodal epithelium gives rise to the thyroid gland.
The GW4 Face and Neck
Figure 247A modified (Patten, 1953, p. 429.)
Frontal prominence Optic vesicle Olfactory placode Future oral cavity Tongue and mandible primordia
Maxillary process Mandibular arch (I)
Hyo-mandibular cleft Hyoid arch (II) Arches III and IV
Level 3: Computer-aided 3-D Brain Reconstruction
293
PLATE 135B
Central neural structures labeled
DIENCEPHALON THALAMUS
Diencephalic roof plate
(future choroid plexus in roof of third ventricle)
Brain surface (heavier line)
Thalamic NEP
Thalamic primordial plexiform layer
SUBTHALAMUS
Subthalamic NEP Preoptic area NEP
Subthalamic primordial plexiform layer Preoptic area primordial plexiform layer
diencephalic superventricle (future third ventricle)
optic recess
Anterior hypothalamic NEP Diencephalic floor plate (future chiasmal GEP)
Glial channels in retinal NEP?
Hypothalamic primordial plexiform layer Chiasmal glial channels?
PREOPTIC AREA/ HYPOTHALAMUS
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
294
PLATE 136A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 4: Section 75
Primordial mesenchymal brain case (skin, bone, and meninges)
Dense mesenchyme between optic vesicle and brain
OPTIC VESICLE Pigment epithelium Intraretinal space Retinal NEP Lens placode
Maxillary process Future oral cavity
Preplacodal epithelium Lingual epithelium Lateral tongue primordia
Mandibular arch (I)
Arterial trunk
Hyoid arch (II)
Level 4: Computer-aided 3-D Brain Reconstruction
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
295
PLATE 136B
Central neural structures labeled DIENCEPHALON THALAMUS/EPITHALAMUS
Diencephalic roof plate
(future pineal gland?) Brain surface (heavier line)
Thalamic/epithalamic NEP
SUBTHALAMUS
Subthalamic NEP
Glial channels in retinal NEP?
pineal recess?
Thalamic/epithalamic primordial plexiform layer
diencephalic superventricle (future third ventricle)
Subthalamic primordial plexiform layer
optic recess
Anterior hypothalamic NEP Diencephalic floor plate (future chiasmal GEP)
Hypothalamic primordial plexiform layer Chiasmal glial channels?
PREOPTIC AREA/ HYPOTHALAMUS
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
296
PLATE 137A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 5: Section 85 Formative superarachnoid reticulum (cell sparse)
Primordial mesenchymal brain case (skin, bone, and meninges)
Sphenoid primordium?
OPTIC VESICLE
Pigment epithelium Intraretinal space Retinal NEP
Maxillary process Rathke's pouch epithelium (primordium of adenohypophysis) Future oral cavity
Preplacodal epithelium Lingual epithelium Lateral tongue primordia
Mandibular arch (I)
Medial tongue primordia
Hyoid arch (II)
Arch III
Arterial trunk
Arch IV?
Laryngo-tracheal groove
Level 5: Computer-aided 3-D Brain Reconstruction
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
297
PLATE 137B
Central neural structures labeled DIENCEPHALON THALAMUS/EPITHALAMUS
Diencephalic roof plate
Brain surface (heavier line)
(future pineal gland?)
Thalamic/epithalamic NEP SUBTHALAMUS
Subthalamic NEP
optic recess
pineal recess?
diencephalic superventricle
Thalamic/epithalamic primordial plexiform layer
(future third ventricle)
Subthalamic primordial plexiform layer
Hypothalamic primordial plexiform layer infundibular recess
Middle hypothalamic NEP Diencephalic floor plate
(future median eminence and neurohypophyseal GEP)
HYPOTHALAMUS
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
298 Peripheral neural and non-neural structures labeled
PLATE 138A GW4.5 Coronal CR 6.3 mm M2300 Level 6: Section 95
Formative superarachnoid reticulum (cell sparse)
Primordial mesenchymal brain case (skin, bone, and meninges)
Anterior cardinal vein
d oi ? en dium h Sp mor i pr
Rathke's pouch epithelium (primordium of adenohypophysis)
Maxillary process
Future oral cavity Preplacodal epithelium Lingual epithelium
Mandibular arch (I)
Lateral tongue primordia Medial tongue primordia
Hyoid arch (II)
Laryngo-tracheal groove
Arch III Arch IV?
Ph
ary
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
nx Vagal ganglion (X) placode? Vagal ganglion (X)
Dorsal aorta
Notochord
Level 6: Computer-aided 3-D Brain Reconstruction
299 Central neural structures labeled MESENCEPHALON
Pretectal/tectal primordial plexiform layer
PRETECTUM/TECTUM
Mesencephalic roof plate
(posterior commissural GEP?)
Pretectal/tectal NEP
PLATE 138B
Pioneer posterior commissure fibers
mesencephalic superventricle
Brain surface (heavier line)
(future aqueduct)
TEGMENTUM
Tegmental NEP
Tegmental primordial plexiform layer First tegmental neuronal migration Hypothalamic primordial plexiform layer
Posterior hypothalamic (mammillary) NEP
mammillary recess
Diencephalic floor plate HYPOTHALAMUS
DIENCEPHALON
Peripheral neural structure Migrating vagal ganglionic neurons from germinal source in vagal placode?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
300
PLATE 139A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 7: Section 115 Primordial mesenchymal brain case (skin, bone, and meninges)
Anterior cardinal vein
Cell-sparse formative superarachnoid reticulum
id ? no m he iu Sp ord im pr
Fused maxillary process and mandibular arch (I)
Notochord
Trigeminal ganglion (V) placode?
Future oral cavity Lingual epithelium Medial tongue primordia
Hyoid arch (II)
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Arch III
Vagal ganglion (X) placode?
Arch IV
Facial ganglion (VII) placode?
Arytenoid swelling
Glottis Larynx
Vagal ganglion (X)
Pharynx
Dorsal aorta Sympathetic trunk?
Notochord
Dorsal root ganglion Dermatome
Level 7: Computer-aided 3-D Brain Reconstruction
Dorsal root of spinal nerve
301
Central neural structures labeled
Brain surface (heavier line)
TECTUM
Mesencephalic roof plate
mesencephalic superventricle
Tectal NEP
PLATE 139B
Tectal primordial plexiform layer
(future aqueduct)
TEGMENTUM Tegmental primordial plexiform layer
Tegmental NEP Mesencephalic floor plate
Medial lemniscus?
(midline raphe glial structure GEP?)
Midline raphe glial structure
MESENCEPHALON
Peripheral neural structures Migrating trigeminal ganglionic neurons from germinal source in trigeminal placode?
Migrating vagal ganglionic neurons from germinal source in vagal placode?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
SPINAL CORD Ventral funiculus Ventral gray Lateral funiculus
FONT KEY: ventricular divisions - capitals central canal Germinal zone - Helvetica bold Transient structure - Times bold italic Dorsal Permanent structure - Times Roman or Bold funiculus
Spinal floor plate
(ventral commissural GEP)
Ventral NEP
Intermediate NEP Dorsal NEP Spinal roof plate
Spinal germinal zones
302
PLATE 140A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 8: Section 135 Primordial mesenchymal brain case (skin, bone, and meninges)
Fused maxillary process and mandibular arch (I) Anterior cardinal vein
Trigeminal ganglion (V)
Trigeminal ganglion (V) placode?
Facial ganglion (VII)?
Hyoid arch (II)
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Cell-sparse formative superarachnoid reticulum Arch III
Vagal ganglion (X) placode?
Facial ganglion (VII) placode? Glossopharyngeal ganglion (IX)?
Glossopharyngeal ganglion (IX) placode?
Notochord
Vagal ganglion (X) Dorsal aorta Sympathetic trunk?
Notochord
Dorsal root ganglion
Dorsal root of spinal nerve
Level 8: Computer-aided 3-D Brain Reconstruction
Dermatome
303 Central neural structures labeled
Brain surface (heavier line)
MESENCEPHALON
Tectal primordial plexiform layer
TECTUM
Mesencephalic roof plate Tectal NEP
mesencephalic superventricle (future aqueduct)
isthmal canal
TEGMENTUM/ISTHMUS
Tegmental/isthmal NEP
Tegmental/isthmal primordial plexiform layer Migrating isthmal neurons Migrating central trigeminal neurons
rhombencephalic superventricle
PONS
PLATE 140B
R2 (trigeminal NEP)
Presumptive migrating ganglionic neurons from germinal sources in branchial placodes?
(future fourth ventricle)
Trigeminal ganglionic neurons
Medial pontine + R3 NEP
(abducens [VI], facial motor [VII]?)
Migrating abducens (VI) and facial motor (VII) neurons?
MEDULLA
Facial ganglionic neurons
Medial medullary NEP Migrating medial medullary neurons
Medullary floor plate
(midline raphe glial structure GEP?)
Glossopharyngeal ganglionic neurons Vagal ganglionic neurons
Lower medullary NEP? RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
PROPOSED RHOMBOMERE IDENTITIES R2
R3
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion.
SPINAL CORD Spinal floor plate Ventral funiculus Ventral gray
ABBREVIATIONS: Lateral GEP - Glioepithelium funiculus NEP - Neuroepithelium R - Rhombomere central FONT KEY: canal ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Dorsal Permanent structure - Times Roman or Bold funiculus
(ventral commissural GEP)
Ventral NEP
Intermediate NEP Dorsal NEP Spinal roof plate
Spinal germinal zones
304
PLATE 141A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 9: Section 145 Primordial mesenchymal brain case (skin, bone, and meninges)
Trigeminal boundary cap (Schwann cell GEP?)
Fused maxillary process and mandibular arch (I)
Trigeminal ganglion (V)
Vestibulocochlear ganglion (VIII)?
Facial ganglion (VII) placode?
Facial ganglion (VII)? Hyoid arch (II)
Otic vesicle epithelium
Glossopharyngeal ganglion (IX) Glossopharyngeal ganglion (IX) placode?
Vagal ganglion (X)
Dermatome
Dorsal root of spinal nerve
Level 9: Computer-aided 3-D Brain Reconstruction
Anterior cardinal vein
305
Central neural structures labeled
Brain surface (heavier line)
MESENCEPHALON
Tectal primordial plexiform layer
TECTUM
Mesencephalic roof plate
mesencephalic superventricle
Tectal NEP
Tegmental/isthmal primordial plexiform layer
(future aqueduct)
Migrating tegmental/isthmal neurons Migrating trigeminal (V) neurons Central trigeminal tract
isthmal canal
TEGMENTUM/ISTHMUS
Tegmental/isthmal NEP
PONS
PROPOSED RHOMBOMERE IDENTITIES R2
R2 (trigeminal NEP) rhombencephalic superventricle (future fourth ventricle)
R3 (facial sensory NEP)
Migrating facial sensory (VII) neurons? R4 (vestibulo-auditory NEP)
Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R3 Facial sensory NEP germinal source of sensory neurons that receive input from the facial (VII) ganglion. R4+5 Vestibulo-auditory NEP - germinal sources of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
Peripheral neural structure
R5 (vestibulo-auditory NEP) Migrating auditory and vestibular neurons
Lower medullary NEP
Migrating vestibulocochlear ganglionic neurons (VIII) from germinal source in otic vesicle epithelium Arrows indicate the presumed direction of neuron migration from germinal sources.
Migrating hypoglossal (XII) and vagal motor (X) neurons?
(vagal motor [X], hypoglossal [XII], blends with ventral spinal NEP)
MEDULLA
PLATE 141B
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Medullary floor plate
(midline raphe glial structure GEP?)
RHOMBENCEPHALON
SPINAL CORD Spinal floor plate
(midline raphe glial structure GEP)
Ventral funiculus Ventral gray
Ventral NEP
Spinal germinal zones
Intermediate gray ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Lateral funiculus Dorsal gray
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Dorsal Transient structure - Times bold italic Permanent structure - Times Roman or Bold funiculus
Intermediate NEP central canal
Dorsal NEP Spinal roof plate
306
Peripheral neural and non-neural structures labeled
PLATE 142A GW4.5 Coronal CR 6.3 mm M2300 Level 10: Section 155
*Boundary caps are Schwann cell GEPs?
Primordial mesenchymal brain case (skin, bone, and meninges)
Trigeminal boundary cap*
Fused maxillary process and mandibular arch (I)
Trigeminal ganglion (V) VIII nerve boundary caps* Vestibulocochlear ganglion (VIII) Migrating vestibulocochlear ganglionic neurons from germinal source in the otic epithelium Hyoid arch (II)
Anterior cardinal vein
Otic vesicle Epithelium Lumen
Glossopharyngeal ganglion (IX)
Vagal ganglion (X)
Dermatome
Dorsal root of spinal nerve
Level 10: Computer-aided 3-D Brain Reconstruction
307
Central neural structures labeled
Brain surface (heavier line)
MESENCEPHALON
PLATE 142B
Tectal primordial plexiform layer
TECTUM
Mesencephalic roof plate Tectal NEP
mesencephalic superventricle (future aqueduct)
isthmal canal
Isthmal primordial plexiform layer
ISTHMUS
Isthmal NEP
PROPOSED RHOMBOMERE IDENTITIES
CEREBELLUM
R2
Cerebellar NEP
Migrating cerebellar deep nuclear neurons R3
PONS Central trigeminal tract
rhombencephalic superventricle
R2 (trigeminal NEP) Migrating trigeminal (V) neurons
R4
(future fourth ventricle)
R3 (facial sensory NEP) Migrating facial sensory (VII) neurons?
R5
R4 (vestibulo-auditory NEP) R6 R5 (vestibulo-auditory NEP)
R6 (glossopharyngeal) NEP
Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
Migrating auditory and vestibular neurons Migrating glossopharyngeal receptor neurons (solitary nucleus?)
Lower medullary NEP
(vagal motor [X], hypoglossal [XII], blends with ventral spinal NEP)
Migrating hypoglossal (XII) and vagal motor (X) neurons?
MEDULLA
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
SPINAL CORD Ventral gray Ventral funiculus?
Intermediate gray Lateral funiculus
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: Dorsal ventricular divisions - capitals funiculus Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Ventral NEP
Spinal germinal Intermediate zones NEP
central canal
Dorsal NEP Spinal roof plate
308
PLATE 143A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 11: Section 165 Primordial mesenchymal brain case (skin, bone, and meninges)
*Boundary caps are Schwann cell GEPs?
VII nerve boundary cap?* Vestibulocochlear ganglion (VIII) VIII nerve Migrating vestibulocochlear ganglionic neurons from germinal source in the otic epithelium
VIII nerve boundary cap*
Otic vesicle Epithelium Lumen
Glossopharyngeal ganglion (IX)
Vagal ganglion (X)
Dermatome Dorsal root of spinal nerve
Level 11: Computer-aided 3-D Brain Reconstruction
309
PLATE 143B
Central neural structures labeled MESENCEPHALON TECTUM?
Brain surface (heavier line)
Mesencephalic roof plate Posterior tip of tectal NEP?
Tectal primordial plexiform layer? mesencephalic superventricle (future aqueduct)
ISTHMUS isthmal canal
Isthmal primordial plexiform layer
Isthmal NEP CEREBELLUM
PROPOSED RHOMBOMERE IDENTITIES
Fibrous layer in superficial cerebellum
R2
Cerebellar NEP
PONS
R3
rhombencephalic superventricle
R2 (trigeminal NEP) Central trigeminal tract
(future fourth ventricle)
R3 (facial sensory NEP) Migrating facial sensory (VII) neurons?
R4
R4 (vestibulo-auditory NEP) Migrating vestibular and auditory neurons
R5
R5 (vestibulo-auditory NEP) Migrating vestibular and auditory neurons
R6
R6 (glossopharyngeal) NEP Migrating glossopharyngeal receptor neurons (solitary nucleus?) R7 R7 (vagal sensory) NEP Migrating sensory vagal neurons?
Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Migrating hypoglossal (XII) and vagal motor (X) neurons?
Lower medullary NEP
MEDULLA
(vagal motor [X], hypoglossal [XII], blends with ventral spinal NEP)
RHOMBENCEPHALON
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Ventral funiculus? Ventral gray
SPINAL CORD Ventral NEP
Lateral funiculus Intermediate gray
Dorsal gray
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal funiculus
Intermediate NEP Spinal central canal
Dorsal NEP Spinal roof plate
germinal zones
310
PLATE 144A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 12: Section 185
Remnant of otic placode Primordial mesenchymal brain case (skin, bone, and meninges)
Otic vesicle Epithelium Lumen
Nerve X boundary cap (Schwann cell GEP?) Nerve X (vagus)
Nerve XI (spinal accessory)
Level 12: Computer-aided 3-D Brain Reconstruction
311
PLATE 144B
Central neural structures labeled RHOMBENCEPHALON CEREBELLUM
Medial metencephalic roof plate
Brain surface (heavier line)
Vermis
Cerebellar NEP
Fibrous layer in superficial cerebellum
Hemisphere
metencephalic pool
Lateral metencephalic roof plate in upper rhombic lip
rhombencephalic superventricle
PONS
(future fourth ventricle)
Auditory (cochlear) NEP? Migrating cochlear nuclear neurons?
Medullary velum
Lateral myelencephalic roof plate in lower rhombic lip PROPOSED RHOMBOMERE IDENTITIES
R4 (vestibulo-auditory NEP)
R4
Migrating vestibular and auditory neurons R5 (vestibulo-auditory NEP)
R5
myelencephalic pool
R6 (glossopharyngeal) NEP Migrating glossopharyngeal receptor neurons (solitary nucleus?)
R6
R7
R7 (vagal sensory) NEP Migrating sensory vagal neurons?
Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Midlateral medullary NEP
(blends with intermediate spinal NEP)
MEDULLA Lateral funiculus? Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Intermediate gray
SPINAL CORD Intermediate NEP
central canal Dorsal gray Dorsal funiculus
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal NEP Spinal roof plate
Spinal germinal zones
312
PLATE 145A
Peripheral neural and non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 13: Section 200
Primordial mesenchymal brain case (skin, bone, and meninges)
Otic vesicle Epithelium Lumen
Nerve IX boundary cap (Schwann cell GEP?)
Level 13: Computer-aided 3-D Brain Reconstruction
313
PLATE 145B
Central neural structures labeled
RHOMBENCEPHALON CEREBELLUM
Medial metencephalic roof plate
Brain surface (heavier line)
Vermis
Cerebellar NEP
Fibrous layer in superficial cerebellum
metencephalic pool
Hemisphere
Lateral metencephalic roof plate in upper rhombic lip
Medullary velum
MEDULLA
rhombencephalic superventricle
Precerebellar NEP
(future fourth ventricle)
Migrating precerebellar neurons
Lateral myelencephalic roof plate in lower rhombic lip
Migrating vestibular and auditory neurons R5 (vestibulo-auditory NEP)
R6 (glossopharyngeal) NEP Migrating glossopharyngeal receptor neurons (solitary nucleus?)
myelencephalic pool
R7 (vagal sensory) NEP? Migrating sensory vagal neurons? PROPOSED RHOMBOMERE IDENTITIES
Posteromedial medullary NEP
(blends with dorsal spinal NEP)
R5
Cuneate nuclear NEP? Migrating gracile and cuneate nuclear neurons?
R6
Gracile nuclear NEP?
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
R7
Medial myelencephalic roof plate
Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei. Arrows indicate the presumed direction of neuron migration from germinal sources.
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
314
PLATE 146A
Non-neural structures labeled
GW4.5 Coronal CR 6.3 mm M2300 Level 14: Section 210
Primordial mesenchymal brain case (skin, bone, and meninges)
Level 14: Computer-aided 3-D Brain Reconstruction
315
PLATE 146B
Central neural structures labeled
RHOMBENCEPHALON Medial metencephalic roof plate metencephalic pool
Medullary velum
rhombencephalic superventricle (future fourth ventricle)
MEDULLA
Precerebellar NEP Migrating precerebellar neurons myelencephalic pool Cuneate nuclear NEP?
Lateral myelencephalic roof plate in lower rhombic lip
Posteromedial medullary NEP
(blends with dorsal spinal NEP)
NEP - neuroepithelium Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating gracile and cuneate nuclear neurons? Gracile nuclear NEP?
Brain surface (heavier line)
Medial myelencephalic roof plate
316
PART PARTXII: XII: GW4 GW4 SAGITTAL SAGITTAL
Carnegie Collection specimen #9297 (designated here as C9297) with a 4.5-mm crown-rump length (CR) is estimated to be at gestational week (GW) 4. C9297 was embedded in a celloidin/paraffin mix and was cut in 8-µm sagittal sections that were stained with azan. Various orientations of the computer-aided 3-D reconstruction of C836’s brain are used to show the gross external features of a GW4 brain (Figure 11). Like most sagittally cut specimens, C9297’s sections are not parallel to the midline; Figure 11 shows the approximate rotations in front (B) and back views (C). We photographed 18 sections at low magnification from the left to right sides of the brain. Nine of the sections, mainly from the left side of the brain, are illustrated in Plates 147AB to 155AB. Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify the approximate midline, non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (lowcontrast images) identify central neural structures. Plates 132AB to 133AB show high-magnification views of the rhombencephalon. The prosencephalon is the smallest major brain structure with little distinction between a future telencephalon and diencephalon. The entire prosencephalic neuroepithelium is rapidly stockbuilding its various populations of neuronal and glial stem cells. The lamina terminalis in the ventral prosencephalon marks the site of closure of the anterior neuropore. A cell-dense area adjacent to the olfactory placode may be supporting cells associated with growth of the olfactory nerve toward the brain. The mesencephalon is much smaller than at GW5. The stockbuilding pretectal and tectal neuroepithelia have a relatively short anteroposterior length and blend with the
presumptive cerebellar neuroepithelium in the dorsomecial rhombencephalon. The stockbuilding tegmental and isthmal neuroepithelia form a distinctive arch between the mesencephalic and diencephalic flexures. There is a very thin subpial fiber band in the tegmentum and isthmus. The rhombencephalon is the largest brain structure. Rhombomeres 2 through 7 form well-defined swellings in the lateral neuroepithelium. Most sensory cranial ganglia and the otic vesicle are located directly lateral to the rhombomeres with which they interact. The trigeminal ganglion (V afferents) appears in sections lateral to the last section that contains rhombomere 2. The vestibulocochlear ganglion (VIII afferents) is lateral to the last section that contains rhombomere 4; the otic vesicle is lateral to the last section that contains rhombomere 5. The presumptive superior glossopharyngeal ganglion (IX afferents) is lateral to the last section with rhombomere 6, and the large superior vagal ganglion (X afferents) is lateral to the last section with rhombomere 7. The association of rhombomere 3 with the sensory part of nerve VII is less clear, but the facial ganglion (VII afferents) is near its presumptive placodal source in lateral sections. Each rhombomere has a thin layer of pioneer migrating neurons that are only visible in most lateral sections, where the outer edges of the rhombomeric neuroepithelium are cut tangentially. Virtually no fibers have yet entered the brain from these ganglia. Sections near the midline show a smooth neuroepithelium. Some migrating cells are outside the lower medullary neuroepithelium, and the subpial fiber band is thicker as the brain blends with the spinal cord. The cerebellum stands out as the most immature and smallest rhombencephalic structure. The most lateral sections show a very thin layer of migrating neurons outside the cerebellar neuroepithelium.
317
EXTERNAL FEATURES OF THE GW4 BRAIN
Ve n tr
al die n c
ep
entu
Is
3
thm
s
h
u C
us
Rhombomere (R) 2
n
T
on
4
ct
m ellu eb er
Optic vesicle
m eg
Te
m
C E P H N E e n c e p hal o l Te
n
Pretectum
l n rsa Do phalo n ce d ie
m
A
L
O
N
al
Side view
P R
A.
O
S
P
o
R3 R4
R5
M
A perfect sagittal cut through the brain is parallel to the midline from anterior to posterior. Sections of C9297's brain rotate an estimated 9.6º counterclockwise from the midline, 4.8º to the left Upper side of the anterior midline (B, rhombic front view), and 4.8º to the right lip side of the posterior midline (C, back view). In the sections illustrated on the following pages, anterior parts (top and left) are tilted toward the observer, while posterior parts (bottom and right) are tilted away from the observer. Medullary velum
e d
R6
BRAINSTEM FLEXURES R7?
l a u l
1
MESENCEPHALON
Front view
3. Mesencephalic 4. Diencephalic
Lower rhombic lip
Anterior midline
B.
1. Medullary
Spinal cord
C.
Pretectum
Back view
Tectum
Left side -4.8º
e e b l l
Right side
Posterior midline
e
u
r
PROSENOptic CEPHALON vesicle
Optic vesicle
C
m
Right side
R4 R5
Left side
Pons
R6 Rhombic lip border
R7?
RHOMBENCEPHALON
Spinal cord
Scale bars = 0.25 mm
Figure 11. A, The lateral view of the left side of a computer-aided 3-D reconstruction of the brain and upper cervical spinal cord in C836, the following GW4 specimen, which has a similar crown-rump length to C9297 (4.5 mm and 4.0 mm, respectively). External features are identified as in Figure 12B. The heavy numbered lines refer to brainstem flexures (boxed key). B, Front view of the brain in A. The angled line shows how C9297's sections rotate left (arrow) from the anterior midline. C, Back view of the brain in A. The angled line shows how C9297's sections rotate right (arrow) from the posterior midline.
Medullary velum
Medulla
-4.8º
Spinal cord
Medulla
318
PLATE 147A
GW4 Sagittal, CR 4.5 mm, C9297 Level 1: Slide 4, Section 32 LE
mesencephalic superventricle
Primordial mesenchymal brain case (skin, bone, and meninges)
FT
(future aqueduct)
SI
DE
O
F
A
I
ncepha d
ie
metencephalic pool
A RE E A
Rathke's pouch epithelium (primordium of anterior pituitary gland)
IN
prosencephalic superventricle
DL
li
c
p su
Cell-sparse superarachnoid reticulum
MI
elenceph re t a tu ventricl lic fu super e
er
ve
ntri
cle
BR
N
isthmal narrows canal
fu
tu
r
e
Medullary velum
Cephalic preplacode
al Or ty vi ca
uee nggu toton oof f diaia oordr imim PPr r
Mandibular arch (I)
Hyoid arch (II)
rhombencephalic superventricle
(future fourth ventricle)
Branchial placodes
Medullary velum
Pharynx
RIG HT
SI D
Larynx?
myelencephalic pool E
OF BR A
Gut
IN ND
SP
IN
A
L
C
O
RD
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
A
Vertebral/ basilar artery?
PLATE 147B
SENCEPHAL ME ON
ct ete Pr
P al NE
Mesencephalic (tectal) NEP
Posterior commissural GEP?
Mesencephalic (tegmental) NEP
Epithalamic
PR OS E
Dorsal diencephalic NEP
Isthmal NEP
NC E
Brain surface (heavier line)
P Anterior
) ALON
GE
P
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Fibrous processes
R H O M B E N C E P H A L O
A N D DIENCEPH
Posterior
a
ine ra p he gl i al
CE
Preoptic
h
l
dl
EN
ON
t
a
Mi
EL
o H y p
AL
i c
Ventral diencephalic NEP
Pontine NEP
Midline raphe glial structure
ET
ro
Lamina terminalis (site of anterior neuropore closure)
Upper rhombic lip
m
Basal telencephalic and septal
se
(F U T U R
Cerebral cortical
M id dl e
ALON
h ncep alic NE
P
PH
PH
Cerebellar NEP (vermis)
Thalamic
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Upp
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
er
Migrating medullary (reticular formation?) neurons Ascending fiber tracts from spinal cord
Migrating hypoglossal (XII) and vagal motor (X) neurons?
N
Labeled on this page: Central neural structures
L
fu n
ic u l
Lower rhombic lip Precerebellar NEP?
E P Low er
lu s n ic u a l fu r t n Ve y gra tr a l Ven
al a te r
Reticular, raphe, vagal motor (X), and hypoglossal (XII) NEPs?
N
M e d u l l a r y
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
y gra ate i d e erm Int
us
ray sal g Dor us nicul al fu Dors
Gracile and cuneate nuclear NEPs?
Spinal NEP
AL S PIN
D COR
Migrating gracile and cuneate nuclear neurons?
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
319
320
PLATE 148A
GW4 Sagittal, CR 4.5 mm, C9297 Level 2: Slide 4, Section 24 P lan
mesencephalic superventricle
Primordial mesenchymal brain case (skin, bone, and meninges)
eo
fs
ec
ti o
(future aqueduct)
ns
hi
fts
pr og re s
y
le
vl
r
ic
ate el or m
Cell-sparse superarachnoid reticulum
n
t
r
v
e
pe alic su
l
metencephalic pool
p
h
prosencephalic superventricle
ra
elenceph re t a tu ventricl lic fu super e
si
en future di
c
e
Rathke's pouch epithelium (primordium of anterior pituitary gland)
Cephalic preplacode
l
of
(future fourth ventricle)
ton
O F
e
v i t y c a
gu
B R A I N
Hyoid arch (II) Notochord
myelencephalic pool
Pharynx
MID LIN
E RI G HT
S
Medullary velum
ID E
Basilar artery?
OF BR AI N
AN
D
SP
AL IN
CO
RD
al tr al n ce can
Labeled on this page: Peripheral neural and nonneural structures, brain ventricular divisions
S I D E
ia
a
ord
r
im
Plates 156A and B: prosencephalon Plates 157A and B: isthmus, cerebellum, and pons Plates 160A and B: midline raphe glial structure
Branchial placodes
rhombencephalic superventricle
O
Pr
Mandibular arch (I)
See the following for higher magnification views of this section.
F T L E
Medullary velum
321
PLATE 148B
CEPHA MESEN LO N ctal NEP ete Pr
Mesencephalic (tectal) NEP
m
SE N CE P
T
h
a
l
a
HA L PH
LO
NA
i c
Brain surface (heavier line)
(reticular, raphe, abducens [VI], and facial motor [VII]?)
l o H y p Preoptic
ND
DIE N
Anterior
C E P H A LO N )
t
h
Upper rhombic lip
Pontine NEPs
a
a
r
P
CE A
Medial cerebellar notch?
m
Ventral diencephalic NEP
Cerebellar NEP
Migrating isthmal neurons
M id dl e
nc e os
EN
Basal telencephalic and basal ganglionic
Isthmal NEP
Migrating pontine (reticular, raphe, abducens [VI], and facial motor [VII]?) neurons
r U ppe
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medullary NEPs
(reticular, raphe, vagal motor [X], and hypoglossal [XII]?)
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
B E N C E P H A L O N O M R H
(F U T URE TEL
ephalic NEP
ON
Lamina terminalis (site of anterior neuropore closure)
Cerebral cortical
Posterior
c
Dorsal diencephalic NEP i
PR O
ic al EP ph ) N e l c a en nt es e M egm (t Migrating tegmental neurons
Epithalamic
Pioneer migrating cerebellar deep nuclear neurons?
Migrating trochlear neurons?
Posterior commissural GEP?
Lower
Midline raphe glial structure
Fibrous processes
Midline raphe glial GEP
Lower rhombic lip
tral Ven e diat rme Inte
Labeled on this page: Central neural structures
Spinal NEP
sal Dor
I N S P
A
L
C
O
R
D
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
322
PLATE 149A
GW4 Sagittal, CR 4.5 mm, C9297 Level 3: Slide 4, Section 16
mesencephalic superventricle
(future aqueduct)
eo fs
enc di
l r a
S I D E
f
Laryngotracheal groove
L E F T
c a v i t y
Hyoid arch (II)
ral
rhombencephalic superventricle
(future fourth ventricle)
O
Branchial placodes
e late mor
Medullary velum
Cephalic preplacode
Mandibular arch (I)
ivly ress rog ts p
metencephalic pool
Rathke's pouch epithelium (primordium of anterior pituitary gland)
e
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
h if
futur
ns
ephal
Cell-sparse superarachnoid reticulum
tio
prosencephalic superventricle
ec
telencep re rventr ha l ic e tu le i u sup
an
c
Pl
ic superventricle
Primordial mesenchymal brain case (skin, bone, and meninges)
Medullary velum
Lung bud?
Pharynx
O F B
myelencephalic pool
R
A
I
N
A N
Notochord
D S P
I A
L C
O
R
D
E L I N M I D
a
c
n
N
r n t e c
l
a
l
a
323
P
Te gm en ta l
ic m
Migrating tegmental neurons?
halamic
Brain surface (heavier line)
Migrating subthalamic neurons?
Cerebellar NEP
Subt ior
i c
er
m
po
st
l a
P
e/
a
dl
h
M
id
Anterior
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
R2
Migrating facial (VII) neurons from R3 NEP
Migrating vestibular and auditory neurons from R4+R5 NEPs
R5
Migrating medullary neurons
Medullary NEP
r
l ra ? nt te e ia V ed rm te In
r
PR O S EN CE P
te pla r ) o Flo GEP? ( All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
R6
Lo we
R6
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
l medullary NEP (reticula r , r a Media phe r [X], and hypoglossal , [XII l moto ] ?) vaga
R5
Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
Upper
R4
Pontine NEP
R3
PROPOSED RHOMBOMERE IDENTITIES
R3
Medial cerebellar notch? Upper rhombic lip
R4
Lamina terminalis (site of anterior neuropore closure)
R2
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
C E P H A L O M B E N O N R H
TELENC TURE EPH (FU AL N O ON L a A l h i p c e AN NE H enc s P D o
Ventral Basal telencephalic diencephalic and basal NEP ganglionic
t H y p o
E P
Dorsal diencephalic NEP
Cerebral cortical
Preoptic
L
la
P NE
Pioneer migrating cerebellar deep nuclear neurons
N
a
Epithalamic
Mesencephalic NEPS
l
Th
T e c t
a
N) LO A PH CE N E DI
tectal NEP re
PLATE 149B
A
ON
Labeled on this page: Central neural structures
MESE NCE PH
R
oof
pla
Sp
in
N al Do
te
C I N S P
A
L
EP
l rsa
O
R
D
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE ?A 150A
GW4 Sagittal, CR 4.5 mm, C9297 Level 4: Slide 4, Section 8 P lan
rv pe
en
cephal
ic
su
hi
fts
pr og re s
s
ral
di
pr su ose pe nc rv ep en ha t r l ic ic l e
ns
metencephalic pool Medullary velum
O F
B R A I N
c a v i t y
Branchial placodes
S I D E
l r a
Hyoid arch (II)
rhombencephalic superventricle
O
Mandibular arch (I)
(future fourth ventricle)
Cephalic recess preplacode
F T L E
optic
Lung bud?
ti o
Carotid artery?
futu r e
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
ec
ate
Cell-sparse superarachnoid reticulum Rathke's pouch epithelium (primordium of anterior pituitary gland)
fs
el or m
ic al ph cle
le
eo
ly iv
e n t ri c
Primordial mesenchymal brain case (skin, bone, and meninges)
future t e super len ve ce nt ri
324
Arch III
Pharynx
A N D
myelencephalic pool
S P I N
A
Cell-sparse superarachnoid reticulum
L C
O R
Vertebral/basilar artery?
D
325
Labeled on this page: Central neural structures
H
ic
Pioneer migrating cerebellar deep nuclear neurons
ar e ll b re P Ce NE
ic
Migrating subthalamic neurons
EP
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
EP
P
r
SENCEPHALON ( PRO F UT UR R7
Lower rhombic lip
Migrating medullary neurons
Ascending fiber tracts from spinal cord?
nuc lear NEP
R6
Migrating spinal motor neurons? Ventral funiculus
a l t r n V e
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
Medullary NEP
R7?
Migrating vagal sensory (X) neurons from R7 NEP
Lower
R5
R6
ac ile an dc un eat e
R4
R5
s p
i n
a
l
N
i n
E
a
Gr
P
l
N
E
P p E s N e t l a i a i n e d p m D r s t e R I n a l O s r C D o
I N S P
A
L
N C E P H M B E A L O N H O
R4
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
R
Brain surface (heavier line)
Upper
R3
Pontine NEP
R3
Migrating vestibular and auditory neurons from R4+R5 NEPs
R2
Upper rhombic lip
R2
Migrating facial (VII) neurons from R3 NEP
N le Optic vesic
PROPOSED RHOMBOMERE IDENTITIES
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Superficial fibrous layer
Medial cerebellar notch?
Basal telencephalic and basal ganglionic
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
Migrating pretectal and tectal neurons
lam
Diencephalic NEPs
Subtha
Cerebral cortical
m
an dG
LON AND EPHA DIE NC E NC L encephalic EP s TE o N H E A
P
la
O AL N
E
a Th
Tectal NEP
Pretectal NEP
Epithalamic
N) LO
PLATE 150B
MESENC EP
P
Arrows indicate the presumed direction of axon growth in brain fiber tracts. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 151A
GW4 Sagittal, CR 4.5 mm, C9297 Level 5: Slide 3, Section 40
Primordial mesenchymal brain case (skin, bone, and meninges)
Labeled on this page: Peripheral neural and non-neural structures, Pl an brain ventricular eo fs divisions e ct
Cell-sparse superarachnoid reticulum
n io sh
ift
alic enceph rhomb ventricleicle) ventr supefr ourth
(f u t u r
Maxillary process?
e
O r
Mandibular arch (I)
a
l Arch III
L E F T
Hyoid arch (II)
v i t y c a
S I D E
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
l
Medullary velum
Cephalic preplacode
Branchial placodes
tera
Cell-dense mesenchyme
a re l mo
optic recess
metencephalic pool
ly siv res rog sp
prosencephalic superventricle
myelencephalic pool
O F
Ph
ar
yn
x
Arch IV
B R A I N
Cell-sparse superarachnoid reticulum
Lung bud?
A N
D
Primitive gut?
S P
I
Vertebral artery?
N A L
Vertebral column
O
R
D
See Plates 158A and B for a high magnification view of the rhombencephalon.
C
326
327
PLATE 151B
Labeled on this page: Central neural structures Epithalamic
CE
Superficial fibrous layer
an d
R2
os
e
P
eN Optic vesicl
Migrating facial (VII) neurons from R3 NEP
)
Pontine NEP
R3 R4
R2 R3
R6
R7?
Lower rhombic lip
Migrating medullary neurons
Ascending fiber tracts from spinal cord?
Lateral funiculus? Intermediate gray
In
Dorsal gray
Dorsal funiculus
S P
I N
A
r te
L
m
ed
D
o
ia
te
a rs
C
l
O
s
N
s
E
in
p
Ventral gray Ventral funiculus
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
P
al
N
EP
R7
Migrating vagal sensory (X) neurons from R7 NEP
Medullary NEP
Prece r e b e llar NE P?
R5
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
R6
Lower
R4
R5
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
PROPOSED RHOMBOMERE IDENTITIES
Upper
Migrating vestibular and auditory neurons from R4+R5 NEPs
C E P H A L O N B E N O M
D I EN C E P H A L O N
E
H
CE
AND
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
R
EN
ON
P laEr) rlN llaehere eb b e rer spP e) C Ce(ehemNi Espher mi Upper (he rhombic lip
Medial cerebellar notch?
Basal telencephalic and basal ganglionic
nc
T U R E TEL
Cerebral cortical
Pioneer migrating cerebellar deep nuclear neurons
Brain surface (heavier line)
P
ephalic N E
Diencephalic NEPs
Pr
(F U
AL
ic
G EP
EN
LO N
H
a
m la
t h alamic Sub
OS PR
PH A
Th
P
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
p
in
R
a
l
D
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 152A
GW4 Sagittal, CR 4.5 mm, C9297 Level 6: Slide 3, Section 32
Plane of section shif ts p rog res s
Primordial mesenchymal brain case (skin, bone, and meninges)
ivl y
mo
re l
ate
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
ra l
prosencephalic superventricle
Cell-sparse superarachnoid reticulum
L T EF
DE SI
a l c
y/Ph
Hyoid arch (II)
Nerve IX boundary cap?*
arynx
Arch III
Cell-sparse superarachnoid reticulum
Arch IV
Nerve X boundary cap?*
Basal occipital bone?
r io
rc
ar
d in
al v ein ?
*Boundary caps are Schwann cell GEPs?
Lung bud?
myelencephalic pool
vit
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Otic vesicle epithelium
ra
Branchial placodes
Mandibular arch (I)
Nerve VIII boundary cap*
O
Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
a l ic
Maxillary process
eph
Nerve VII boundary cap?*
Preplacodal epithelium (maxillary)
An
)?
Primitive gut?
cc
es
so
ry
Vertebral column
Dorsal root ganglia Ne
AIN BR OF
Cell-dense mesenchyme
nc icle e) mbe ntr tricl rho perveth ven su e four ur (fut
metencephalic pool
optic recess
te
328
r
XI ve
(s
n pi
al
a
Medullary velum
329
PLATE 152B
Labeled on this page: Central neural structures PROSENCEPHALON
C
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Upper rhombic lip
R2
ne R3 N E
i
le
NE
P and
a lam
o
b th
Su
EP
e
Pioneer migrating cerebellar deep nuclear neurons
nt
O p tic v e s i c
Cerebellar NEP
Superficial fibrous layer
Po
ce sen pha ro rebral c
RHOMBENCEPHALON
Brain surface (heavier line)
G
P NE lic rtical
ic ?
(FUTURE TELENCEPHALON AND DIENCEPHALON)
Migrating facial sensory (VII) neurons from R3 NEP
P
P
R4
R6
Migrating vagal sensory (X) neurons from R7 NEP
r nuclear NEP?
R7
Cochlea
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
Lower rhombic lip
P N E
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
R5
y a r M e d u l l
Migrating vestibular and auditory neurons from R4+R5 NEPs
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4 R5 R6 R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
330
PLATE 153A
GW4 Sagittal, CR 4.5 mm, C9297 Level 7: Slide 3, Section 24
Plane o f
se c
ti o n
shi
fts
Primordial mesenchymal brain case (skin, bone, and meninges)
pro
gre
ssi vly
mo re l
at
er a
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
l
Cell-dense mesenchyme
Cell-sparse superarachnoid reticulum
optic recess
Nerve VII boundary cap?*
T LEF
Nasal process
Nerve V boundary cap?*
Nerve VIII boundary cap?*
EO
O
r
F BR
Maxillary process
al
Preplacodal epithelium (maxillary)
SID
Vestibulocochlear ganglion (VIII)
vi
ty
Germinal epithelium
ryn
Otic vesicle
x
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Lumen
ha
Branchial placodes
/P
Hyoid arch (II)
AIN
ca
Mandibular arch (I)
Nerve IX boundary cap?*
Arch III
Nerve X boundary cap?* Cell-sparse superarachnoid reticulum
Arch IV
Basal occipital bone?
Anterior cardinal vein?
Vagal ganglion (X)
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
*Boundary caps are Schwann cell GEPs?
Sy
Dorsal root ganglion
See a higher magnification view of the rhombencephalon in Plates 159A and B.
mp
at
tr tic he
un
k
g
g an
lia
?
331
PLATE 153B
Labeled on this page: Central neural structures
PROSENCEPHALON (FUTURE TELENCEPHALON AND DIENCEPHALON) RHOMBENCEPHALON
Prosencephalic (cerebral cortical)
NEP
Brain surface (heavier line)
icle NE es
Optic v
Migrating trigeminal nuclear complex (V) neurons from R2 NEP Migrating facial sensory (VII) neurons from R3 NEP?
R2 R3?
P
GEP and
Peripheral neural structure
Migrating vestibular and auditory (VIII) neurons from R5 NEP
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
Pontine NEP
R6
Medullary NEP
Migrating vagal sensory (X) neurons from R7 NEP
Arrows indicate the presumed direction of neuron migration from germinal sources.
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R5 R6 R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
PLATE 154A
GW4 Sagittal, CR 4.5 mm, C9297 Level 8: Slide 3, Section 16 P l a n e o f s e c ti o n s
Primordial mesenchymal brain case (skin, bone, and meninges)
h ifts p
rogre
ssiv
Ante rio r
ly m ore lat era l
in rd ca
Cell-dense mesenchyme
Labeled on this page: Non-neural structures, brain ventricular divisions
al
n? vei
optic recess
FT
SID
Nasal process
LE
Cell-sparse superarachnoid reticulum
EO
FB
Maxillary process
al
ca
vi
ty
Mandibular arch (I)
Y OD
Or
/P ha
ry
Branchial placodes
nx
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Hyoid arch (II) Arch III Arch IV
ca
vei
n?
n
i t e
te
s
ri
or
nal rdi
s
o
m
A
332
R
e
m
n
a
n
t
s
o
f
333 Labeled on this page: Peripheral neural structures
PLATE 154B Optic vesicle
(opthalmic germinal epithelia)
Pigment epithelium?
Trigeminal ganglion (V)
Preplacodal epithelium (maxillary)
Vestibulocochlear ganglion (VIII) Migrating vestibulocochlear ganglionic (VIII) neurons
e pi t
Olfactory placodal epithelium (germinal source of primary olfactory neurons)
Surface of optic evagination from the brain (heavier line)
h
e
Otic vesicle
u m l i
Lumen Luman
l
Optic nerve (II) GEP?
Retinal NEP?
m i n a e r
Sprouting nerve I (olfactory)
Oral and pharyngeal placodes
G
Intraretinal space
Retinal NEP?
Glossopharyngeal ganglion (IX) Placodal germinal source of ganglion IX? Placodal germinal source of ganglion X? Superior vagal ganglion (X)
Migrating vagal ganglionic (X) neurons? Inferior vagal ganglion (X)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of neuron migration from germinal sources.
(vestibulocochlear ganglionic germinal epithelia)
334
PLATE 155A
GW4 Sagittal, CR 4.5 mm, C9297 Level 9: Slide 3, Section 8
Primordial mesenchymal brain case (skin, bone, and meninges)
Plane of section
s hifts p
rogre
ssiv ly m ore l
optic recess
Cell-dense mesenchyme
Labeled on this page: Non-neural structures, brain ventricular divisions ate
ra
l
Cell-sparse superarachnoid reticulum
Nasal process
Maxillary process Mandibular arch (I) Branchial placodes
Hyoid arch (II)
Ph a rynx
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Oral cavity
Arch III Arch IV?
Anterior cardinal vein?
it
e
s
R
em
na
n
ts
of
s
om
DY F BO EO SID FT LE
Anterior cardinal vein?
335
PLATE 155B
Labeled on this page: Peripheral neural structures Optic vesicle
Sprouting opthalmic branch of Nerve V (trigeminal) with plentiful glia
(opthalmic germinal epithelia)
Pigment epithelium
a l s p a ce
t
Trigeminal ganglion (V)
Retinal NEP Placodal epithelium (maxillary) Optic nerve (II) GEP?
Olfactory placodal epithelium (germinal source of primary olfactory neurons)
Migrating facial ganglionic VII neurons?
Placodal germinal source of ganglion VII?
Oral and pharyngeal placodes
Vestibulocochlear ganglion (VIII) Facial ganglion (VII)
inal epi the rm
In trare
Sprouting nerve I (olfactory)
in
m liu
Lumen
Ge
Surface of optic evagination from the brain (heavier line)
Inferior Glossopharyngeal ganglion (IX)
Placodal germinal source of ganglion X?
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of neuron migration from germinal sources.
(vestibulocochlear ganglionic germinal epithelia)
Superior Glossopharyngeal ganglion (IX)
Placodal germinal source of ganglion IX?
Migrating vagal ganglionic (X) neurons?
Otic vesicle
Superior vagal ganglion (X) Nerve X (with plentiful glia) Inferior vagal ganglion (X)
336
PLATE 156A
SUBDIVISIONS OF THE PROSENCEPHALIC NEP
GW4 Sagittal CR 4.5 mm C9297 Level 1: Slide 4, Section 24
NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
See Level 2 in Plates 148A and B.
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
mesencephalic superventricle (future aqueduct)
Mesencephalic (tegmental) NEP
ic am
al
Th
Superficial fibrous layer may contain glial channels.
Dorsal diencephalic NEP
Pioneer migrating tegmental neurons?
Superficial fibrous layer may contain glial channels intermingled with pioneer axons from spinal cord, medulla, and pons.
P
m
Ventral diencephalic NEP
le
a
Rathke's pouch (evagination of the oral cavity)
a
l
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
dd
Future telencephalic NEP
i c
N
(future lateral and third ventricles)
E P
prosencephalic superventricle
Mi
al rebr Ce
Cell-sparse superarachnoid reticulum
Posterior (mammillary recess)
E
corti ca l
N
Pioneer migrating lateral mammillary nuclear neurons?
sa
lt
el
Preoptic NEP
Brain surface (heavier line)
en ce p
ha
li c
and
s ept
Lamina terminalis (site of anterior neuropore closure)
h
Ba
PROSENCEPHALON (FUTURE TELENCEPHALON AND DIENCEPHALON)
Primordial mesenchymal brain case (skin, bone, and meninges)
Mesencephalic (tegmental) NEP
MESENCEPHALON
NE
P
PLATE ?B 156B
Anterior
H
y
p
o
t
Rathke's pouch epithelium produces the diverse cell types in the anterior pituitary gland (adenohypophysis).
al N E P
Oral epithelium End of Rathke's pouch epithelium? Preplacodal epithelium
337
GW4 Sagittal CR 4.5 mm C9297 Level 2: Slide 4, Section 24
See Level 2 in Plates 148A and B.
ISTHMUS, CEREBELLUM, AND PONS
338
PLATE 157A
PLATE 157B NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Brain surface (heavier line)
Primordial mesenchymal brain case (skin, bone, and meninges)
Medullary velum
rhombencephalic superventricle
Upper rhombic lip
(future fourth ventricle) metencephalic pool
Pioneer migrating cerebellar deep nuclear neurons
Cerebellar NEP (vermis/hemisphere)
Superficial fibrous layer
Sprouting nerve IV (trochlear)?
Migrating tectal neurons
Medial pontine NEP
Tr oc hl ea rn uc le a rN EP ?
Migrating trochlear neurons?
Me (teg senc me eph nta alic l) N EP
(future aqueduct)
Medial cerebellar notch?
(reticular, raphe, abducens [VI], and facial motor [VII]?)
Isthmal NEP
Mesencephalic (tectal) NEP
mesencephalic superventricle
All parts of the NEP form expanding shorelines of the superventricles as stockbuilding NEP cells increase.
Migrating isthmal neurons Migrating tegmental neurons
MESENCEPHALON (TECTUM, TEGMENTUM, AND ISTHMUS)
Migrating pontine (reticular formation, abducens [VI], and facial motor [VII]?) neurons
Superficial fibrous layer may contain glial channels intermingled with pioneer axons from spinal cord and medulla.
Superarachnoid reticulum RHOMBENCEPHALON (CEREBELLUM AND PONS)
339
RHOMBOMERES IN PONS AND MEDULLA
GW4 Sagittal CR 4.5 mm C9297 Level 5: Slide 3, Section 40 Slide 3, Section 40 PROPOSED RHOMBOMERE IDENTITIES R2
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R3 Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. R4+5 Vestibulo-auditory NEP - germinal sources of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R6 Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. R7 Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
See Level 5 in Plates 151A and B.
340
PLATE ?A 158A
PLATE ?B 158B
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Arrows indicate the presumed direction of axon growth in brain fiber tracts.
Primordial mesenchymal brain case (skin, bone, and meninges) Brain surface (heavier line)
Medullary velum
Upper rhombic lip metencephalic pool
myelencephalic pool
rhombencephalic superventricle (future fourth ventricle)
Mitotic cells
Medullary NEP Cerebellar NEP
Pontine NEP
(hemisphere)
R4
Cerebellar notch?
R3
R2
(trigeminal NEP)
(facial NEP)
(vestibuloauditory NEP)
R5
(vestibuloauditory NEP)
R6
(glossopharyngeal NEP)
Pioneer migrating cerebellar deep nuclear neurons Superficial fibrous layer
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Migrating facial (VII) neurons from R3 NEP
Migrating vestibular and auditory (VIII) neurons from R4 and R5 NEPs
Migrating glossopharyngeal sensory neurons (IX) from R6 NEP
R7
(vagal sensory NEP)
Migrating vagal sensory (X) neurons from R7 NEP
Ascending axons from spinal cord?
341
GW4 Sagittal, CR 4.5 mm, C9297 Level 7: Slide 3, Section 24 See Level 7 in Plates 153A and B.
PROPOSED RHOMBOMERE IDENTITIES R2
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R3 Facial sensory NEP - germinal source of sensory neurons that receive input from the facial (VII) ganglion. R4+5 Vestibulo-auditory NEP - germinal sources of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R6 Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. R7 Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
RHOMBENCEPHALON AND SENSORY CRANIAL NERVE ENTRY ZONES
342
PLATE 159A
PLATE 159B
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
Arrows indicate the presumed direction of neuron migration from germinal sources.
Note that R4, R5, and R7 NEPs are not in the plane of this section.
Pontine NEP Migrating facial sensory (VII) neurons from R3 NEP?
Nerve VII boundary cap?*
1
Medullary NEP
Migrating vestibular and auditory (VIII) neurons from R5 NEP
Brain surface (heavier line)
R6 glossopharyngeal NEP
Nerve VIII boundary cap?*
1 Nerve V boundary cap?*
Primordial mesenchymal brain case (skin, bone, and meninges)
Migrating vagal sensory (X) neurons from R7 NEP
IX ?* rve cap Ne ary d un bo
R2 trigeminal NEP
R3? facial sensory NEP
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal) Nerve X (vagus)
Nerve X boundary cap?*
Vestibulocochlear ganglion (VIII)
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Lumen
Germinal epithelium
Migrating vestibulocochlear ganglionic (VIII) neurons from germinal source in otic epithelium
Migrating glossopharyngeal sensory neurons (IX) from R6 NEP
Cell-sparse superarachnoid reticulum
* Boundary caps are
Schwann cell GEPs?
Otic vesicle
343
GW4 Sagittal CR 4.5 mm C9297 Level 2: Slide 4, Section 24
See Level 2 in Plates 148A and B.
LOWER MEDULLA AND SPINAL CORD (MIDLINE RAPHE GLIAL STRUCTURE)
344
PLATE 160A
PLATE 160B ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medullary velum
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
rhombencephalic superventricle
(future fourth ventricle) myelencephalic pool
LEFT SIDE OF BRAIN
MIDLINE
End feet of NEP cells protrude into ventricule
Medullary NEP
(reticular, raphe, vagal motor [X], and hypoglossal [XII]?)
Midline raphe glial GEP (in cell body layer, no end feet)
RIGHT SIDE OF SPINAL CORD
central canal
Spinal NEP (ventral) Cell body layer
Fibrous processes
Midline raphe glial structure Notochord Oral cavity RHOMBENCEPHALON (LOWER MEDULLA)
Ventral commissural GEP? Ventral commissure in spinal cord SPINAL CORD
345
346
PART PARTXIII: XIII: GW4 GW4 CORONAL CORONAL
Carnegie Collection specimen #836 (designated here as C836) with a 4-mm crown-rump length (CR) is estimated to be at gestational week (GW) 4. C836 was fixed in corrosive acetic acid, embedded in paraffin, and was cut in 15-µm transverse sections that were stained with aluminum cochineal. Sections of the prosencephalon and anterior mesencephalon are cut in the coronal plane, but the plane shifts to predominantly horizontal in the posterior mesencephalon, pons, and medulla. We photographed 36 sections at low magnification from the frontal prominence to the posterior tips of the mesencephalon and medulla. Twelve of these sections are illustrated in Plates 161AB to 171AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of C836’s brain and optic vesicle (Figure 12), and to show each illustrated section in situ (insets, Plates 161A to 171A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify non-neural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. The prosencephalon is considerably smaller than at GW4.5 (Part XI) and consists of a stockbuilding neuroepithelium surrounding a small prosencephalic superventricle with paired optic recesses. Anterior sections are tentatively identified as future telencephalic neuroepithelium and include the semicircular olfactory placodes at the embryonic surface. The diencephalic neuroepithelium is located in-between and posterior to the large pair of optic vesicles that form the most prominent prosencephalic feature. A preplacodal epithelium is in the head around the optic vesicles, but a definite lens placode cannot be identified. The preplacodal epithelium is continuous with the
thickened olfactory placode anterolaterally and the primordium of Rathke’s pouch in the ventral midline. The mesencephalon contains a stockbuilding neuroepithelium surrounding a small mesencephalic superventricle. A roof (tectum) and floor (tegmentum) can be differentiated in coronally cut anterior sections. It is difficult to distinguish neuroepithelial subdivisions in posterior sections that cut the mesencephalon horizontally. A few pioneer migrating cells are outside the presumptive tegmental and isthmal neuroepithelia posteriorly. The primordial plexiform layer at the brain surface is very thin throughout the entire mesencephalon. The most prominent neuroepithelial structures in the rhombencephalon are the rhombomeric evaginations. This specimen is one of the best to show the “rippled” neuroepithelium in Plates 167 to 170. As in M2300 (Part XI), the trigeminal ganglion (sensory axons of V) is attached to the brain surface at rhombomere 2. The vestibulocochlear ganglion (source of VIII axons) is attached to the rhombomere 4 brain surface. The otic vesicle touches the rhombomere 5 brain surface. A glossopharyngeal ganglion is lateral to the brain at rhombomere 6. The short nerve extending from the large vagal ganglion (sensory axons of X) touches the rhombomere 7 brain surface. The facial ganglion is tentatively identified adjacent to a placode in the hyoid arch that lies immediately ventral to the vestibulocochlear ganglion and posteroventral to rhombomere 3. Very few neurons are migrating from the rhombomeres. The small stockbuilding cerebellar neuroepithelium is only identifiable in the most posterior sections of the rhombencephalon and is difficult to distinguish from the mesencephalic tectum.
347
C836 Computer-aided 3-D Brain Reconstructions B. Side view
S thala u
P R O
S
E
Up
rm
ha
n
R3
o
Preoptic area
R4
Medullary velum
R5 R6
a
R7
BRAINSTEM FLEXURES
u ll a
1
a ull ed rm
med
Future telencephalon
we
R7
R2
Lo
er
R6
4 3
ll
L
ow
R5
e d u ll a
t
Upper rhombic lip
s
ed u
pe
o Hy p
mu
per m Up
P
sth
P
s
n
o
R4
mentu
s
N C E P S E H O
Su
bth ala m
H A L O N E P
Optic vesicle R
R3
eg
um
C
b- s mu
e ll
N
Epithalamu s
lamus Tha
reb Ce
R h o m b o m e r e s
Preoptic area
Optic vesicle
Tectum
I
s R2
t e l F uture e n c ep h alo n
O
Pretectum
m
m entu gm
Isth mu
us
Te
us
llum e be Ce r
s mu
Thal am
L
A
Epithala
N
T
Tectum
Pretectum
l a m us
Angled front view
P
A.
1. Medullary 3. Mesencephalic
Lower rhombic lip
4. Diencephalic
Spinal cord
Spinal cord
C.
Top view
Optic vesicle
C e r e b e l l u m
h
m
u s
T e c t u m
r e t e c t u m P
E p i t h a l a m u s
a l a m u T h s
lencephal ure te on Fut
P
R
O
I s P o
t
n
s
Medullary velum
N C E P H A L S E
O
N
R2
Upper rhombic lip
Figure 12. A, The left side of the 3–D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures.
D.
Bottom view Optic vesicle
R7 d
R6
r C o
i n a l
p
r medu pe ll
p
R5 a
medu er ll w a
s
n o
P s
n o
I s t h m u s
m
u g m e n t
e
o t m u s h a l a H y p
a r e a
re telencepha Futu lo
P r e o p t i c
P
N
P
R
Scale bars = 0.25 mm
T
R3 R4
U
E N C E P H A O S L
O
R2
o
n
L
Subthalamus
S
348
PLATE 161A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836
Level 1: Section 9 Preplacodal epithelium
Primordial mesenchymal brain case (skin, bone, and meninges)
Olfactory placode
Level 1: Computer-aided 3-D Brain Reconstruction
Level 2: Section 27 Primordial mesenchymal brain case (skin, bone, and meninges)
Mesenchymal? densities near optic vesicle
Optic vesicle
Lens placode Preplacodal epithelium
Level 2: Computer-aided 3-D Brain Reconstruction
Rathke's pouch epithelium
349
PLATE 161B
Central neural structures labeled
Level 1: Section 9 PROSENCEPHALON
Brain surface (heavier line)
Prosencephalic roof plate
Prosencephalic primordial plexiform layer
Prosencephalic NEP
prosencephalic superventricle
(future telencephalic)
(future lateral and third ventricles)
Prosencephalic floor plate
DIENCEPHALON
Level 2: Section 27
THALAMUS
Diencephalic roof plate
(future choroid plexus in roof of third ventricle)
Thalamic primordial plexiform layer
Thalamic NEP
Brain surface (heavier line)
SUBTHALAMUS
Subthalamic NEP Subthalamic primordial plexiform layer
Preoptic area NEP? Pigment epithelium
Glial channels in retinal NEP?
diencephalic superventricle optic recess
(future third ventricle)
Preoptic primordial plexiform layer
Retinal NEP Anterior hypothalamic NEP Diencephalic floor plate
Hypothalamic primordial plexiform layer
(future chiasmal GEP)
PREOPTIC AREA/ HYPOTHALAMUS FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
350
PLATE 162A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 3: Section 36
Mesenchymal? densities near optic vesicle
Primordial mesenchymal brain case (skin, bone, and meninges)
Lens placode
Optic vesicle
Rathke's pouch epithelium Cephalic preplacode Lateral tongue primordia Part of the mandibular arch placodal epithelium gives rise to the thyroid gland.
Mandibular arch (I)
Arterial trunk
Liver
Peritoneal cavity
The GW4 Face and Neck
Figure 247A modified (Patten, 1953, p. 429.)
Frontal prominence Optic vesicle Olfactory placode Future oral cavity Tongue and mandible primordia
Maxillary process Mandibular arch (I)
Hyo-mandibular cleft Hyoid arch (II)
Level 3: Computer-aided 3-D Brain Reconstruction
Arches III and IV
351
PLATE 162B
Central neural structures labeled THALAMUS/EPITHALAMUS
Brain surface (heavier line)
Diencephalic roof plate
(future pineal gland?)
Thalamic/epithalamic NEP
pineal recess?
Thalamic/epithalamic primordial plexiform layer
Subthalamic primordial plexiform layer
SUBTHALAMUS
Pigment epithelium
Subthalamic NEP
optic recess
Opthalmic germinal epithelia
Retinal NEP
Anterior/middle hypothalamic NEP
diencephalic superventricle
(future third ventricle)
Diencephalic floor plate
Hypothalamic primordial plexiform layer
(future chiasmal GEP)
HYPOTHALAMUS Chiasmal glial channels?
DIENCEPHALON
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
352
Peripheral neural and non-neural structures labeled
PLATE 163A
Primordial mesenchymal brain case (skin, bone, and meninges)
GW4 Coronal CR 4.0 mm C836 Level 4: Section 48 Cell-sparse formative superarachnoid reticulum
Sphenoid primordium
Maxillary process Cephalic preplacode Rathke's pouch epithelium Future oral cavity
Migrating trigeminal ganglionic (V) neurons? Trigeminal ganglion (V) placode? Tongue primordia
Epithelium Lateral Medial
Mandibular arch (I)
Hyoid arch (II) Multiple loci in the branchial placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Arterial trunk Arch III?
Arch IV? Pharynx Vagal ganglion (X) placode? Vagal ganglion (X)
Dorsal aorta
Level 4: Computer-aided 3-D Brain Reconstruction
Laryngotracheal groove
353
Central neural structures labeled
PLATE 163B
THALAMUS/EPITHALAMUS
Brain surface (heavier line)
Diencephalic roof plate
(future pineal gland?)
Thalamic/epithalamic NEP
Thalamic/epithalamic primordial plexiform layer pineal recess?
SUBTHALAMUS Subthalamic primordial plexiform layer
Subthalamic NEP
diencephalic superventricle (future third ventricle)
mammillary/ infundibular recesses
Middle/posterior hypothalamic NEP
Hypothalamic primordial plexiform layer
Diencephalic floor plate
(future median eminence and neurohypophyseal GEP)
HYPOTHALAMUS
DIENCEPHALON
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from germinal sources. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
354
PLATE 164A GW4 Coronal CR 4.0 mm C836 Level 5: Section 63
Peripheral neural and non-neural structures labeled
Primordial mesenchymal brain case (skin, bone, and meninges)
Anterior cardinal vein Formative cell-sparse superarachnoid reticulum
Fused maxillary process and mandibular arch (I) Sphenoid primordium? Notochord
Trigeminal ganglion (V) placode?
Oral placodes
Oral cavity Hyoid arch (II)
Multiple loci in the branchial placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands. Arch III
Level 5: Computer-aided 3-D Brain Reconstruction
Pharynx Pharyngeal placodes
Arch IV?
Vagal ganglion (X) placode? Vagal ganglion (X)
Dorsal aorta Notochord
Anterior cardinal vein
Somites Dorsal root ganglion boundary cap (Schwann cell GEP?)
355
Central neural structures labeled
PLATE 164B
Brain surface (heavier line) Tectal primordial plexiform layer
TECTUM
Mesencephalic roof plate Tectal NEP
mesencephalic superventricle (future aqueduct)
TEGMENTUM
Tegmental primordial plexiform layer
Tegmental NEP Mesencephalic floor plate
Peripheral neural structures
(midline raphe glial structure GEP?)
(migrating peripheral ganglionic neurons from germinal sources in the branchial placodes)
MESENCEPHALON
Trigeminal ganglionic neurons (V)
Vagal ganglionic neurons (X)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Ventral gray
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
SPINAL CORD
Ventral funiculus
Spinal floor plate
(ventral commissural GEP)
Ventral NEP
Lateral funiculus Dorsal funiculus
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Intermediate NEP central canal
Dorsal NEP Spinal roof plate
Spinal germinal zones
356
Peripheral neural and non-neural structures labeled
PLATE 165A
Primordial mesenchymal brain case (skin, bone, and meninges) culum e r a r a c h n o i d r e ti
GW4 Coronal CR 4.0 mm C836 Level 6: Section 72
Fused maxillary process and mandibular arch (I)
Trigeminal ganglion (V) placode? Anterior cardinal vein
Forma tive
cellspar s
e sup
Trigeminal ganglion (V)
Facial ganglion (VII) placode Facial ganglion (VII)
Hyoid arch (II)
Glossopharyngeal ganglion (IX) placode?
Level 6: Computer-aided 3-D Brain Reconstruction
Arch III? Glossopharyngeal ganglion (IX) Vagal ganglion (X) placode? Vagal ganglion (X)
Arch IV?
Anterior cardinal vein
Somites
Dorsal root ganglion boundary cap (Schwann cell GEP?)
357
Central neural structures labeled
Brain surface (heavier line)
MESENCEPHALON TECTUM
PLATE 165B
Tectal primordial plexiform layer
Mesencephalic roof plate mesencephalic superventricle
Tectal NEP
(future aqueduct)
Tegmental/isthmal NEP Tegmental/isthmal primordial plexiform layer
isthmal canal
TEGMENTUM/ISTHMUS
Peripheral neural structures
(migrating peripheral ganglionic neurons from germinal sources in the branchial placodes)
PONS/MEDULLA Pontine primordial plexiform layer
R2 (trigeminal NEP)
Trigeminal ganglionic neurons (V)
rhombencephalic superventricle
(future fourth ventricle)
Midline raphe glial structure GEP? Facial ganglionic neurons (VII)
Medial pontine NEP Pontine primordial plexiform layer PROPOSED RHOMBOMERE IDENTITY R2
Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus.
Glossopharyngeal ganglionic neurons (IX)
Rhombencephalic floor plate (midline raphe glial structure GEP?)
Midline raphe glial structure Vagal ganglionic neurons (X)
Medullary primordial plexiform layer?
Lower medullary NEP? (fuses with ventral spinal NEP)
RHOMBENCEPHALON
SPINAL CORD Ventral NEP
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
Lateral funiculus
Dorsal funiculus
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
central canal
Intermediate NEP Dorsal NEP Spinal roof plate
Spinal germinal zones
358
Fused maxillary process and mandibular arch (I) Trigeminal boundary cap* Trigeminal ganglion (V) Trigeminal ganglion (V) placode?
Anterior cardinal vein
culum e r a r a c h n o i d r e ti
* Boundary caps are Schwann cell GEPs?
e sup
Primordial mesenchymal brain case (skin, bone, and meninges)
cellspar s
GW4 Coronal CR 4.0 mm C836 Level 7: Section 75
Peripheral neural and non-neural structures labeled
Forma tive
PLATE 166A
Facial ganglion (VII) placode Facial ganglion (VII)
Hyoid arch (II)
Glossopharyngeal ganglion (IX) placode? Glossopharyngeal ganglion (IX) Anterior cardinal vein Vagal ganglion (X)
Sympathetic trunk?
Somites
Dorsal root ganglion boundary cap*
Level 7: Computer-aided 3-D Brain Reconstruction
359 Central neural structures labeled
PLATE 166B
Brain surface (heavier line)
MESENCEPHALON
Tectal primordial plexiform layer
TECTUM
Mesencephalic roof plate
mesencephalic superventricle
Tectal NEP
(future aqueduct) Tegmental/isthmal primordial plexiform layer isthmal canal
TEGMENTUM/ISTHMUS
Tegmental/isthmal NEP Migrating tegmental/isthmal neurons
PONS Migrating trigeminal (V) neurons
Peripheral neural structures
(migrating peripheral ganglionic neurons from germinal sources in the branchial placodes)
Trigeminal ganglionic neurons (V)
R2 (trigeminal NEP) Central trigeminal tract
rhombencephalic superventricle
(future fourth ventricle)
Medial pontine NEP
(abducens [VI], facial motor [VII]?) Migrating abducens (VI) and facial motor (VII) neurons?
Facial ganglionic neurons (VII)
R4 (vestibulo-auditory NEP) Migrating vestibulo-auditory neurons from R4 NEP
Rhombencephalic floor plate (midline raphe glial structure GEP?)
Glossopharyngeal ganglionic neurons (IX)
rhombencephalic superventricle
(future fourth ventricle)
PROPOSED RHOMBOMERE IDENTITIES R2 Trigeminal NEP germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R4 Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
Medial medullary NEP
(vagal motor [X], hypoglossal [XII]?, blends with ventral spinal NEP) Migrating hypoglossal (XII) and vagal motor (X) neurons?
SPINAL CORD
MEDULLA
Ventral NEP
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Ventral gray
Intermediate NEP
Intermediate gray Lateral funiculus
central canal
Dorsal NEP Dorsal funiculus?
Spinal roof plate
Spinal germinal zones
360
PLATE 167A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 8: Section 81
Primordial mesenchymal brain case (skin, bone, and meninges)
Fused maxillary process and mandibular arch (I) Trigeminal boundary cap (Schwann cell GEP?)
Trigeminal ganglion (V)
Anterior cardinal vein Vestibulocochlear ganglion (VIII)
Otic vesicle epithelium
Glossopharyngeal ganglion (IX) placode? Glossopharyngeal ganglion (IX) Anterior cardinal vein Vagal ganglion (X) Sympathetic trunk?
Somites
Dorsal root ganglion boundary cap (Schwann cell GEP?)
Level 8: Computer-aided 3-D Brain Reconstruction
361
PLATE 167B
Central neural structures labeled MESENCEPHALON
Brain surface (heavier line)
Tectal primordial plexiform layer?
TECTUM?
Mesencephalic roof plate Posterior tip of tectal NEP?
ISTHMUS isthmal canal
Isthmal NEP
mesencephalic superventricle (future aqueduct)
Isthmal primordial plexiform layer
Early cell migration from rhombomeric NEPs
CEREBELLUM
Cerebellar NEP?
Fibrous layer in superficial cerebellum?
PONS
Migrating trigeminal (V)(V) neurons? Migrating trigeminal neuron
R2 (trigeminal NEP) PROPOSED RHOMBOMERE IDENTITIES
Migrating facial (VII) neurons
R3 (facial NEP)
R4 (vestibulo-auditory NEP) Migrating vestibulocochlear ganglionic neurons from germinal source in otic epithelium
R5 (vestibulo-auditory NEP Migrating vestibular and auditory neurons Migrating glossopharyngeal receptor neurons (solitary nucleus)
R6 (glossopharyngeal NEP) Migrating sensory vagal neurons
R7 (vagal sensory NEP) Lower intermediate medullary NEP (blends with intermediate spinal NEP)
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources.
Intermediate gray
Lateral funiculus
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal funiculus?
R3
(future fourth ventricle)
Migrating vestibular and auditory neurons
rhombencephalic superventricle
R2
R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
SPINAL CORD Intermediate NEP central canal
Spinal germinal Dorsal NEP zones Spinal roof plate
362
PLATE 168A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 9: Section 84
Primordial mesenchymal brain case (skin, bone, and meninges)
Fused maxillary process and mandibular arch (I)
Trigeminal ganglion (V) Trigeminal boundary cap*
* Boundary caps are Schwann cell GEPs?
Nerve VII boundary cap* Nerve VIII boundary cap*
Vestibulocochlear ganglion (VIII)
Otic vesicle Nerve V (trigeminal) Nerve VII (facial)
Lumen Epithelium Anterior cardinal vein
Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal)
Nerve IX boundary cap*
Nerve X (vagus) Nerve X boundary cap* Vagal ganglion (X)
Somites
Dorsal root ganglion boundary cap*
Level 9: Computer-aided 3-D Brain Reconstruction
363
Central neural structures labeled
PLATE 168B
MESENCEPHALON
Brain surface (heavier line) Tectal primordial plexiform layer?
TECTUM?
Mesencephalic roof plate Posterior tip of tectal NEP?
ISTHMUS
isthmal canal
Isthmal NEP
mesencephalic superventricle (future aqueduct)
Isthmal primordial plexiform layer
CEREBELLUM
Cerebellar NEP Fibrous layer in superficial cerebellum
Early cell migration from rhombomeric NEPs
PONS
Migrating trigeminal (V) neurons
R2 (trigeminal NEP) Migrating facial sensory (VII) neurons
PROPOSED RHOMBOMERE IDENTITIES
(future fourth ventricle)
R4 (vestibulo-auditory NEP)
rhombencephalic superventricle
R3 (facial NEP)
R5 (vestibulo-auditory NEP Migrating glossopharyngeal receptor neurons (solitary nucleus)
R6 (glossopharyngeal NEP) Migrating sensory vagal neurons
R7 (vagal sensory NEP)
Lower intermediate medullary NEP (blends with intermediate spinal NEP)
R2
R3
R4
R5
R6
R7
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources.
Intermediate gray
SPINAL CORD
Lateral funiculus
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal funiculus?
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Intermediate NEP central canal
Spinal germinal Dorsal NEP zones Spinal roof plate
364
PLATE 169A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 10: Section 90 Primordial mesenchymal brain case (skin, bone, and meninges)
Trigeminal ganglion (V)
Trigeminal boundary cap Nerve VII boundary cap*
* Boundary caps are Schwann cell GEPs?
Nerve VIII boundary cap* Vestibulocochlear ganglion (VIII)
Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear)
Otic vesicle
Lumen Epithelium
Nerve IX (glossopharyngeal) Nerve X (vagus) Glossopharyngeal ganglion (IX) Nerve IX boundary cap* Nerve X boundary cap* Vagal ganglion (X)
Somites?
Dorsal root ganglion *boundary cap
Level 10: Computer-aided 3-D Brain Reconstruction
365
PLATE 169B
Central neural structures labeled MESENCEPHALON
Brain surface (heavier line) Tectal primordial plexiform layer?
TECTUM?
Mesencephalic roof plate Posterior tip of tectal NEP?
ISTHMUS
mesencephalic superventricle isthmal canal
Isthmal NEP?
(future aqueduct) Isthmal primordial plexiform layer?
CEREBELLUM
Early cell migration from rhombomeric NEPs
Cerebellar NEP Fibrous layer in superficial cerebellum
PONS
R2 (trigeminal NEP) Migrating trigeminal (V) neurons
PROPOSED RHOMBOMERE IDENTITIES
R3 (facial NEP)
Migrating vestibular and auditory neurons
R5 (vestibulo-auditory NEP R6 (glossopharyngeal NEP) Migrating glossopharyngeal receptor neurons (solitary nucleus)
R7 (vagal sensory NEP) Migrating vagal sensory neurons
Lower intermediate medullary NEP (blends with intermediate spinal NEP)
R3
(future fourth ventricle)
R4 (vestibulo-auditory NEP)
rhombencephalic superventricle
R2
Migrating facial (VII) neurons
R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources.
SPINAL CORD Intermediate NEP
Intermediate gray Lateral funiculus
Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal funiculus?
central canal
Dorsal NEP
Spinal roof plate
Spinal germinal zones
366
PLATE 170A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 11: Section 93 Primordial mesenchymal brain case (skin, bone, and meninges)
Trigeminal (V) boundary cap?*
* Boundary caps are Schwann cell GEPs?
Nerve VII boundary cap*
Nerve VIII boundary cap* Migrating vestibulocochlear ganglionic (VIII) neurons? Nerve V (trigeminal) Nerve VII (facial) Nerve VIII (vestibulocochlear)
Otic vesicle
Lumen Epithelium
Nerve IX (glossopharyngeal) Nerve X (vagus) Glossopharyngeal ganglion (IX)? Nerve IX boundary cap* Nerve X boundary cap* Nerve X (vagus)
Level 11: Computer-aided 3-D Brain Reconstruction
Vestibulocochlear ganglion (VIII)
367
PLATE 170B
Central neural structures labeled Metencephalic roof plate
CEREBELLUM
Brain surface (heavier line)
Vermis
Cerebellar NEP
Hemisphere
Fibrous layer in superficial cerebellum
metencephalic pool
PONS
PROPOSED RHOMBOMERE IDENTITIES
R4 (vestibulo-auditory NEP) Migrating vestibular and auditory neurons
R5 (vestibuloauditory NEP
R6 (glossopharyngeal NEP) Migrating glossopharyngeal receptor neurons (solitary nucleus)
R7 (vagal sensory NEP) Migrating vagal sensory neurons
(future fourth ventricle)
Migrating facial (VII) neurons
rhombencephalic superventricle
R2 (trigeminal NEP) R3 (facial NEP)
Early cell migration from rhombomeric NEPs
R2
R3
R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Posteromedial medullary NEP
(gracile and cuneate nuclear NEP blends with dorsal spinal NEP)
myelencephalic pool
Migrating gracile and cuneate nuclear neurons?
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Myelencephalic roof plate
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
368
PLATE 171A
Peripheral neural and non-neural structures labeled
GW4 Coronal CR 4.0 mm C836 Level 12: Section 99 Primordial mesenchymal brain case (skin, bone, and meninges)
Nerve VIII boundary cap* Migrating vestibulocochlear ganglionic (VIII) neurons? Nerve VIII (vestibulocochlear) Nerve IX (glossopharyngeal)
Otic vesicle
Lumen Epithelium
* Boundary caps are Schwann cell GEPs? Nerve IX boundary cap*
Level 12: Computer-aided 3-D Brain Reconstruction
369
PLATE 171B
Central neural structures labeled Medial metencephalic roof plate CEREBELLUM Brain surface (heavier line)
Vermis
Cerebellar NEP
Hemisphere?
metencephalic pool
Lateral metencephalic roof plate
Future medullary velum
(lower rhombic lip)
Auditory (cochlear) NEP?
R5 (vestibuloauditory NEP
R6 (glossopharyngeal NEP)
Posteromedial medullary NEP
(gracile and cuneate nuclear NEP blends with dorsal spinal NEP)
(future fourth ventricle)
Lateral myelencephalic roof plate
rhombencephalic superventricle
(upper rhombic lip)
PROPOSED RHOMBOMERE IDENTITIES R5
R6
Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
myelencephalic pool
MEDULLA
RHOMBENCEPHALON ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medial myelencephalic roof plate
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the superventricle with increase in stockbuilding NEP cells.
370
PART PARTXIV: XIV: GW3.8 GW3.8 SAGITTAL SAGITTAL
Carnegie Collection specimen #7724 (designated here as C7724) has a 4-mm crown-rump length (CR). However, at this early stage, CR length is an unreliable estimate of gestational age. The right side of the body has clearly separated 24 to 25 somites with both anterior and posterior neuropores closed. Using the timetables in Patten (1953) and Hamilton et al. (1959), we estimate that C7724 is at gestational week (GW) 3.8. C7724 was fixed in formalin, was embedded in a celloidin/paraffin mix, and was cut in 8-µm sagittal sections that were stained with hematoxylin and eosin. Various orientations of the computer-aided 3-D reconstruction of C836’s brain are used to show the gross external features of a GW4 brain (Figure 13). Like most sagittally cut specimens, C7724’s sections are not parallel to the midline; Figure 13 shows the approximate rotations in front (B) and back views (C). We photographed 24 sections at low magnification from the left to right sides of the body. Eight of the sections, mainly from the left side of the body, are illustrated in Plates 172AB to 179AB. Each illustrated section shows the entire embryo. Labels in A Plates (normal-contrast images) identify the approximate midline, non-neural structures, peripheral neural structures, and brain ventricular divisions; labels in B Plates (lowcontrast images) identify central neural structures. Plates 180AB to 184AB show high-magnification views of several parts of the brain. The prosencephalon is the smallest major brain structure with little distinction between a future telencephalon and diencephalon. The entire prosencephalic neuroepithelium is rapidly stockbuilding its various populations of neuronal and glial stem cells surrounding a small prosencephalic protoventricle. The ventral and lateral prosencephalon is surrounded by cephalic preplacodes at the surface (for example, the anterolateral olfactory placode) that are continuous with those extending into the roof of the developing oral cavity (for example, Rathke’s pouch).
The mesencephalon is smaller than at GW4 but has similar developmental features. The stockbuilding pretectal and tectal neuroepithelia have a relatively short anteroposterior length and blend with the presumptive cerebellar neuroepithelium in the dorsomedial rhombencephalon. The stockbuilding tegmental and isthmal neuroepithelia form a distinctive arch between the mesencephalic and diencephalic flexures. These neuroepithelia surround a small mesencephalic protoventricle. There is a very thin subpial fiber band in the tegmentum and isthmus. The rhombencephalon is the largest brain structure. Rhombomeres 2 through 7 form well-defined swellings in the lateral neuroepithelium (Plate 176). As in the GW4 specimens, most sensory cranial ganglia and the otic vesicle are located directly lateral to the rhombomeres with which they interact. The trigeminal ganglion (source of sensory V axons) appears in sections lateral to the last section that contains rhombomere 2. The vestibulocochlear ganglion (VIII afferents) and the otic vesicle are lateral to the last section that contains rhombomeres 4 and 5. The presumptive glossopharyngeal ganglion (IX afferents) is ventrolateral to the last section with rhombomere 6, and the presumptive vagal nerve (X afferents) is lateral to the last section with rhombomere 7. The presumptive facial ganglion (VII afferents) is near a branchial placode in the hyoid arch, slightly posterior and ventrolateral to rhombomere 3. Each rhombomere has a thin layer of pioneer migrating neurons that are only visible in most lateral sections, where the outer edges of the rhombomeric neuroepithelium are cut tangentially. Sections through the midline show a smooth neuroepithelium. Some migrating cells are outside the lower medullary neuroepithelium. The primordial white matter in the spinal cord extends into the lower medulla. The cerebellum stands out as the most immature and smallest rhombencephalic structure that blends with the isthmal neuroepithelium laterally and the presumptive tectal neuroepithelium medially.
371
EXTERNAL FEATURES OF THE GW4.0 BRAIN
mentu
R7
s
A perfect sagittal cut through the brain is parallel to the midline from anterior to posterior. Sections of C7724's brain rotate an estimated 6.6º counterclockwise from the midline, 3.3º to the left side of the anterior midline (B, front view), and 3.3º to the right side of the posterior midline (C, back view). In the sections illustrated on the following pages, anterior parts (top and left) are tilted toward the observer, while posterior parts (bottom and right) are tilted away from the observer. The lower part of the spinal cord (not shown in this reconstruction) has a concave curve, and the sacral tip is cut in the coronal plane.
P H A L O N
l a u l
1
R6
N C E
P
o
E Medullary velum
R5
e d
P R
O
S
MESENCEPHALON
R4
M
Anterior midline
Front view
Upper rhombic lip
Rhombomere (R) 2
R3
Figure 13. The 3-D reconstruction of the brain and upper cervical spinal cord in C836 is used to show the approximate external features of C7724, a 24-25 somite embryo estimated to be 25 (Patten, 1953) to 28 (Hamilton et al., 1959) days old (average age = GW3.8). A, The lateral view of the left side. External features are identified as in Figure 12B. The heavy numbered lines refer to brainstem flexures (boxed key); the pontine flexure (#2 in preceding specimens) is not present. B, Front view of the brain in A. The angled line shows how C7724's sections rotate left (arrow) from the anterior midline. C, Back view of the brain in A. The angled line shows how C7724's sections rotate right (arrow) from the posterior midline.
B.
us
n
on
e
3
thm
O M B
al die n c
ph
Is
H
4
C R
Ve n tr
u m ellu eb er
Optic vesicle
eg
ct
m
T
Te
m
C E P H N E e n c e p hal o l Te
Side
l n N view rsa O Do phalo L n ce A n d ie
al
A.
MESENCEPH AL ON Pretectum
BRAINSTEM FLEXURES 1. Medullary 3. Mesencephalic 4. Diencephalic
Lower rhombic lip
SPINAL CORD
C.
Pretectum
Back view
Tectum
Left side -3.3º
Right side
e e b l l
e
u
r
PROSENOptic CEPHALON vesicle
Optic vesicle
C
m
R4 R5 R6
Medulla
R7
RHOMBENCEPHALON
Left side
Pons Rhombic lip border
Posterior midline
Medullary velum
Right side
-3.3º SPINAL CORD
Spinal cord
Scale bars = 0.25 mm
Medulla
PLATE 172A
Medullary velum
GW3.8 Sagittal, CR 3.5 mm, 24-25 somites, C7724 Level 1: Slide 2, Section 30
entricle protov le) h a lic tric
h ven c ep en e f o u r t m b fu tu r o ( rh
e cl ri
lic protov ha ep ture aqueduct ent c ) en (fu es m
Rathke's pouch epithelium (primordium of anterior pituitary gland)
Oral-pharyngeal cavity
Hyoid arch (II) Branchial preplacodes
Mandibular arch (I)
Lung bud?
diencephalic pool
Primordial mesenchymal brain case (skin, bone, and meninges)
prosencephalic protoventricle
8?
Cephalic preplacodes
Arterial trunk
telencephalic pool
APPROXIMATE MIDLINE AREA RIGHT SIDE OF BRAIN AND SPINAL CORD
Labeled on this page: Non-neural structures, brain ventricular divisions
Foregut/midgut
Liver?
LEFT SIDE OF BRAIN
12?
Um
Heart in pericardial swelling
bi
l ic
al
in ve
13
14 s)
Umbilical cord
num
ber
15
ate
16
Mesonephric vesicles
19 20
ral Ventrta ao
Notochord
See Plates 180A and B for a higher magnification view of the prosencephalon, mesencephalon, and anterior rhombencephalon in a nearyby section.
21
central canal
22 23? 24? MIDLINE
(app
18
Hindgut
roxim
17
Mesonephric duct
ites
THIS PORTION OF THE BODY CURVES TOWARD THE OBSERVER AND IS CUT IN THE CORONAL PLANE.
Som
372
Anterior somites 8-12 are indistinct and blend together. Somites 1-7 are not in this section.
Po nt
t
nc
ALON
tral die
al/isthm ent m g
V e p h a li c ?
Primordial gray matter
P
lenc
Primordial white matter
H
c
lic ha ep nc die
Te
en
N
O T e
AL
ephalic NE enc PSs s e M
h
P
p
al rs Do
Prosencephalic NEPS NEPs
Migrating spinal neurons
e
Te
te
Ascending fiber tracts Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP
al ic
re
Migrating vagal sensory (X) neurons from R7 NEP
Glial channels form superficial NEP border?
D C O R
al ct
te
A L
nt ra l
R2
I N
Sp Dor i n sal al te rm N e E di Ve a In
P
al
PLATE 172B
P
MESENCEPH
l
a
373
S
NCEPHALON RHOMBE Grac ile nucleand cu Upper rhombic lip IC NEPs L A ar N neate H P EP? E NC E N P y r a l l E u ed M B OM P R6 E RH R5 Lower R7 rhombic e N R4 n lip i R3
PROSEN
CE
Glial channels form superficial NEP border?
Brain surface (heavier line)
Labeled on this page: Central neural structures
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Spinal surface (heavier line)
Spinal NEP
Ventral Intermediate Dorsal
Arrows indicate the presumed direction of axon growth in brain fiber tracts. Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
GW3.8 Sagittal, CR 3.5 mm 24-25 somites, C7724 o v e n t Level 2: Slide 2, t r o i c l e (futu ic pr re Medullary velum hal fo p e u c RI Section 24 rt h ben M I D L INE
e cl ri
m
ve
nt
cl
diencephalic pool
Mandibular arch (I)
Cephalic preplacodes
Branchial preplacodes
Lung bud?
nk tru
prosencephalic protoventricle
ID
TS
F LE
diencephalic pool
(fu
en es m
AIN
Hyoid arch (II)
d or ch to
BR
Oral-p haryng eal cav ity
ial ter Ar
telencephalic pool?
e)
No
Rathke's pouch epithelium (primordium of anterior pituitary gland)
D NAL COR ND SPI IN A BRA OF DE SI
ri
)
rho
T H G
prot o alic ph re aqueduc ven e c tu t t
PLATE 173A
F EO
Liver?
Notochord
Foregut
Primordial mesenchymal brain case (skin, bone, and meninges)
Heart in pericardial swelling
ve in
Labeled on this page: Non-neural structures, brain ventricular divisions bi
lic
al
13? 14?
Um
Mid gut
Umbilical cord
15
16
19
Hindgut Notochord
a ort al a r t Ven
(a es it
22 23? 25?
24?
MID
E LIN
pp
21
m
See Plates 181A and B for a higher magnification view of the prosencephalon, mesencephalon, and anterior rhombencephalon in this section.
rox
20
central canal
te n umb
18
Mesonephric vesicle
ers)
17
Mesonephric duct
ima
THIS PORTION OF THE BODY CURVES TOWARD THE OBSERVER AND IS CUT IN THE CORONAL PLANE.
Dermatome Myotome
So
374
Sclerotome
375 RHOMBENC
EPHALON
on ti
ephalic N enc EP es Ss
l/is enta th gm e
ha
di
ep
al D o rs
ALON
PH
lic
nc
Glial channels form superficial NEP border?
Vent r a l die
M l Te
en
Primordial white matter
c ep
h a li c ?
PROS
EN
C
Spinal floor plate
Brain surface (heavier line)
Labeled on this page: Central neural structures Primordial white matter
PROPOSED RHOMBOMERE IDENTITIES R5 R6
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion.
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
Spinal surface (heavier line)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Spinal NEP Ventral
Intermediate Dorsal
C O R D
Prosencephalic NEPS NEPs
nc
lic ha ep
Spinal floor plate
E
th m al ?
Is
Pr
Glial channels form superficial NEP border?
al Dors a te m edi
Reticular, raphe, oculomotor (III), NEP? and red nuclear NEPs?
A L I N S P
Reticular, raphe, abducens (VI), and facial motor (VII) NEPs? NEP?
o e ypog lossator (X), an, l (XII) d NEPs ?
ra l Vent
tal l/tec cta e t e
P
mal
In te r
SENCEPHALO
Gra c N C E P H A L I C nucile an E N B lea d cu M E r N ne O EP ate P s? R H s Medullary N E P N E P ne Re R5 vaga ticular, ra R6 lm ph h
Cerebellar NEP?
l NEP Spina
ME
PLATE 173B
Lower rhombic lip
Te
N
Upper rhombic lip
PLATE 174A Primordial mesenchymal brain case (skin, bone, and meninges)
Medullary velum
rhom
GW3.8 Sagittal, CR 3.5 mm 24-25 somites, C7724 m ye len cep Level 3: Slide 2, hal ic p ool ic protoventricle l a h Section 20 (fu ep tu benc re
fo
ur
th
n
i
e)
AI BR OF
cl
DE
tr
SI
ve
FT LE
metencephalic pool
l- p h
a ry n
Hyoid arch (II)
g ea l
cavi
AL CORD SPIN ND NA
O ra
Rathke's pouch epithelium (primordium of anterior pituitary gland)
ty
Mandibular arch (I)
nk tru
Laryngotracheal groove?
M I D LINE
Cephalic preplacdes
central canal
(future aqueduct)
Branchial preplacdes
ial ter Ar
mesencephalic protoventricle
pr pr osen oto cep ven ha tri lic cle
Notochord
Um
bili cal vein
Labeled on this page: Non-neural structures, brain ventricular divisions
RIGHT S IDE
Heart in pericardial swelling
14? Midgut
15? 16?
Umbilical cord
17
Dermatome
Mesonephric duct
18
u m be rs)
19
THIS PORTION OF THE BODY CURVES TOWARD THE OBSERVER AND IS CUT IN THE CORONAL PLANE.
20
23? 25? 24?
MIDLINE
r ox i m
Som
See Plates 182A and B for a higher magnification view of the prosencephalon, mesencephalon, and anterior rhombencephalon in this section.
22
i tes
central canal
21
( ap p
Notochord
ate n
Hindgut Ve ao ntr rt al a
376
Myotome Sclerotome
R H O M B E N C E P H A L O
Upper rhombic lip
Cerebellar NEP
N
Po n ti n e R3 R2
Isthmal NEP
R4
R5
R6
Pioneer migrating hypothalamic, subthalamic, and tegmental neurons
ntal me eg
tal ec et
M B E N C E P H A L R H O I C M e d u llary EP
R7
PLATE 174B
N
N E NE P P
R va eticu hyp gal m lar, ra oglo otor phe ssa (X), , l (X II) Nand EPs ?
Lower rhombic lip
s
Glial channels form superficial NEP border?
ha
nc
NC
Primordial white matter
E
li c
ie Dorsal d
EPHALO
Pr
alic ep
Ve n t r a
l
di
en cep h
? c e p h a li c
PR
O
S
S P I N A L
T
en
Spinal NEP
Prosencephalic NEPS NEPs el
N
T
ENCEPHALO M E S alic N N EP ceph S n e s al Tect Me
Migrating isthmal neurons
377
Glial channels form superficial NEP border?
Ventral
Primordial gray matter
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
C O R D
Spinal floor plate
Dorsal
Labeled on this page: Central neural structures
Intermediate
Brain surface (heavier line)
Primordial white matter
Spinal surface (heavier line)
Spinal NEP
FONT KEY: Ventral ventricular divisions - capitals Germinal zone - Helvetica bold Intermediate Transient structure - Times bold italic Permanent structure - Times Roman or Bold Dorsal
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
PLATE 175A
GW3.8 Sagittal, CR 3.5 mm 24-25 somites, C7724 Level 4: Slide 2, LE FT Section 16 S
Medullary velum
le ntric otoicvlee) r p c i r phal h vent bence e fourt rhom (futur
ID E
F O
Oral-p haryng eal cav ity
Hyoid arch (II)
Mandibular arch (I)
Branchial preplacodes
ial ter ? Ar runk t
Cephalic preplacodes
Liver? Umbilical vein?
ce nt ra l
Labeled on this page: Non-neural structures, brain ventricular divisions
Midgut
Heart in pericardial swelling
ca na l
prosencephalic protoventricle (optic recess)
MIDLINE
Primordial mesenchymal brain case (skin, bone, and meninges)
D COR NAL SPI ND NA AI BR
Rathke's pouch epithelium (primordium of anterior pituitary gland)
Umbilical cord
Notochord
RIGHT SID E
17?
Mesonephric duct?
19
22
central canal
23?
THIS PORTION OF THE BODY CURVES TOWARD THE OBSERVER AND IS CUT IN THE CORONAL PLANE.
25?
24?
MIDLINE
ite s (
21
a p pro x i m ate
20
Som
Notochord
n u m be rs)
18
Ven tr a l ao r ta ?
378
Myotome and sclerotome Dermatome
ntal
e
e gm
ON
EPHAL
n
Migrating medullary (reticular formation?) neurons
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP Primordial gray matter
c germi
S
Tel
Prosencephalic NEPS
Spinal floor plate
R3 R4
R5
R6
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Ventral
PROPOSED RHOMBOMERE IDENTITIES
Dorsal
Intermediate
Labeled on this page: Central neural structures
R2
C O R D
N E P
O
p l a t e
E
h
Primordial white matter
NC
al
mi
cephalic? en
pt
PR
Brain surface (heavier line)
Migrating trigeminal neurons from R2 NEP
r o o f
O
Migrating vestibular and auditory neurons from R4 and R5 NEPs
S P I N A L
di D en or s a s c l e zone ph al al ic cephalic t r a l d i en Ve n
e Pr
t
? tal ec
Migrating hypothalamic, subthalamic, and tegmental neurons
T
Tectal?
Mesencephalic NEPS
Migrating vagal sensory (X) neurons from R7 NEP
i n a l S p
MES
PLATE 175B
S p i n a l
Migrating thalamic neurons?
379
P
I
ENCEPHALON
R H O M B E N C E P Migrating H A isthmal L O Upper rhombic lip neurons Dors Lower rhombic lip al lo N w er m B E N C E P H A M Cerebellar Trochlear Cerebellar O ed L ull nucleus (IV)? ("R1") NEP? NEP ary R H Medu I C NE l N P l a P E ry R6 R7 Ventr E N al low e P R5 N n i e t Po n R4 r me EP s al NEP dul R3 lary hm t R2 s NE
The dorsal lower medullary NEP contains cells that will expand later into a more defined mosaic including the cochlear nuclear NEP, the precerebellar NEP, and the gracile and cuneate nuclear NEPs.
Primordial white matter Primordial gray matter
The ventral lower medullary NEP contains cells that will expand later into a more defined mosaic including the following NEPs: raphe nuclear, vagal motor (X), hypoglossal (XII), prepositus nuclear, and reticular formation.
Spinal surface (heavier line)
Spinal NEP Ventral Intermediate Dorsal
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
PLATE ?A 176A
GW3.8 Sagittal, CR 3.5 mm GW3.5 24-25 somites, C7724 Level 5: Slide 2, LE FT Section 12 SI
velum llary Medu rh
om
b
entricle roticolev) lich p ntr phfa t ve r e u c e n re o t (fu
u
DE
O
F
B
R AI
N D AN
Branchial preplacodes
RD CO AL IN
Mandibular arch (I)
SP
Oral-pharyngeal cavity
Cephalic preplacodes
Arch III
Hyoid arch (II)
Optic vesicle ial ter k Ar run t
Primordial mesenchymal brain case (skin, bone, and meninges)
prosencephalic protoventricle (optic recess)
H
ea
Olfactory placode?
rt
in
pe
ri
Liver?
ca
rd
ia
ls
w
el
lin
Umbilical vein? MIDLINE
Midgut
g
RIGH T SI D
Labeled on this page: Peripheral neural and non-neural structures, brain ventricular divisions
E
Notochord
oxim ate n umb ers)
17?
18
central canal
24?
ite s (
22
THIS PORTION OF THE BODY CURVES TOWARD THE OBSERVER AND IS CUT IN THE CORONAL PLANE.
25?
21
INE DL MI
Som
Notochord
20
a p pr
r ta
19
Ven tr a l ao
380
Dermatome Myotome and sclerotome
R H O M B E N C E P Lower rhombic lip H
Upper rhombic lip
O M B E N C E P H A L R H I C M e d u
R2
EP
R4
R3
R5
R6
O
N
N E l l a r y P N E Dors al l o P wer me dul lar
s yN EP
Migrating medullary neurons
Migrating solitary nuclear neurons (IX glossopharyngeal receptors) from R6 NEP Migrating vestibular and auditory neurons from R4 and R5 NEPs
i
germ
mic al
Primordial gray matter
S P I N A L
Lateral prose cephalic NEP?
L
Migrating vagal sensory (X) neurons from R7 NEP
Brain surface (heavier line)
Glial channels form superficial NEP border?
R7
PLATE 176B
A
n a l S p i
g tin l ra ta ig ec ns M pret uro ne
Migrating trigeminal nuclear complex (V) neurons from R2 NEP Migrating facial (VII) neurons from R3 NEP
l zones
SENCEPH
Pon
N ti n e
na
g r a tin Migtectal s r on n eu
ME
Migrating isthmal neurons
l ma IsthEP? N
AL
O
N
Cerebellar NEP
381
t
h
O
SENCEPHA
L
Primordial white matter
Spinal roof
Labeled on this page: Central neural structures
R5
R6
R7
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Dorsal
R4
The optic vesicle is an evagination of the prosencephalon in the developing brain. It contains the opthalmic germinal zones, cells that will generate parts of the eye: retinal NEP, optic nerve glioepithelium, and the pigment epithelium.
plat e
R3
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Intermediate
R2
Spinal floor plate
Ventral
PROPOSED RHOMBOMERE IDENTITIES
C O R D
RO
N E P
P
N
Op
Primordial gray matter Primordial white matter
The dorsal lower medullary NEP contains cells that will expand later into a more defined mosaic including the cochlear nuclear NEP, the precerebellar NEP, and the gracile and cuneate nuclear NEPs. Spinal surface (heavier line)
Spinal NEP Ventral
Intermediate Dorsal
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Medullary velum
GW3.8 Sagittal, CR 3.5 mm GW3.5 24-25 somites, C7724 Level 6: Slide 2, Section 8
rhombencephalic protoventricle (future fourth ventricle)
BR AI N
PLATE 177A
LEFT SIDE OF
Formative cell-sparse superarachnoid reticulum
Oral cavity Oral-pharyngeal cavity
dis
tinc
Mandibular arch (I)
ite t som
Optic vesicle
Arch III
In
Hyoid arch (II)
s on left side of bod y
ial ter k Ar run t
Primordial mesenchymal brain case (skin, bone, and meninges)
prosencephalic protoventricle (optic recess)
Heart in pericardial swelling
Liver?
Labeled on this page: Non-neural structures, brain ventricular divisions
Umbilical vein?
MID LIN
See a high magnification view of the prosencephalon, mesencephalon, and rhombencephalon from the right side of the brain in Plates 184A and B.
E
central canal
THIS PORTION OF THE BODY FORMS A C-SHAPED CURVE, AND THE MIDLINE IS CUT IN TWO PLACES.
RIG
Notochord
HT SI
MIDLINE
P
24?
FS
ao r ta
DE O
25?
IN A L CO RD
central canal
Ve nt ra l
382
R H O M B E N C E P H A Lower rhombic lip L O M
Upper rhombic lip
EP P o n ti n e N
R2
Migrating isthmal neurons?
Neurons migrating from rhombomeres
R3
edulla ry N EP
R5
R4
383
PLATE 177B N
R6
Brain surface (heavier line)
R7
Trigeminal (V) Facial (VII) Vestibular and auditory (VIII)
Migrating medullary neurons
Glossopharyngeal receptors (IX) Vagal sensory (X)
Nerve X (vagus)? Cephalic preplacodes Glial channels form superficial germinal zone border? i
n
germ
zones
m
ic
al
PROSENCEPHALON
Branchial preplacodes
O pthal
Olfactory placode
Labeled on this page: Central and peripheral neural structures Primordial white matter
SPINAL CORD
R7
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
Sp
in
R6
P
R5
NE
R4
Spinal roof plate
al
R3
Intermediate
R2
The optic vesicle is an Trigeminal NEP - germinal source of the central trigeminal nuclei except the evagination of the prosencephalon in the mesencephalic nucleus. Facial NEP - germinal source of facial developing brain. It motor and sensory receptor neurons of contains the opthalmic germinal zones, cells Spinal floor plate the facial (VII) ganglion. that will generate parts of Vestibulo-auditory NEP - germinal the eye: retinal NEP, source (with R5) of central auditory nuclei and vestibular nuclei, except the optic nerve glioepithelium, and the cochlear nuclei. pigment epithelium. Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal Spinal floor plate source of the dorsal sensory nucleus and other sensory vagal nuclei.
Ventral
PROPOSED RHOMBOMERE IDENTITIES
Dorsal
Primordial gray matter
Primordial white matter Primordial gray matter
Spinal surface (heavier line)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Ventral Intermediate Dorsal
Spinal roof plate
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
384
PLATE 178A
GW3.8 Sagittal, CR 3.5 mm 24-25 somites, C7724 Level 7: Slide 1, Section 38 LE
1?
2?
FT
SI
DE
Arch III
Hyoid arch (II) Mandibular arch (I)
ter
io r
4? ca
Arch IV
rd
in
al
5?
ve in ?
DY BO
An
B
D AN
Oral-pharyngeal O ral cavity cavity
F
N AI R
3?
Superarachnoid reticulum
6?
Primordial mesenchymal brain case (skin, bone, and meninges)
7?
ial ter k Ar run t
8? 9?
H ea
prosencephalic protoventricle (optic recess)
O
rt in
10?
pe
11?
ri ca rd
12?
ia l
Labeled on this page: Non-neural structures, brain ventricular divisions
sw el
13?
li ng
14? 15?
Mesonephric vesicles
MID
LIN
E
16?
See a high magnification view of the prosencephalon, mesencephalon, and rhombencephalon from the right side of the brain in Plates 184A and B.
TS IDE RI
GH
ce nt ra lc an al
Posterior cardinal vein?
22?
21?
E IN DL I M
Somites (approximate numbers)
385
PLATE 178B
RHOMBENCEPHALON (lateral edge of pons) Nerve V boundary cap (Schwann cell GEP?) Lumen
Trigeminal ganglion (V) Vestibulocochlear ganglion (VIII) Migrating vestibulocochlear (VIII) ganglionic neurons from otic vesicle epithelium
zo
nes
ger min
Nerve X (vagus)?
Otic vesicle
Oral and pharyngeal preplacodes
Branchial preplacodes
al
PROSENCEPHALON (optic vesicle)
Germinal epithelium
Cephalic preplacodes
c
Optha l m i
Olfactory placode
Labeled on this page: Central and peripheral neural structures
The optic vesicle is an evagination of the prosencephalon in the developing brain. It contains the opthalmic germinal zones, cells that will generate parts of the eye: retinal NEP, optic nerve glioepithelium, and the pigment epithelium. The otic vesicle epithelium generates vestibular ganglionic neurons and spiral ganglionic neurons.
Primordial white matter
Spinal roof plate
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
al in
Do rsa l
NEP - Neuroepithelium
Sp
Spinal surface (heavier line)
NE
P
Ventral
Intermediate
Dorsal
Primordial gray matter
Spinal roof plate
SPINAL CORD
386
PLATE 179A
GW3.8 Sagittal, CR 3.5 mm 24-25 somites, C7724 Level 8: Slide 1, Section 30
LEFT SIDE OF BRAIN AND B ODY
1? A nt er io rc ar
2?
di na n? ei lv
Superarachnoid reticulum
3? 4?
Primordial mesenchymal brain case (skin, bone, and meninges)
5?
Somites (approximate numbers)
6?
prosencephalic protoventricle (optic recess)
7? Mandibular arch (I) Maxillary process
Hyoid arch (II)
Arch III
Arch IV
8?
ea
ial ter k Ar run t
H
9?
rt in pe
10?
ri ca rd
Labeled on this page: Non-neural structures, brain ventricular divisions
ia
11?
l sw el
12 (missing)?
li ng
13?
14?
15?
16?
Mesonephric vesicles
17? 18? 19?
THIS PORTION OF THE BODY IS CUT IN THE CORONAL PLANE.
20? 21? central canal
22? 24?
23? MIDLINE
Somites (approximate numbers)
387
PLATE 179B
Otic vesicle
Trigeminal ganglion (V)
Lumen
Facial ganglion (VII)
Germinal epithelium
Migrating Migrating facial facial ganglionic ganglion(VII) (VII) neurons from germinal source in placode?
Inferior glossopharyngeal ganglion (X) Glossopharyngeal placode?
Facial placode?
PROSENCEPHALON (optic vesicle)
At this level, branchial/pharyngeal placodes can be linked to presumptive sensory ganglia.
Vagal placodes?
Opthalmic germinal zones
Lens placode?
Inferior vagal ganglion (X) Cephalic and branchial placodes join (farther laterally, a similarly placed site is most likely the trigeminal placode) Olfactory placode
Labeled on this page: Central and peripheral neural structures The optic vesicle is an evagination of the prosencephalon. It contains the opthalmic germinal zones that will generate parts of the eye: retinal NEP, optic nerve glioepithelium, and the pigment epithelium. Some peripheral sensory neurons in the head are generated by the neural crest and some by the placodes. The olfactory placode generates primary olfactory sensory neurons (I). Branchial placodes on the pharyngeal arches generate some of the sensory neurons in the trigeminal ganglion (V), the facial ganglion (VII), the glossopharyngeal ganglia (IX), and the vagal ganglia (X). The otic vesicle epithelium generates some of the vestibular ganglionic neurons and spiral ganglionic neurons (both contribute axons to nerve VIII).
Spinal surface (heavier line) NEP - Neuroepithelium Arrows indicate the presumed direction of neuron migration from germinal sources.
Spinal NEP
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
SPINAL CORD (sacral tip)
This entire section is from the right side of the brain and body.
See Level 1 in Plates 172A and B.
GW3.8 Sagittal, CR 3.5 mm, C7724 Near Level 1: Slide 2, Section 33 PROSENCEPHALON, MESENCEPHALON, AND ANTERIOR RHOMBENCEPHALON
388
PLATE 180A
PLATE 180B
Brain surface (heavier line) Epithalamic
a Th
la m
ic
alic
pro
to
ve
nt
e
(f
ic
e
EP
H
R3
facial NEP
rhombencephalic protoventricle
(future fourth ventricle)
N
Pharyngeal preplacodes
Upper rhombic lip
AL O
Expanding superarachnoid reticulum
isthmal narrows canal
RHOMBEN C
R2
trigeminal NEP
NEP
Pros
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion.
Branchial preplacodes
Oral preplacodes
Pontin e
PROPOSED RHOMBOMERE IDENTITIES
r
Cerebellar NEP?
y p o t h ala m
Rathke's Rathke'spouch? pouch (primordium epitheliumof anterior (primordium pituitary of anterior gland) pituitary gland)
tu
ct)
o
Middl e/po ste rior h
u
du
rio r h y p
th
l
Mesenc ephal ic te gme nta lN EP
lic
Mesenceph ali c isthmal N EP
/a nte
Mandibular arch (I)
R3
cl
q
p ti c
ic m a la
tra
pha
Glial channels form superficial NEP border?
R2
ri
a
eo
n Ve
ce en di
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
ON
Me se nc ep ha
third ventricles)
ic thalam S ub
AL
ue
ephalic c n N e telencephalic pool E
mesenceph
diencephalic pool
prosencephalic prosencephalic protoventricle (future lateral and protoventricle
Pr
EPH
P NE al ct te
Telencephalic?
E PP
N NC
ENC
S
diencephalic pool
Cephalic preplacodes
MES
lic
PPRROOSSEE
P
phalic p retecta l NEP
n ai ) br es al ing ym en ch m en d es an m e, al on di b or in, im sk Pr se ( ca
H HA AL
LOO
N
N
M e s e n ce
phalic dience l a s r Do
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Medullary velum
389
LEFT SID EO FB R
GW3.8 Sagittal, CR 3.5 mm, C7724 Level 2: Slide 2, Section 24
N AI
PROSENCEPHALON, MESENCEPHALON, AND ANTERIOR RHOMBENCEPHALON
See Level 2 in Plates 173A and B.
IN L ID M
EA R EA
390
PLATE 181A
H
A
(future aqueduct)
(future lateral and third ventricles)
n
Mesencephalic tege men tal
ic i d d l e
r
s Po
Glial channels form superficial NEP border?
Upper rhombic lip
eN tin
EP
Reticular, raphe, abducens (VI), and facial motor (VII) NEPs?
rhombencephalic protoventricle
(future fourth ventricle) Medullary velum
CE
Branchial preplacodes
Medial po n
Oral-pharyngeal cavity
RHOM
Expanding superarachnoid reticulum
BE N
Rathke's pouch epithelium (primordium of anterior pituitary gland)
t
isthmal canal
? r NEP
Mandibular arch (I)
NEP)
er io
(hyp otha lam M
lla ebe Cer
alic
ON
ph
P
ce
NE P Reticular, raphe, oculomotor (III), and red nuclear NEPs?
diencephalic pool
Mesence ph al i c is th m
r
EP
prosencephalic protoventricle
e
P
e
en
rio
e p halic pre tecta l/te cta lN E
mesencephalic protoventricle
diencephalic pool
NC
NEP
Pr
te
Mes en c
NEP - Neuroepithelium
AL
telencephalic pool
h a li c N EP
SE
N
h a l i c NE
cep
ME
Isthmal
p ce
ie n
Brain surface (heavier line)
halamic Epit
O
Telencephalic N EP ?
ld
L
i ld ra n n t /a Ve optic
Cephalic preplacodes
Do rs a
PS
P ROSE
PS
ro s
NC
E
Thalamic
H
A
N
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
P
H
LO
Primordial mesenchymal brain case (skin, bone, and meninges)
G supe lial cha rfici nne al N ls fo r EP bordm er?
P NE al
PLATE 181B
391
GW3.8 Sagittal, CR 3.5 mm, C7724 Level 3: Slide 2, Section 20
PROSENCEPHALON, MESENCEPHALON, AND ANTERIOR RHOMBENCEPHALON LEFT SIDE OF BRAIN
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
See Level 3 in Plates 174A and B.
392
PLATE 182A
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
M
NEP - Neuroepithelium
P
?
ic
Pioneer migrating hypothalamic, subthalamic, tegmental and isthmal neurons
N
a
Expanding superarachnoid reticulum
d
Po ntine
R3
NEP
R4
Branchial preplacodes
a u (v e st d i t or ibulo yN EP )
Rathke's pouch epithelium (primordium of anterior pituitary gland)
(facialNEP)
Glial channels form superficial NEP border?
rhombencephalic protoventricle
h o t y p
Upper rhombic lip
(future fourth ventricle)
Te
r
MBENCEPHALON
lencephalic
lla
m
O AL
be
RHO
th
n
Mandibular arch (I)
re
P
ub
P)
a
Ce
R2
PROSENCEPH
mental
E i n al N
P r e o p t i c
Cephalic preplacodes
Te g
ma
(tr ig e m
h
Mese (future aqueduct) nce p h a li c NEPS
S
prosencephalic protoventricle
(future lateral and third ventricles)
mesencephalic protoventricle
u
P N E la a S
prosencephalic protoventricle
l
isth
E
sence p Pro h a l i c
cta
lic h a le ) ep tricuct c en en ed es v qu m otore a r p tu (f
mic Thala
te re
Migrating
Isthmal
Ep it
ic lam a h
N
Te c t a l
s ron eu ln
rm s fo er? nel bord n a P h al c NE Gli ficial r e sup
Primordial mesenchymal brain case (skin, bone, and meninges)
NCEPHALON ESE
e fa c sur line) n i Bra avier (h e
i c
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
l a m
PLATE 182B
Medullary velum
393
LATERAL MESENCEPHALON AND RHOMBENCEPHALON LEFT SIDE OF BRAIN See Level 5 in Plates 176A and B.
PROPOSED RHOMBOMERE IDENTITIES R2 R3 R4
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP - germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei.
R5 R6 R7
Vestibulo-auditory NEP - germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei Glossopharyngeal NEP - germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP - germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
394
GW3.8 Sagittal, CR 3.5 mm, C7724 Level 5: Slide 2, Section 12
PLATE 183A
PLATE 183B FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Early cell migration from rhombomeric NEPs
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
RHOMBENCEPHALON
NEP - Neuroepithelium
Lower rhombic lip
Primordial mesenchymal brain case (skin, bone, and meninges)
Upper rhombic lip
Cochlear nuclear NEP? Precerebellar NEP?
rhombencephalic protoventricle (future fourth ventricle)
Medullary NEP
Cerebellar NEP?
O
N
E ne N Ponti Isthmal NEP?
R2 (trigeminal NEP)
Brain surface (heavier line)
P
R4 (vestibuloauditory NEP)
R3 (facial NEP)
Migrating facial (VII) neurons from R3 NEP Migrating trigeminal nuclear complex (V) neurons from R2 NEP
g ra tin M ig cta l te n s ro neu
MESENCE
PH
AL
Migrating isthmal neurons
Gracile and cuneate nuclear NEP?
R5 (vestibuloauditory NEP)
R7 (vagal NEP)
R6 (glossopharyngeal NEP)
Dorsal lower medullary NEP
Migrating vestibular and auditory (VIII) neurons Migrating solitary nucleus neurons from R4 and R5 NEPs (IX, glossopharyngeal receptors) from R6 NEP Migrating vagal sensory (X) neurons from R7 NEP
Expanding superarachnoid reticulum
Oral preplacodes
Oral-pharyngeal cavity
Migrating medullary neurons
Branchial preplacodes
ng ati al igr ct s M rete ron p eu n
Cephalic preplacodes Hyoid arch (II)
Arch III
Pharyngeal preplacodes
Mandibular arch (I)
395
GW3.8 Sagittal, CR 3.5 mm, C7724 Similar to Levels 6 and 7 on the right side of brain: Slide 2, Section 42 LATERAL PROSENCEPHALON, MESENCEPHALON, AND RHOMBENCEPHALON
PROPOSED RHOMBOMERE IDENTITIES R2 R3
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion.
See Level 6 in Plates 177A and B, Level 7 in Plates 178A and B.
396
PLATE 184A
PLATE 184B Brain surface (heavier line)
NEP - Neuroepithelium FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
RHOM BEN CEP HA LO N
Arrows indicate the presumed direction of neuron migration from neuroepithelial sources.
Pontine NEP
Lumen
Migrating trigeminal nuclear complex (V) neurons from R2 NEP
Migrating tegmental neurons
li u m
Migrating facial (VII) neurons from R3 NEP
Nerve IX (glossopharyngeal)?
th e
Migrating isthmal neurons
Otic vesicle
R3 (facial NEP)
pi
ct)
Te g m e n t a l N E P
l N EP
Te c t a
me pr sence (fu otove phal tur e aqntric ic ued le u
Isthmal NEP?
R2 (trigeminal NEP)
G er min a
le
Vestibulocochlear ganglion (VIII)
Nerve X (vagus)? Migrating vestibulocochlear ganglionic neurons (VIII) from otic vesicle epithelium
tal NEP
Migrating te
MESENCEP
HAL
ON
ctal n eur on s?
Isthmal NEP?
ec Pret
Expanding superarachnoid reticulum
Cephalic preplacodes Oral preplacodes
Oral-pharyngeal cavity Migrating pretectal neurons
Opthalmic germinal zones
Branchial preplacodes Glial channels form superficial germinal zone border?
prosencephalic protoventricle (optic recess)
Primordial mesenchymal brain case (skin, bone, and meninges)
Mandibular arch (I)
Hyoid arch (II)
Arch III Arch IV
397
Optic vesicle PROSENCEPHALON
Pharyngeal preplacodes
398
PART PARTXV: XV: GW3.2 GW3.2 CORONAL CORONAL
This specimen is embryo #714 in the Minot Collection, designated here as M714. The crown-rump length (CR) is 4-mm. CR length is an unreliable measure to estimate gestational age because this specimen is much less mature than C7724, which also has a 4-mm CR. Since the number of somites could not be counted accurately in transverse sections, age determination is based on the degree of maturation of the central nervous system. The anterior neuropore closes at the 20-somite stage (Patten, 1953; Hamilton et al., 1959); M714 has a large open anterior neuropore. Using the timetables in Patten (1953) and Hamilton et al. (1959), we estimate that M714 has approximately 17 to 18 somites and is at gestational week (GW) 3.2. M714’s prosencephalic and anterior mesencephalic sections are cut (8 µm) in the coronal plane, but the plane shifts to predominantly horizontal in the posterior mesencephalon, pons, and medulla. We photographed 21 sections at low magnification from the first section containing the head to the posterior tips of the rhombencephalon. Fifteen of these sections are illustrated in Plates 185AB to 197AB. All photographs were used to produce computer-aided 3-D reconstructions of the external features of M714’s brain and optic vesicle (Figure 14), and to show each illustrated section in situ (insets, Plates 185A to 197A). Each illustrated section shows the brain with all surrounding tissues. Labels in A Plates (normal-contrast images) identify nonneural and peripheral neural structures; labels in B Plates (low-contrast images) identify central neural structures. The prosencephalon is small and incomplete with a slit-like protoventricle. In front of the optic vesicles, the anterior neuropore is broadly open ventrally, and narrows dorsally. The most anterior sections have a continuum between the neuroepithelium (presumptively future telencephalic) and the cephalic preplacodal epithelium. The dorsal part of the anterior neuropore is closed in sections of the optic vesicle; these neuroepithelia are more clearly
identified as future diencephalic. The preplacodal epithelium lines the lateral and ventral surfaces of the head and roof of the oral cavity. The evaginated optic vesicle is nearly touching part of the preplacodal epithelium that may have something to do with induction of the lens placode later on. An olfactory placode is very difficult to identify. The mesencephalon contains a stockbuilding neuroepithelium surrounding a narrow keyhole-shaped protoventricle. Future tectal neuroepithelium is a small arch over the top, while the future tegmental and isthmal neuroepithelia form the slite-shaped bottom. There is a very thin cell-free primordial plexiform layer in future tegmental and isthmal areas. The most prominent neuroepithelial structures in the rhombencephalon are the rhombomeric evaginations. In this specimen, several sections show how closely rhombomeres are associated with sensory cranial ganglia. The trigeminal ganglion (source of V sensory axons) is nearly attached to the brain surface at rhombomere 2. The vestibulocochlear ganglion (source of VIII axons) is attached to the rhombomere 4 brain surface. The otic vesicle touches the rhombomere 5 brain surface. The presumptive glossopharyngeal ganglion (source of IX sensory axons) is lateral to rhombomere 6. The short nerve extending from the large vagal ganglion (source of X sensory axons) touches the rhombomere 7 brain surface. The presumptive facial ganglion (source of sensory VII axons) is near a placode in the hyoid arch, slightly posterior and ventrolateral to rhombomere 3. A very thin layer of migrating neurons lines the superficial border of some rhombomeres; for the most part, cell migration has not yet started. The small cerebellar neuroepithelium is barely identifiable in the most posterior sections where the dorsal rhombencephalic neuroepithelium blends with tectal/isthmal neuroepithelia.
399
M714 Computer-aided 3-D Brain Reconstructions MESE NC A. Angled front view B. Side view
P o n
s
Open anterior neuropore
Preoptic area Hypothalamus
Preoptic area Infundibulum Mammillary body
R3
R4+5
Upper medulla
RHOMBENCEPHALON
R6+7
Medullary velum
R2
BRAINSTEM FLEXURES
R4+5
R6+7
Lower medulla
Lower medulla
Cerebellum
R3
edulla Upper m
Ventral diencephalon
R2
3
H y p ot
RHOMBENCEPHALO N
Future telencephalon?
Future telencephalon?
m
P o n s
Cerebellum
Optic vesicle
Optic vesicle
tu en
S u bthalamus Te g m la mu s
Teg me nt u
m
Upper rhombic lip
4
ha
Subthalamus
Thalamus
PROSENCEPHALON
Thalamus
Epithalamus
N
Epithalamus
Isthmus
Dorsal diencephalon
Isthmus
PROSENCEPHALON
Tectum
LO
M E S E N C E P H Pretectum A Tectum
EP H A L O N
Pretectum
1. Medullary 3. Mesencephalic
1
4. Diencephalic
Lower rhombic lip
R - Rhombomere Spinal cord Spinal cord
C. Top view
C
s
w
p
RHOMBENCEPHALON
d
nal Cor pi
a ll
me d er u
P s n o
R6+7
la
med er u
l
o
u m h t
Te
s
u gm e nt
u
s us
am
y
H
la m
I
tha
P
Scale bars = 0.25 mm
po
s
p
Roof of diencephalic protoventricle
Sub
th
al
n
U
m
Future telencephalon?
ea c ar pti eo Pr
PROSENCEPHALON
s
R4+5
o
Open anterior neuropore
R3
L
R2
MESENCEPHALON
Optic vesicle
S
D. Bottom view
r C o
T
h m e r e u b e l l
m
e
Pr
c
t
u
etectum
Epithalamus
a lamu
Th
s
u
s
m
s
I
Medullary velum
i n a l
Upper rhombic lip
t
Figure 14. A, The left side of the 3–D model viewed from the front at a 45º heading; this view is used to "peel away" sections of each level in the following Plates. B, A straight view of the left side. C, A straight down view of the top. D, An upward view of the bottom, angled (120º) to look into the mesencephalic and diencephalic flexures. Arrows indicate the open anterior neuropore.
RHOMBENCEPHALON
Future telencephalon? Open anterior neuropore
n P o
PROSENCEPHALON
R2
d
MESENCEPHALON
Optic vesicle
S
p
400
PLATE 185A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714
Level 1: Section 3 Primordial mesenchymal brain case (skin, bone, and meninges)
Dorsal junction between cephalic preplacodal epithelium and prosencephalic NEP
Cephalic preplacode
Level 1: Computer-aided 3-D Brain Reconstruction
Ventral junction between cephalic preplacodal epithelium and prosencephalic NEP
Level 2: Section 13 Cephalic preplacode
Optic vesicle
Lens placode?
Level 2: Computer-aided 3-D Brain Reconstruction
Future olfactory placode? Ventral junction between cephalic preplacodal epithelium and prosencephalic NEP
Primordial mesenchymal brain case (skin, bone, and meninges)
401
PLATE 185B
Central neural structures labeled
PROSENCEPHALON
Level 1: Section 3 closing anterior neuropore (dorsal) Brain surface (heavier line)
Prosencephalic NEP
(future diencephalic?)
Prosencephalic primordial plexiform layer
open prosencephalic protoventricle
Prosencephalic NEP
(future lateral and third ventricles)
(future telencephalic?)
anterior neuropore (ventral)
Level 2: Section 13
PROSENCEPHALON THALAMUS
Diencephalic roof plate
(future choroid plexus in roof of third ventricle)
Thalamic NEP
Thalamic primordial plexiform layer Brain surface (heavier line)
SUBTHALAMUS
Subthalamic NEP
Subthalamic primordial plexiform layer
Anterior hypothalamic NEP?
Hypothalamic primordial plexiform layer?
Future pigment epithelium?
Optic vesicle
diencephalic protoventricle
Future retinal NEP?
(future third ventricle) optic recess Preoptic primordial plexiform layer?
Preoptic area NEP? VENTRAL DIENCEPHALON
open prosencephalic protoventricle (future lateral and third ventricles)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
closing anterior neuropore (ventral)
NEP - neuroepithelium
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
402
PLATE 186A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 3: Section 18
Primordial mesenchymal brain case (skin, bone, and meninges)
Optic vesicle
Cephalic preplacode
Future lens placode?
Future olfactory placode?
Branchial preplacode
Lateral tongue primordium?
Mandibular arch (I)
The GW4 Face and Neck
Figure 247A modified (Patten, 1953, p. 429.)
Frontal prominence Optic vesicle Olfactory placode Future oral cavity Tongue and mandible primordia
Maxillary process Mandibular arch (I)
Hyo-mandibular cleft Hyoid arch (II)
Level 3: Computer-aided 3-D Brain Reconstruction
Arches III and IV
403
PLATE 186B
Central neural structures labeled
DIENCEPHALON THALAMUS/EPITHALAMUS
Diencephalic roof plate
(pineal gland primordium?)
Epihalamic NEP?
Thalamic/epithalamic primordial plexiform layer Brain surface (heavier line)
Thalamic NEP? SUBTHALAMUS
Subthalamic NEP
Subthalamic primordial plexiform layer
Middle hypothalamic NEP?
Hypothalamic primordial plexiform layer
Future pigment epithelium?
optic recess
Optic vesicle Future retinal NEP?
Hypothalamic primordial plexiform layer
Anterior hypothalamic NEP?
Preoptic primordial plexiform layer
Preoptic area NEP? Diencephalic floor plate VENTRAL DIENCEPHALON
diencephalic protoventricle
(future third ventricle)
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - neuroepithelium
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
404
PLATE 187A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 4: Section 28
Primordial mesenchymal brain case (skin, bone, and meninges) Maxillary process Optic vesicle Cephalic preplacode Cephalic preplacode Future Rathke's pouch?
Branchial preplacodes
Lateral tongue primordium Part of the mandibular arch placodal epithelium gives rise to the thyroid gland.
Arterial trunk Peritoneal cavity
Level 4: Computer-aided 3-D Brain Reconstruction
Mandibular arch (I)
405
PLATE 187B
Central neural structures labeled
DIENCEPHALON THALAMUS/EPITHALAMUS
Diencephalic roof plate Epihalamic NEP?
Thalamic/epithalamic primordial plexiform layer Brain surface (heavier line)
Thalamic NEP SUBTHALAMUS Subthalamic primordial plexiform layer
Subthalamic NEP
diencephalic protoventricle
Optic vesicle germinal zone
(future third ventricle)
infundibular recess
Hypothalamic NEP
Diencephalic floor plate
Hypothalamic primordial plexiform layer
(primordium of median eminence and neurohypophysis?)
VENTRAL DIENCEPHALON
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
NEP - neuroepithelium
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
406
PLATE 188A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 5: Section 33 Primordial mesenchymal brain case (skin, bone, and meninges)
Sphenoid primordium?
Posterior optic vesicle? Maxillary process Cephalic preplacode Trigeminal ganglion placode?
Future Rathke's pouch? Lateral tongue primordium Branchial/pharyngeal preplacodes
Mandibular arch (I)
Part of the mandibular arch placodal epithelium gives rise to the thyroid gland. Hyoid arch (II)
Medial tongue primordia Arterial trunk
Arch III?
Peritoneal cavity
Primitive gut
Level 5: Computer-aided 3-D Brain Reconstruction
407
PLATE 188B
Central neural structures labeled DIENCEPHALON THALAMUS/EPITHALAMUS
Diencephalic roof plate Epihalamic NEP
Thalamic/epithalamic primordial plexiform layer Brain surface (heavier line)
Thalamic NEP SUBTHALAMUS Subthalamic primordial plexiform layer
Subthalamic NEP
diencephalic protoventricle
(future third ventricle) Hypothalamic primordial plexiform layer
Middle/posterior hypothalamic NEP?
infundibular and mammillary recesses
Diencephalic floor plate
(primordium of median eminence and neurohypophysis?)
Migrating trigeminal ganglionic (V) neurons?
Peripheral neural structure
HYPOTHALAMUS
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from germinal sources.
NEP - neuroepithelium
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
408
Peripheral neural and non-neural structures labeled
PLATE 189A GW3.2 Coronal 17-18 Somites? M714 Level 6: Section 38 Primordial mesenchymal brain case (skin, bone, and meninges)
Sphenoid primordium?
Cephalic preplacode
Trigeminal ganglion (V) placode? Branchial/pharyngeal preplacodes
Rathke's pouch epithelium (primordium of anterior pituitary) Oralpharyngeal cavity
Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Maxillary process
Mandibular arch (I)
Hyoid arch (II)
Arch III?
Arterial trunk
Arch IV?
Peritoneal cavity
Primitive gut
Level 6: Computer-aided 3-D Brain Reconstruction
409
PLATE 189B
Central neural structures labeled MESENCEPHALON PRETECTUM
Mesencephalic roof plate
mesencephalic protoventricle (future aqueduct)
Pretectal primordial plexiform layer
Pretectal NEP
Brain surface (heavier line)
SUBTHALAMUS?
Subthalamic NEP
Subthalamic primordial plexiform layer
diencephalic protoventricle
(future third ventricle) Hypothalamic primordial plexiform layer
Posterior hypothalamic NEP
mammillary recess
Peripheral neural structure
Diencephalic floor plate
Migrating trigeminal ganglionic neurons from the trigeminal placode in the fusing maxillary process and mandibular arch
HYPOTHALAMUS
DIENCEPHALON
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Arrows indicate the presumed direction of neuron migration from germinal sources.
NEP - neuroepithelium
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
PLATE 190A GW3.2 Coronal 17-18 Somites? M714 Level 7: Section 43
achnoid reticulum
Peripheral neural and non-neural structures labeled
Sphenoid primordium?
ativ e su
per a r
Primordial mesenchymal brain case (skin, bone, and meninges)
For m
410
Cephalic preplacode
Migrating trigeminal ganglionic neurons? Trigeminal ganglion (V) placode? Branchial/pharyngeal preplacodes
Maxillary process
Rathke's pouch epithelium (primordium of anterior pituitary)
Oral-pharyngeal cavity
Mandibular arch (I)
Hyoid arch (II) Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Arch III?
Anterior cardinal vein?
Arch IV? Primitive gut
Ganglion X?
Anterior cardinal vein Dorsal aorta Notochord Dorsal root ganglion
Level 7: Computer-aided 3-D Brain Reconstruction
Somites
411
Central neural structures labeled MESENCEPHALON
PLATE 190B Pretectal primordial plexiform layer
PRETECTUM
Mesencephalic roof plate Pretectal NEP
TEGMENTUM
Brain surface (heavier line) Tegmental primordial plexiform layer
Tegmental NEP
mesencephalic protoventricle
Diencephalic floor plate
(future aqueduct)
Hypothalamic primordial plexiform layer
Posterior hypothalamic NEP
Future mammillary body
HYPOTHALAMUS
DIENCEPHALON
Peripheral neural structure Migrating trigeminal ganglionic neurons from the trigeminal placode in the fusing maxillary process and mandibular arch
SPINAL CORD
Arrows indicate the presumed direction of neuron migration from germinal sources.
Spinal germinal zones
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
Spinal floor plate
(ventral commissural GEP)
Ventral NEP
Primordial white matter
Intermediate NEP Dorsal NEP Spinal roof plate
slit-shaped central canal
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 8: Section 58
achnoid reticulum
PLATE 191A
per a r
Primordial mesenchymal brain case (skin, bone, and meninges)
ativ e su
Fused maxillary process and mandibular arch (I)
For m
412
Trigeminal ganglion (V) Trigeminal ganglion (V) placode?
Anterior cardinal vein? Maxillary process
Notochord
Migrating trigeminal ganglionic neurons? Trigeminal ganglion (V) placode?
Internal carotid artery?
Mandibular arch (I)
Pharynx Hyoid arch (II) Multiple loci in the placodal epithelium of the arches gives rise to the thyroid, parathyroid, and thymus glands.
Vagal ganglion (X) placode? Migrating vagal ganglionic (X) neurons?
Branchial/ pharyngeal preplacodes
Arch III?
Arch IV?
Vagal ganglion (X)? Anterior cardinal vein Dorsal aorta
Notochord
Somites Dorsal root ganglion primordium
Level 8: Computer-aided 3-D Brain Reconstruction
Central neural structures labeled MESENCEPHALON TECTUM
Mesencephalic roof plate Tectal NEP
TEGMENTUM
Tegmental NEP
413
Tectal primordial plexiform layer
PLATE 191B
Brain surface (heavier line)
mesencephalic protoventricle (future aqueduct)
Tegmental primordial plexiform layer
Mesencephalic floor plate
Peripheral neural structures
Migrating trigeminal ganglionic neurons from the trigeminal placode in the fused maxillary process and mandibular arch
Migrating vagal ganglionic neurons from the vagal placode in arch IV
SPINAL CORD
Spinal germinal zones Spinal floor plate
(ventral commissural GEP)
Ventral NEP Intermediate NEP Dorsal NEP Spinal roof plate
Primordial white matter
slit-shaped central canal
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells. ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
PLATE 192A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 9: Section 63
achnoid reticulum
Primordial mesenchymal brain case (skin, bone, and meninges)
ativ e su
per a r
Fused maxillary process and mandibular arch (I)
For m
414
Trigeminal ganglion (V)
Anterior cardinal vein?
Notochord Internal carotid artery? Facial ganglion (VII) placode?
Hyoid arch (II)
Facial ganglion VII?
Glossopharyngeal ganglion IX? Glossopharyngeal ganglion (IX) placode? Arch III?
Dorsal aorta Pharyngeal preplacodes
Pharynx
Vagal ganglion (X) placode?
Arch IV?
Vagal ganglion (X)?
Anterior cardinal vein?
Notochord
Somites Dorsal root ganglion
Level 9: Computer-aided 3-D Brain Reconstruction
415
Central neural structures labeled Tectal primordial plexiform layer
MESENCEPHALON TECTUM
Mesencephalic roof plate
PLATE 192B
Brain surface (heavier line)
Tectal NEP TEGMENTUM/ISTHMUS
Tegmental NEP Mesencephalic floor plate
mesencephalic protoventricle
(future aqueduct)
Tegmental primordial plexiform layer
(raphe glial system GEP)
Isthmal NEP
Metencephalic floor plate
Peripheral neural structures
(raphe glial system GEP)
PONS
Migrating trigeminal ganglionic neurons from the trigeminal placode in the fused maxillary process and mandibular arch
RHOMBENCEPHALON
Migrating facial ganglionic neurons from the facial placode in the hyoid arch Migrating glossopharyngeal ganglionic neurons from the glossopharyngeal placode in arch III
Migrating vagal ganglionic neurons from the vagal placode in arch IV
SPINAL CORD
Spinal germinal zones Spinal floor plate
(ventral commissural GEP)
Ventral NEP
Intermediate NEP Dorsal NEP Spinal roof plate
Primordial white matter
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
ABBREVIATIONS: slit-shaped GEP - Glioepithelium central NEP - Neuroepithelium canal FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
416
PLATE 193A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 10: Section 68
Facial ganglion (VII) placode? Facial ganglion (VII)?
Glossopharyngeal ganglion (IX)? Glossopharyngeal ganglion (IX) placode? Notochord Vagal ganglion X?
Anterior cardinal vein?
s u p e r a r a c h n o i d
Trigeminal ganglion (V)
F o r m a t i v e
Fused maxillary process and mandibular arch
r e t i c u l u m
Primordial mesenchymal brain case (skin, bone, and meninges)
Ganglion VIII
Hyoid arch (II)
Arch III?
Arch IV?
Somites Dorsal root ganglion primordium
Dorsal root ganglion boundary cap (Schwann cell GEP?)
Level 10: Computer-aided 3-D Brain Reconstruction
417
PLATE 193B
Central neural structures labeled Brain surface (heavier line)
MESENCEPHALON TECTUM
Mesencephalic roof plate Tectal NEP
Tectal primordial plexiform layer
TEGMENTUM/ISTHMUS
Tegmental NEP
Isthmal NEP
Tegmental primordial plexiform layer
Isthmal primordial plexiform layer
mesencephalic protoventricle
(future aqueduct)
Medial pontine NEP Metencephalic floor plate
(midline raphe glial system GEP) Pontine primordial plexiform layer
PONS
Medial pontine NEP
Peripheral neural structures
RHOMBENCEPHALON
Migrating glossopharyngeal ganglionic neurons from the glossopharyngeal placode in arch III
Peripheral neural structure Migrating facial ganglionic neurons from the facial placode in the hyoid arch
Migrating vagal ganglionic neurons from the vagal placode in arch IV
SPINAL CORD
Spinal germinal zones Spinal floor plate
(ventral commissural GEP)
Ventral NEP
Ventral commissure
Primordial white matter
Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
Intermediate NEP
Dorsal NEP Spinal roof plate
Arrows indicate the presumed direction of neuron migration from germinal sources.
slit-shaped central canal
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
418
PLATE 194A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 11: Section 73
Primordial mesenchymal brain case (skin, bone, and meninges)
Fused maxillary process and mandibular arch Trigeminal ganglion (V) Trigeminal ganglion boundary cap (Schwann cell GEP?)
Vestibulocochlear ganglion (VIII) Epithelium Lumen
Glossopharyngeal ganglion (IX)?
Anterior cardinal vein?
Vagal ganglion (X)?
Formative iculum superarachn oid ret
Otic vesicle
Somites
Dorsal root ganglion boundary cap (Schwann cell GEP?)
Level 11: Computer-aided 3-D Brain Reconstruction
419
Central neural structures labeled MESENCEPHALON ISTHMUS
PLATE 194B PROPOSED RHOMBOMERE IDENTITIES
Brain surface (heavier line)
Mesencephalic roof plate
R2 Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R3 Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. R4 Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R5 Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R6 Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. R7 Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Isthmal primordial plexiform layer
Isthmal NEP mesencephalic protoventricle
(future aqueduct)
PONS/MEDULLA
rhombencephalic protoventricle
(future fourth ventricle)
Medial pontine NEP Migrating trigeminal (V) neurons?
R2 (trigeminal NEP) Migrating facial (VII) neurons R3 (facial NEP)
R4+5 (vestibulo-auditory NEP)
Migrating vestibulocochlear ganglionic neurons from the otic epithelium
Migrating vestibulo-auditory (VIII) neurons
R6 (glossopharyngeal NEP)
Peripheral neural structure
Migrating glossopharyngeal receptor neurons (solitary nucleus)
R7 (vagal sensory NEP) Migrating vagal sensory (X) neurons Migrating vagal motor (X) and hypoglossal (XII) neurons?
Medial medullary NEP
(vagal motor [X] and hypoglossal [XII] NEPs blend with ventral spinal NEP)
RHOMBENCEPHALON SPINAL CORD
Spinal germinal zones Ventral NEP
Migrating ventral gray neurons? Primordial white matter
Intermediate NEP
Dorsal NEP Spinal roof plate
Migrating intermediate gray neurons?
slit-shaped central canal
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
420
PLATE 195A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 12: Section 78
Primordial mesenchymal brain case (skin, bone, and meninges)
Vestibulocochlear ganglion (VIII)
Otic placode Otic vesicle
Epithelium Lumen
Glossopharyngeal ganglion (IX)
Vagal ganglion (X)
Somites
Dorsal root ganglion boundary cap (Schwann cell GEP?)
Level 12: Computer-aided 3-D Brain Reconstruction
421
PLATE 195B
Central neural structures labeled
PROPOSED RHOMBOMERE IDENTITIES
MESENCEPHALON ISTHMUS
R2 Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. R3 Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. R4 Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R5 Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R6 Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. R7 Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Brain surface (heavier line)
Mesencephalic roof plate Isthmal primordial plexiform layer
Isthmal NEP mesencephalic protoventricle
(future aqueduct)
PONS/MEDULLA
R2 (trigeminal NEP) rhombencephalic protoventricle R3 (facial NEP)
(future fourth ventricle)
R4 (vestibulo-auditory NEP) Migrating vestibulo-auditory neurons
Migrating vestibulocochlear ganglionic neurons from the otic epithelium
R5 (vestibulo-auditory NEP)
Peripheral neural structure
Migrating glossopharyngeal receptor neurons (solitary nucleus) R6 (glossopharyngeal NEP)
R7 (vagal sensory NEP)
Migrating vagal sensory (X) neurons
Intermediate medullary NEP
(blends with intermediate spinal NEP)
Pioneer migrating medullary and spinal neurons
RHOMBENCEPHALON SPINAL CORD
Spinal germinal zones
Intermediate NEP
Primordial white matter
Dorsal NEP Spinal roof plate
slit-shaped central canal
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
422
PLATE 196A
Peripheral neural and non-neural structures labeled
GW3.2 Coronal 17-18 Somites? M714 Level 13: Section 83
Primordial mesenchymal brain case (skin, bone, and meninges)
Vestibulocochlear ganglion (VIII) Migrating vestibulocochlear ganglionic neurons from the otic epithelium Epithelium
Otic vesicle
Lumen
Glossopharyngeal ganglion boundary cap* Glossopharyngeal ganglion (IX) Vagal ganglion (X)
Vagal ganglion boundary cap*
Dorsal root ganglion boundary caps*
* Boundary caps are
Schwann cell GEPs? Somites
Level 13: Computer-aided 3-D Brain Reconstruction
423
PLATE 196B
Central neural structures labeled
Brain surface (heavier line)
Midline rhombencephalic roof plate CEREBELLUM
Cerebellar NEP (vermis?)
Fibrous layer in superficial cerebellum
Cerebellar NEP (hemisphere?) rhombencephalic protoventricle
(future fourth ventricle)
Lateral rhombencephalic roof plate? PONS/MEDULLA
(future rhombic lips)
R3 (facial NEP)
metencephalic pool
PROPOSED RHOMBOMERE IDENTITIES
Future medullary velum
R3 Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. R4 Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R5 Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. R6 Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. R7 Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Migrating vestibulo-auditory neurons
R4 (vestibulo-auditory NEP)
myelencephalic pool
R5 (vestibulo-auditory NEP) Migrating glossopharyngeal receptor neurons (solitary nucleus) R6 (glossopharyngeal NEP)
R7 (vagal sensory NEP) Migrating vagal sensory (X) neurons
Dorsomedial lower medullary NEP
(blends with dorsal spinal NEP)
RHOMBENCEPHALON SPINAL CORD
Pioneer migrating medullary and spinal neurons
Spinal germinal zones Dorsal NEP
Primordial white matter
slit-shaped central canal
Spinal roof plate
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium R - Rhombomere Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells.
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
424
PLATE 197A GW3.2 Coronal 17-18 Somites? M714
Peripheral neural and non-neural structures labeled
Level 14: Section 88
Primordial mesenchymal brain case (skin, bone, and meninges)
Level 14: Computer-aided 3-D Brain Reconstruction
Level 15: Section 93
Level 15: Computer-aided 3-D Brain Reconstruction
Primordial mesenchymal brain case (skin, bone, and meninges)
Central neural structures labeled
425 Anteromedial myelencephalic roof plate
PLATE 197B
Level 14: Section 88
MEDULLA Lateral myelencephalic roof plate (ventral rhombic lip)
Medullary velum
Future precerebellar and auditory
(cochlear nuclear)
NEPs?
rhombencephalic protoventricle
(future fourth ventricle, myelencephalic pool)
Dorsomedial lower medullary NEP (gracile and cuneate nuclei?)
Migrating gracile and cuneate nuclear neurons?
Level 15: Section 93 Posteromedial myelencephalic roof plate
MEDULLA
Anteromedial myelencephalic roof plate
RHOMBENCEPHALON Medullary velum
Dorsomedial lower medullary NEP (gracile and cuneate nuclei?)
NEP - neuroepithelium
rhombencephalic protoventricle
Arrows indicate the presumed direction of neuron migration from germinal sources. Arrows indicate the regionally expanding shoreline of the protoventricle with increase in stockbuilding NEP cells. FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Migrating gracile and cuneate nuclear neurons?
(future fourth ventricle, myelencephalic pool) Posteromedial myelencephalic roof plate
RHOMBENCEPHALON
426
PART PARTXVI XVI
CONCLUDING CONCLUDING ESSAY ESSAY JOSEPH ALTMAN and SHIRLEY A. BAYER
We began to work on this project over a decade ago to produce a comprehensive, multi-volume Atlas of Human Central Nervous System Development (CNS). Our aim in starting this project was to try to interpret normal human CNS development in light of the understanding we have gained in the preceding three decades from an experimental analysis of the prenatal and postnatal development of the rat CNS. In that extensive work, we injected 3H-thymidine at daily intervals to groups of pregnant rats. Those injections labeled DNA in the proliferating progenitors of neurons and neuroglia in the rat embryos and fetuses. We also injected 3H-thymidine at varied intervals to groups of infant, juvenile, and adult rats to study the postnatal course of cell proliferation during late CNS development. By varying survival times after administration of the radiochemical from hours, to days and months, we used the techniques of short-survival, sequential-survival, and long-survival autoradiography to achieve the following. (1) Determine the proliferation dynamics of progenitor cells in the various compartments (mosaics) of the primary neuroepithelium (NEP) and in the various secondary germinal matrices—cortical and striatal subventricular zones (SVZ), cerebellar external germinal layer (EGL), hippocampal subgranular zone (SGZ)—as a function of prenatal and postnatal age. (2) Track the migratory routes of different populations of young neurons, their sojourn in transitional fields, and their final settling in the developing CNS. (3) Construct quantitative timetables of the birth dates of different classes of mature neurons in different components of the adult rat CNS. The results of these studies were published in a series of journal articles (see Introduction, Part ID), and were reviewed in chapters contributed to edited books (Altman, 1992; Altman and Bayer, 1975, 2004; Bayer and Altman, 1995a, 1995b, 2004b). We embarked on this ambitious project for two reasons. First, to fill a gaping void in the literature on this important subject. There is currently no comprehensive atlas available that covers the entire time span of prenatal human CNS development from the time when the neural tube and the brain vesicles close (approximately GW3) until birth at the end of the third trimester (approximately GW37). Although there are many published accounts of certain facets of the early development of the human CNS (mostly in volumes of the Carnegie Institution of Washington, Contributions to Embryology), and a few published overviews of human brain development (e.g., Sidman and Rakic,
1982), as well as books on its early phases (e.g., Gasser, 1975; O’Rahilly and Müller, 1994), this five-volume atlas is the first comprehensive source that provides a detailed description of the entire course of this momentous morphogenetic event. There are obvious needs for a detailed description of the prenatal development of the human brain and spinal cord: (i) as an aid to medical practitioners, (ii) as a reference work for molecular, physiological, and behavioral neurobiologists, and (iii) as an empirical foundation for the ethical, legal, and psychological assessments of the putative mental status of the human embryo and fetus. Second, we hoped that by extrapolating from the experimental data obtained in animals, we could go beyond a mere narrative account of developmental landmarks in human CNS development to a dynamic analysis of some of the morphogenetic processes involved. What we were surprised to find is that our detailed examination of the full course of CNS development in normal human embryos and fetuses has come to shed new light on some of the basic mechanisms involved in the production, migration, differentiation, and assembly of CNS neurons, and some aspects of its afferent and efferent wiring and circuitry formation. We begin here with a brief overview of these insights and provide some of the details with summary illustrations and documentation in the succeeding sections.
A. Overview The Beginning of CNS Development: Stockbuilding NEP Cells and the NEP Matrix. An examination of the CNS of an older embryo or fetus may give the impression that the germinal matrix lining the ventricle (the ependymal layer of classical neuroanatomists and the ventricular zone of modern ones) is merely one of its laminar constituents, one that generates neurons and neuroglia for its more mature strata. In fact, for several weeks after closure of the neural tube, the human CNS consists only of a proliferative matrix of NEP cells and is devoid of differentiating neurons and neuroglia. The proliferating pluripotent or fate-restricted stockbuilding progenitor cells that compose the mosaic compartments of the NEP matrix are the sole constituents of the early-embryonic CNS. As development proceeds, the stockbuilding NEP cells give rise, at different rates in different NEP compartments, to differentiating (postmitotic) daughter cells. The latter exit the proliferative NEP matrix and start to form the differentiating elements of the brain parenchyma.
427 The Superventricles and their Variegated Shorelines. We offer evidence that, after closure of the neural tube, the mitotic division of stockbuilding NEP cells is promoted by the hypertrophied telencephalic, diencephalic, mesencephalic, and rhombencephalic superventricles. Because stem cell nuclei of the pseudostratified NEP matrix have to shuttle to the ventricular lumen to undergo mitosis, the areal extent and configuration (protuberances, eminences, invaginations, etc.) of the variegated superventricular shorelines, and their persistence over time, are a limiting factor in determining the population size of the neurons generated at different NEP locations. For instance, the immense growth of the cerebral and cerebellar cortices in the human CNS is dependent upon the immense expansion and long endurance of the telencephalic and rhombencephalic superventricles, respectively. Moreover, the cerebrospinal fluid of the superventricles and the hypertrophied embryonic telencephalic and rhombencephalic choroid plexuses may contain trophic factors that promote NEP cell proliferation.
an important role in the early evolution of the invertebrate and protochordate CNS, the overriding principle of CNS development in lower and higher vertebrates (including humans) is NEP mosaicism, the progressive diversification of progenitor compartments to generate neural systems with distinctive functions.
The Superarachnoid Reticulum as a Parenchymal Expansion Field. As first identified in the present volume, the developing human brain is encased during the first trimester in the superarachnoid reticulum, a transiently inflated and spongy meningeal tissue sandwiched between the pial membrane, adjacent to the brain, and the formative dural membrane, adjacent to the mesenchymal tissue that will form the skull. The initial enlargement of the superarachnoid reticulum antedates the onset of neuronal migration and differentiation, providing expansion space for the settling neurons, their afferent and efferent fibers, and other differentiating components that form the developing brain parenchyma. Accordingly, we propose that during the embryonic and early fetal periods, components of the hypertrophied superarachnoid reticulum serve as regional parenchymal expansion fields. The superarachnoid fluids may contain trophic factors that promote NEP cell differentiation.
Neuronal Migration, Sojourning, and Transitional Fields. Although the fate-specification of neurons begins before they leave their NEP compartments, their ongoing diversification is dependent on subsequent events, beginning with their migration, sojourning, and interactions with other neural elements along their trajectory. Instead of a uniform principle of cell migration, the available evidence suggests great diversity in the patterns and mechanisms used by different translocating neuronal populations and their dependence on different guideposts and signaling agents. Some classes of neurons migrate a short-distance, others follow a long course; some neurons migrate singly or in small groups, others form chains or large streams; some neurons move radially, others take a tangential or a tortuous path; some neurons move directly to their final destination, others sojourn for a shorter or longer period in transitional fields where they are subjected to different influences and where they may establish transient or enduring connections with other neuronal systems.
Metamerism versus Functional Mosaicism as Principles of CNS Development. According to the popular metameric hypothesis, the mammalian neuraxis is composed of a large number of reiterated transverse blocks or segments. However, the evidence we present indicates that the diverse NEP components of the dorsal and ventral mesencephalon, diencephalon, and telencephalon give no hint of a metameric organization at any phase of their development. While the trunk region and the spinal cord are distinguished by peripheral segmentation (the reiterated somites and the dorsal and ventral roots), the central gray matter of the spinal cord has a longitudinal (columnar) rather than a segmental organization. And while the rhombencephalon shows distinctive central neuromerism at a certain stage of its development, the different rhombomeres are not reiterated units but highly diversified NEP mosaics (see below). Although peripheral metamerism probably played
The Rhombomeres as NEP Mosaics. Contrary to the widely held view that the head-related rhombomeres are reiterated segmental units, analogous to the trunk-related peripheral somites and spinal ganglia, we present morphogenetic evidence that rhombomeres 2 to 7, are transient NEP mosaics that are directly linked with different cranial ganglia—the trigeminal, facial, vestibulocochlear, glossopharyngeal, and vagal ganglia—and morphogenetically related to the branchial and epibranchial placodes that, together with neural crest cells and some mesenchymal elements, give rise to such diverse structures as the face, the jaws, the palate, the inner ear, the upper gut, and several visceral organs.
The Secondary Germinal Matrices. Proliferative NEP cells in some regions of the CNS generate not only differentiating neurons but also fate-restricted cells that retain their proliferative potency after they have left the ventricular lumen. These secondary matrices include the SVZ of the neocortex and the basal ganglia, the interstitial subgranular zone (SGZ) of the hippocampal dentate gyrus, and the subpial EGL of the cerebellar cortex and the cochlear nuclei. The secondary germinal matrices persist in many regions for a long time after the primary NEP matrix has disappeared. The neurogenic secondary matrices produce microneurons (like granule cells) with locally arborizing axons that become interdigitated with the earlier-generated larger neurons with long axons. Dispersed, fate-restricted glial progenitor cells in the CNS produce neuroglia that support neuronal growth and repair throughout life.
428 Periphero-Central Induction and Signaling. Functional mosaicism is a product of reciprocal induction and signaling between diversifying NEP matrix compartments and the peripheral or central structures with which they are fated to interact. At the beginning of development, NEP matrix compartmentation has to be coordinated with different peripheral structures: the sensory neurons of the spinal and cranial ganglia, the sense organs they serve, and the different peripheral muscle groups they will innervate. In the trunk region, this periphero-central coordination is accomplished by reciprocal induction and signaling between the spinal NEP and regional neural crest cell populations, the somites, the notochord, and their derivatives (the spinal ganglia, the cutaneous receptors, the developing axial and limb muscles, etc.). In the head region, this coordination is accomplished by reciprocal induction and signaling between the cephalic NEP and the peripheral cranial, branchial, and epibranchial placodes and their derivatives (the olfactory epithelium, the lens, the cranial sensory ganglia, the inner ear, etc.). This coordination occurs during the early first trimester in humans. Current research in experimental animals, which we will briefly review, implicates specific genes, transcription factors, and signaling molecules are involved in this morphogenetic transaction. Centro-Central Induction and Signaling. The higherorder components of the CNS—such as the thalamic relay nuclei, the neocortical sensory and motor projection areas, the feedback loops of the cerebellum and the basal ganglia—have no direct connections with peripheral sense organs and effectors. However, they are intimately associated with one another through large fiber tracts and elaborate regional networks of axon terminals, dendrites and synaptic junctions. The establishment of topographically organized projection systems, and the development of serial or hierarchic interconnections among them, is dependent on centro-central induction and signaling. Current research in animals focuses on the identification of signaling mechanisms involved in the guided pathfinding of axons and the choreographed migration of neurons. In the human CNS, long-range axonal connections are established by the late first trimester but the establishment of the fine circuitry of many brain regions through interdigitation of interneurons and microneurons is a lengthy process that extends beyond the second and third trimesters and continues through the postnatal period of brain development.
B. The NEP Matrix: Stockbuilding NEP Cells, and Differentiating NEP Cells The NEP Matrix. For weeks after uterine implantation, the human embryo lacks a functional CNS with differentiated neurons furnished with dendrites, axons, and intercellular connections that make possible the gathering, conveying, processing, and storing of sensory information and the generation of responses to them by overt movements and
actions. It is only about one month following conception (approximately GW4-4.5) that differentiating neurons start to aggregate in the earliest-maturing regions of the spinal cord (Altman and Bayer, 2001). In the late-developing cerebral cortex, the rudiment of the gray matter, the cortical plate, does not begin to form until approximately GW8-8.5 (Volume 4 of this Atlas). Instead of differentiating neurons, the early embryonic CNS consists of an expanding proliferative matrix of neural stem cells and precursor cells, the neuroepithelium (NEP). The life-career of the NEP matrix begins in the form of a superficial, flat ectodermal sheet, the neural plate, which is recognizable in the human embryo by approximately GW2.5 (O’Rahilly and Müller, 1994). This open NEP matrix is devoid of its own distinctive fluid environment. The ventricular system filled with cerebrospinal fluid (CSF) begins to form at approximately GW3-3.5 when the open neural plate changes into a closed vessel. This takes place as two other ectodermal derivatives, the neural crest and the placodes, differentiate lateral to the folding neural plate. The highly motile neural crest cells give rise to the PNS of the trunk region, including the neurons of the dorsal root ganglia, the sympathetic and parasympathetic ganglia, and enteric nervous system, as well as some non-neuronal elements (Weston, 1970; LeDouarin, 1982). In the head region, neural crest cells are believed to produce some neuronal elements and the facial skeleton, but the peripheral cranial nerve ganglia and components of the head sensors (olfactory, visual, auditory) originate from a distinctive ectodermal matrix, the placodes (Knouff, 1935; Jacobson, 1963; Noden 1993). After separation of the neural crest and the placodes, the neural folds fuse dorsally and that leads, in the trunk region, to the formation of the closed NEP matrix of the neural tube (future spinal cord) and, in the head region, to the formation of the cranial vesicles (future brain). There are initially three cranial vesicles: the prosencephalic NEP (forebrain primordium), the mesencephalic NEP (midbrain primordium), and the rhombencephalic NEP (hindbrain primordium). Then, as a portion of the prosencephalic NEP evaginates and expands laterally, the forebrain rudiment is transformed into a medial diencephalic NEP (future thalamus, subthalamus, and hypothalamus) and a bilateral telencephalic NEP (future cerebral cortex, basal ganglia, and olfactory bulb). Stockbuilding and Differentiating NEP Cells. There are several controversial issues regarding the features and properties of NEP cells that constitute the NEP matrix. One concerns the differences in the cleavage orientation and fate of NEP cells that undergo mitosis near the lumen, another concerns the variable morphology of NEP cells, and still another the typology of NEP cells. It has been noted in the past (e.g., Bayer and Altman, 1991a) that the cleavage plane of NEP cells varies from vertical (perpendicular to the ventricular lining) to horizontal (parallel to the ventricular lining). It has been hypothesized that vertical cleavage results in symmetrical cell division, and hori-
429 zontal cleavage in asymmetric cell division (e.g., Chenn and McConnell, 1995). Symmetric NEP cell division is assumed to produce two neural precursor cells, or what we call stockbuilding cells. Asymmetric cell division is presumed to produce at least one differentiating (postmitotic) neural cell. Presumably the cell located farther from the ventricular lumen withdraws from the mitotic cell cycle, leaves the NEP matrix, and starts the long process of differentiation. From the perspective of the areal extent of the ventricular shoreline, vertically cleaving cells take up twice as much NEP/CSF interface space as the horizontally cleaving cells. Hence, a high rate of symmetric divisions should result in expansion of the ventricular shoreline whereas high rate of asymmetric divisions should result in its shrinkage. Indeed, some evidence has been presented that there is an increase in the asymmetric division of cortical NEP cells in mice as a function of increasing fetal age (Estivill-Torrus et al., 2002). Currently there is considerable interest in the molecular mechanisms that affect the switch from stockbuilding to neurogenic NEP cell division. Notch signaling has been reported to foster expansionary (stockbuilding) symmetric division of NEP cells (Ishibashi et al., 1994; Artavanis-Tsakonas et al., 1999; Alexson et al., 2006). In the absence of repressor type-bHLH (basic helix-loop-helix) genes, which are essential for Notch signaling, NEP cells prematurely differentiate into neurons and neuroglia (Nakamura et al., 2000; Hatakeyama et al., 2004). Transient misexpression in mice of the repressor -type bHLH genes, Hes1 and Hes5, known Notch effectors, results in the expansion of the stockbuilding population of telencephalic NEP cells, but once Hes expression starts to decrease, the NEP cells differentiate into neurons and neuroglia (Ohtsuka et al., 2001). Another consequence of the depletion of repressor type Hes genes is that the premature differentiation of NEP cells prevents the formation of lategenerated astrocytes and ependymal cells (Kageyama et al., 2005). Other molecular factors that appear to promote stockbuilding cortical NEP cell division include C3G, a guanine nucleotide exchange factor (Voss et al., 2006), and ß-Catenin, a protein enriched in adherens junctions at the ventricular lining, since its over-expression produces enlarged cortices in transgenic mice (Chenn and Walsh, 2003). Some stockbuilding genes and factors antagonize genes, while other factors promote cell differentiation. Among the latter are the activator type bHLH genes, Mash1, Math, and neurogenin (Kageyama et al., 2005). Another factor, Aspm, a protein whose mutation is associated with microcephaly (reduced neuron populations) in humans, is down-regulated in NEP cells as they switch from stockbuilding to neurogenic cell division (Fish et al., 2006). It is important to emphasize that the NEP cells which line the ventricles have neither the morphological nor the physiological features of their progeny, the distinctive neurons, neuroglia, ependymal cells, tanycytes, and a few other neural elements of the developing and mature CNS. Dif-
ferentiated neurons reside outside the NEP matrix, have axons, dendrites and synaptic vesicles, and conduct generator and action potentials. In higher vertebrates and humans, the NEP matrix does not contain differentiated neurons. Differentiated neuroglia, likewise, have clear distinguishing anatomical and physiological characteristics. For instance, oligodendrocyte lamellae produce the myelin sheath of axons, astrocyte processes nourish neurons, and the radial glia (like the Bergmann glia of the cerebellar cortex) form compartmental palisades. However, we cannot flatly assert that the NEP matrix does not contain neuroglia because that contradicts the popular current view that some of the cells of the ventricular matrix are “radial glia” (e.g., Malatesta et al., 2000; Hartfuss et al., 2001). However, that designation is not justified and has only led to conceptual confusion. Observations made over a century with the Golgi technique has revealed three types of NEP cells: (1) a round globular cell with its endfoot attached to the ventricular lumen; (2) an oval fibrous cell with its endfoot contacting the ventricle and its thin radial fiber reaching the pial surface; and (3) a detached cell with its leading fiber approaching or reaching the pial surface. (Illustrations of these cell types were provided by Morest, 1970, and Morest and Silver, 2003.) Most (though not all) anatomists have assumed that these NEP cells are neural progenitor cells but differed in viewing them as either different types of precursor cells or different stages of the same cell. The popular notion that the fibrous NEP cells are “radial glia,” a separate cell lineage that guides migrating young cortical neurons toward their targets, was advocated by Rakic (1971). The subsequent demonstration that many of these ventricular cells express the glial marker GFAP (Levitt et al., 1981) reinforced this identification. However, the expression of a marker that in the mature nervous system specifically reacts with glial filaments, does not rule out the possibility that the same marker reacts with transient filamentous elements in non-glial embryonic cells (Bennett, 1987). Indeed, the current demonstration that the majority of mitotic NEP cells with radial fibers are neuron progenitors (Malatesta et al., 2000; Miyata et al., 2001; Tamamaki et al., 2001; Noctor et al., 2002) definitively establishes that the fibrous NEP cells are not specialized glia (like the Bergmann radial glia) but are prototypical NEP cells. In addition to neurons, the fibrous NEP cells may also generate other neural elements, such as astrocytes (Misson et al., 1991). Whether there is any direct relationship between symmetrically and asymmetrically dividing NEP cells, on the one hand, and the globular and fibrous NEP cells, on the other, remains to be determined. In light of our observations in the developing human brain, the fibrous NEP cell may be viewed as a neural progenitor that is in contact with the aqueous medium of the superventricle with its endfoot, and approximates the spongy medium of the pia and superarachnoid reticulum with its radial fiber.
430 C. The Superventricles and the Superarachnoid Reticulum The Superventricles. While the telencephalic, diencephalic, mesencephalic and rhombencephalic ventricles are quite narrow and quasi-tubular at GW3.5 (Figure 15A), they expand considerably during the rest of the first trimester (Figure 15B to 15G). We have named these ballooning embryonic cisterns superventricles (Volume 4: Bayer and Altman, 2006). There is a caudal-to-rostral gradient in the time course of superventricular expansion and shrinkage, with the rhombencephalic superventricle leading and the telencephalic superventricle trailing. There are also differences in the magnitude of superventricular expansion, being less pronounced for the mesencephalic and diencephalic superventricles associated with midline nuclear structures (midbrain, thalamus, hypothalamus) and the rhombencephalic and telencephalic superventricles associated with hemispheric cortical structures (cerebellum and cerebrum). We attribute great significance to the expansion, configurational changes, and shrinkage of the superventricles because the ventricular shorelines provide the substratum for NEP cell mitotic division and because proximity to the ventricular CSF appears essential for that division. In our earlier study of human spinal cord development (Altman and Bayer, 2001; Volume 1: Bayer and Altman, 2002), we documented the relationship between ventral-to-dorsal expansion and shrinkage of the central canal with ventral-to-dorsal thickening and thinning of the NEP matrix. That relationship resulted in early-to-late neurogenetic gradients between ventral horn motor neurons and dorsal horn sensory-relay neurons. We inferred that increased proliferation in a NEP compartment is associated with the expansion of its shoreline in the ventricular lumen. As a NEP compartment produces neurons that leave the matrix, it thins and its ventricular shoreline shrinks. Supporting that inference is the relationship we document in this Atlas between the temporal order in the expansion and shrinkage of different components of the NEP matrix—the lengthening and shortening of their shorelines in the superventricles—and the rise and fall in the number of neurons they generate. The first ventricle that commences to expand to form a cavernous cistern is the rhombencephalic superventricle. As seen in sagittal sections, the rhombencephalic superventricle first forms a dome dorsally as the medullary velum expands (Figure 15A, B). Then, as the medullary flexure forms ventrally it also expands in that direction to form a triangular cavity (Figure 15C, D). The medullary velum then invaginates to produce the expanding rhombencephalic choroid plexus, and the superventricle becomes divided into a metencephalic (cerebello-pontine) pool and a myelencephalic (medullary) pool. Thereafter, the rhombencephalic superventricle begins its gradual shrinkage and eventually assumes the size and form of the familiar fouth ventricle. The expansion of the mesencephalic superventri-
cle (the future aqueduct) and that of the diencephalic superventricle (the future third ventricle) is not as pronounced as that of the rhombencephalic superventricle but is evident when the parenchyma of the mesencephalic tectum and tegmentum, and the diencephalic thalamus and hypothalamus, start to expand. The expansion of the telencephalic superventricles does not commence until approximately GW5.5, when two symmetrical, balloon-like fluid compartments start their lateral outpouching from the midline prosencephalic ventricle. The great expansion of the telencephalic superventricles continues up to approximately GW11. Then, in correlation with expansion of the cerebral cortex and the basal ganglia, the telencephalic superventricles begin to shrink during the second and third trimesters and are eventually transformed into the enduring lateral ventricles. The initial expansion, of the midline prosencephalic superventricle, and then of the bilateral telencephalic superventricles are illustrated in coronal sections in Figure 16A to 16I. How is overall superventricular expansion, in general, and regional differences in the configuration and magnitude of that expansion, in particular, related to neurogenesis? We propose that the area of the variegated ventricular NEP lining, in combination with such important factors as cell cycle speed and the number of mitotic divisions prior to differentiation, determines the size of the neuron population generated at a particular site. This is so because the nuclei of the pseudostratified NEP cells have to undergo “interkinetic nuclear migration” (Sauer, 1936), i.e., shuttle to the ventricular lumen, to undergo mitotic division. That is, the number of NEP cells produced is limited by the surface area (length and width) of the ventricular shoreline because the elongated cells inside the NEP matrix cannot undergo mitosis unless there is room for them to descend to the NEP/CSF interface. The overall extent of the shoreline of a particular superventricle provides the required space for the shuttling NEP cells to continue their cycle of divisions until a specified number of neurons are generated for that brain system; the variegated regional size or configuration of the shoreline—in the form of expanding and shrinking eminences, protuberances, evaginations and invaginations into the ventricle—provide the required space for the production of the right number of neurons for a specific brain region or structure within that brain system. In general, NEPs lining ventricular surfaces that produce large cortical structures composed of similar neuronal populations (e.g., the neocortical, tectal, and cerebellar NEPs) tend to be extensive and smooth, whereas the NEPs lining ventricular surfaces that produce a multitude of distinctive but smaller neuronal populations (e.g., the NEP mosaics that produce the various thalamic and hypothalamic nuclei) tend to be small and corrugated. The correlation between ventricular size and the magnitude of the generated neuronal population is illustrated in a comparison of the area of the telencephalic superventricle (specifically, its cortical pool) between the rat that develops a small neoText continues on page 435
431
A. C7724
GW3.8
B. C9297 GW4
expanding diencephalic and mesencephalic superventricles
expanding rhombencephalic superventricle
C. C1390 GW7
Invaginating rhombencephalic choroid plexus
expanding telencephalic superventricle
D.
C632 GW7.7
Anchoring point of pontine flexure
shrinking rhombencephalic superventricle
Medullary velum
Figure 15. Expansion of the superventricles (light and dark blue) in embryos of estimated ages between GW3.8 and GW7.7 (A-D). Note the temporal difference between the expansion of the rhombencephalic and telencephalic superventricles. Sagittal sections.
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GW3.2 Cephalic preplacode open anterior neuropore
Stockbuilding closed prosencephalic NEP
B. C836
GW4
Figure 16. Summary of ventricular expansion in coronal sections of the forebrain on this and the following two Open prosen- pages. The open prosencephalic NEP in cephalic a GW3.2 embryo (A). Expansion of the NEP medial prosencephalic superventricle (blue) between GW4.0 and GW5.0 (BD), and of the paired lateral telencephalic superventricles between GW5.5 and GW8.3 (E-I). Note the direct relationship between the expanding telencephalic superventricles and the NEP/placodal expanding fetal choroid plexus (green). junction
expanding prosencephalic superventricle
Cephalic preplacode
Olfactory placode Cephalic preplacode
C. M2300
GW4.5 Stockbuilding prosencephalic NEP
Mesenchymal densities associated with growth of olfactory nerve (I)
Primordial mesenchymal brain case (skin, bone, meninges)
expanding prosencephalic superventricle
Olfactory placode
Cephalic preplacode
D. C8314 GW5
Primordial mesenchymal brain case (skin, bone, meninges)
Pial blood islands
Stockbuilding prosencephalic NEP
Mesenchymal densities associated with growth of olfactory nerve (I)
Olfactory placode
expanding prosencephalic superventricle
E.
433 Choroid plexus M1000 stem cells GW5.5 Expanding cell-sparse superarachnoid reticulum Stockbuilding dorsal telencephalic (cortical) NEP
Figure 16 continued. Pia roof of diencephalic superventricle foramen of monro
expanding telencephalic superventricle
Cell-dense future skin, bone, and dura Stockbuilding basal telencephalic/ basal ganglionic NEPs
F.
Pioneer migrating neurons
Choroid plexus stem cells
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Diencephalic
Cell-dense future skin, bone, and dura
Telencephalic
Expanding cell-sparse superarachnoid reticulum (brain is growing into this space)
Limbic cortical
Pia
Neocortical
No cortical neuronal migration
Stockbuilding telencephalic NEPs
expanding telencephalic superventricle
Limbic cortical
Pioneer migrating neurons
Budding choroid plexus (stage I)
roof of expanding diencephalic superventricle
foramen of monro
Basal ganglionic
More basal ganglionic/ basal telencephalic neuronal migration and settling Basal telencephalic Septal
Cell-dense future skin, bone, and dura
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Cell-sparse superarachnoid reticulum shrinks as brain grows
GW7
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Stockbuilding telencephalic NEPs
Cortical neuronal migration begins in lateral limbic cortex
Budding choroid plexus (stage II)
Vascular bed of choroid plexus
foramen of monro
Ventricle Superarachnoid Choroid plexus
expanding telencephalic superventricle
roof of expanding diencephalic superventricle
Migrating and settling basal ganglionic/ basal telencephalic neurons accumulate in the expanding parenchyma
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Figure 16 concluded. Cell-sparse superarachnoid reticulum continues to shrink as brain grows
Limbic cortical
GW7.6
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Primordial plexiform layer in medial limbic and neocortex
Stockbuilding telencephalic NEPs
expanding telencephalic superventricle
Neocortical
(dorsal pool)
Cortical transitional fields first appear in lateral limbic and neocortex Limbic cortical
Expanding choroid plexus invades dorsal telencephalic superventricle
(lateral)
Cortical plate first forms in lateral limbic cortex
shrinking telencephalic superventricle
Basal ganglionic
(ventral pool) Basal telencephalic
Basal ganglionic, basal telencephalic, and septal neurons continue to accumulate in the expanding parenchyma Septal roof of diencephalic superventricle (above foramen of monro)
Ventricle Superarachnoid
I.
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Thin cortical plate in medial limbic and neocortex Thin, cell-sparse arachnoid reticulum borders rapidliy expanding cerebral cortex
Stockbuilding telencephalic NEPs expanding dorsal telencephalic superventricle
Thick cortical plate in lateral limbic and neocortex
Choroid plexus expands in dorsal telencephalic superventricle shrinking ventral telencephalic superventricle
foramen of monro shrinking diencephalic superventricle
Continuity between diencephalic and telencephalic choroid plexus
Insular cortex
Basal ganglionic neurons Basal telencephalic neurons
Preoptic area neurons
Shrinking basal telencephalic NEP Shrinking preoptic area NEP
Temporal cortex
Internal capsule fibers enter lateral limbic cortex
Expanding parenchyma 1 mm
435 cortex and the human that develops a very large neocortex (Figure 17). In addition to the ventricular shoreline providing the space for the mitotic division of NEP cells, there is emerging evidence that the embryonic CSF contains trophic molecules that promote NEP cell division. Since we know that the fate-restricted progenitor cells of the secondary germinal matrices—like those of the subpial external germinal layer of the cerebellum (Altman and Bayer, 1982a) and the interstitial subgranular zone of the hippocampus (Altman and Bayer, 1975)—undergo mitosis some distance from the ventricles, the presence of CSF is obviously not required for the proliferation of late-generated microneuronal progenitors (Altman and Das, 1965b). However, proximity to the embryonic CSF may be a prerequisite for the production of the early, pluripotent NEP cells that generate the large projection neurons. This assumption is supported by reports that the embryonic CSF contains a variety of gene products, proteins, and growth factors (Parada et al., 2006), some of which promote NEP cell proliferation and neurogenesis in experimental animals (Gato et al., 2005; Martin et al., 2006; Mashayekhi and Salehi, 2006). What is the origin of the embryonic CSF? In light of the fact that in the mature brain CSF production is dependent on the choroid plexus (CP), it is important to note that the initial great expansion of both the rhombencephalic and telencephalic superventricles antedates by several weeks the formation of the CP (Figure 15 and Figure 16). Moreover, the great flowering of the fetal CP is limited to two sites, the anterior (cerebellar) pool of the rhombencephalic superventricle and the dorsal (neocortical) pool of the telencephalic superventricle. It is significant that in humans, an immensely enlarged CP fills the ballooning telencephalic superventricle as the neocortical NEP vastly expands to produce a large neocortex; compare that to rats where a small CP is in the more flattened telencephalic ventricle as the rat neocortical NEP minimally expands to produce a small neocortex (Figure 17). This suggests that there may be two phases in CSF production in the human CNS: an early phase that depends on a “budding” CP, and a late phase that depends on a “blooming” CP, one that sustains the prolonged production of cortical and cerebellar NEP cells. It should be noted finally that the fetal CP has a different cellular organization than the mature CP (Kappers, 1958; Tennyson and Pappas, 1964; Shuangshoti and Netsky, 1966; Dohrmann, 1970; Dziegielewska et al., 2001; Johansson et al., 2005). The adult CP is a distinctive frond-like tissue composed of a monolayer of differentiated cuboidal cells that surround a capillary core. The exposed surface of these cuboidal cells is covered by a rich meshwork of microvilli and some cilia, and the cell interior is filled with mitochondria. In contrast, the fetal CP is a smooth, multilayered (pseudostratified) epithelium composed of spindle-shaped cells that have a simple exposed surface and contain few mitochondria. Unlike the mature CP cells, these fetal CP cells are full of glycogen. Hence,
it may be that one of the functions of the embryonic CP is the glycolytic (anaerobic) support of NEP cell proliferation and neurogenesis. The Superarachnoid Reticulum. The mature brain is surrounded by a tripartite membranous envelope, the meninges, composed of the fine pia mater abutting the brain parenchyma, the tough dura in contact with the bony skull, and the spongy arachnoid sandwiched between the two. The pia is composed of a network of reticular and elastic fibers that adhere to the underlying neural tissue. The dura is formed of connective tissue that serves both as a protective envelope of the brain and as a periosteum of the skull. The interlacing cobweb-like processes of the arachnoid form the spongy subarachnoid space filled with CSF, containing granulations, villi, septa and other regional modifications in relation to the local distribution of blood vessels, perivascular spaces, and venous sinuses. Little information is currently available about the features and properties of the embryonic meninges (Angelov and Vasilev, 1989; Kamiryo et al., 1990; Sturrock, 1990). A study of the development of the human optic nerve emphasized the presence of glycogen-rich cells in the dura and arachnoid (Sturrock, 1987). Observations we present in this Volume indicate that of the three components of the meninges, the pia emerges early during human brain development but the dura much later. Before differentiating neurons start to leave the NEP matrix, a thin tissue layer separates the brain primordium from the surrounding celldense (darkly staining) mesenchymal tissue that will later form the skin and bone of the skull. Associated with the development of this formative pia, a cell-sparse (lightly staining) field emerges between it and the cell-dense mesenchyme. This cell-sparse field expands enormously as the brain parenchyma grows through the first trimester, and has variably sized divisions in relation to the different developmental dynamics of components of the telencephalon, diencephalon, mesencephalon and rhombencephalon. We call this embryonic meningeal field the superarachnoid reticulum (Figure 18A to 18D). (We must note here that we have failed to recognize this unique feature of the developing brain in the GW7.5 specimen illustrated in Plates 186 to 206 in Volume 4 of the Atlas [Bayer and Altman, 2006], where we simply referred to the region as the “meninges.”) As the dura gradually becomes recognizable, the superarachnoid reticulum is seen to become enclosed by an internal and external network of blood vessels associated with the pia and the dura, respectively. By about GW9, the superarachnoid greatly diminishes in size (Figure 18E) and the meninges gradually assume their mature form. Because the expansion of the superarachnoid reticulum antedates the growth of the brain parenchyma (Figure 18A to 18C), and the brain parenchyma subsequently expands into the space formed by it (Figure 18D, E), we postulate that the superarachnoid reticulum constitutes a parenchymal expansion field, a site that is being readied for (and possibly promoting) the entry of differentiText continues on page 441
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A. Rat, embryonic day 18 lateral ventricle
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Figure 17. Comparison of the relative size of the cortical division of the telencephalic superventricle (dark blue) in the rat, which develops a small neocortex and humans, which develops a large neocortex, in sagittal (A and B, this page) and coronal (C and D, facing page) sections. Note the correlated difference in the size of the choroid plexus (green) in the two species.
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C. Rat, embryonic day 18
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438 mesencephalic superventricle with surrounding mesencephalic NEPs
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Medullary velum
prosencephalic superventricle rhombencephalic superventricle
closed anterior neuropore
Superarachnoid reticulum
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Surrounding rhombencephalic NEPs
halic diencep tricle en superv
Surrounding prosencephalic NEPs
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Medullary velum
c li ha le ep ic nc tr be ven om er rhsup
Incipient invaginating rhombencephalic choroid plexus
Superarachnoid reticulum (continues to expand around the entire brain in advance of parenchymal growth)
Ventricle Superarachnoid
1 mm
Choroid plexus
Figure 18. Expansion of the superarachnoid reticulum (yellow) between the pia and the formative dura between GW4.0 and GW8.0 (A-D, this and the facing page) followed by its shrinkage by GW9 (E). Sagittal sections.
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STOCKBUILDING NEPs Figure 19. Schematic drawing of the embryonic human CNS with the expanding superventricles (blue) that provide the extended shoreline for the mitotic division of stockbuilding NEP cells, and the expanding superarachnoid reticulum (yellow with blue) that serves as the parenchymal expansion field for the migrating and settling neurons.
© 2008 by Taylor & Francis Group, LLC
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rd Dorsal spinal co al central can cord Ventral spinal
441 ating neurons and their processes into the developing brain tissue. We speculate that the two fluid-filled spaces, the expanding superventricles and the superarachnoid reticulum—interconnected by the rhombencephalic and telencephalic tela choroidea (Figure 19)—play a complementary role in CNS development, trophic factors in the superventricular CSF promoting expansion of the stockbuilding NEP cell population, and trophic factors in the superarachnoid CSF promoting neuronal differentiation and migration.
D. Metamerism or Mosaicism as Principles of CNS Development From Metamerism to Functional Compartmentation. It is a popular current hypothesis that the neuraxis that extends from the caudal spinal cord to the rostral forebrain develops from a series of reiterated segments or metameric units. This idea goes back to pre-Darwinian evolutionary speculations of early 19th-century thinkers, such as Oken and Goethe, who argued that the vertebrate skull is composed of a number of transformed vertebrae (de Beer, 1937; Starck, 1963). That is, the head is but a modified rostral portion of the trunk. An extension of this idea was that, much as the axial spinal cord is divided into so many transverse segments by the entering and exiting dorsal and ventral spinal nerves, so also the brain is built from a series of transverse units, the neuromeres. This view was supported by the identification of a set of 7 or 8 protuberances, the rhombomeres, in the developing vertebrate hindbrain in association with some of the cranial nerves (Orr, 1887; Vaage, 1969). This view has currently found some support from studies that use genetic markers and mutants to analyze the features of the different rhombomeres (Lumsden and Krumlauf, 1994; Gavalas et al., 1998, 2003) and metamerism has been extended to the midbrain and forebrain by postulating the existence of the so-called prosomeres (Rubinstein and Puelles, 1994). However, an analysis of what is meant by “segmentation” or “metamerism “ when applied to different components of the body and the CNS reveals conceptual inconsistencies. Segmentation in the trunk (somitomerism) is principally a peripheral phenomenon. It is manifested during early development by the presence of reiterated morphogenic blocks, the somites, and as the PNS develops later, by the formation of the segmental dorsal root ganglia and dorsal and ventral spinal nerves in relation to reiterated dermatomal and myotomal compartments. This peripheral segmentation, which is an ancient chordate legacy (Romer, 1970) persists throughout life with profound topological transformations in all vertebrates, including humans. Significantly, however, there is no central segmentation (transverse partitioning) in the vertebrate spinal cord. On the contrary, the vertebrate spinal cord (unlike the neuraxis of many invertebrates) is a longitudinally organized morphogenetic and functional system. The spinal NEP is a con-
tinuous proliferative matrix through its entire length. And as differentiation begins and progresses, the motor neurons of the ventral horn form longitudinal columns, and the sensory neurons of the dorsal horn extend from lower lumbar levels to upper cervical levels without any transverse partitioning (e.g., Altman and Bayer, 2001). In contrast to the enduring peripheral metamerism in the spinal cord, the metamerism in the rhombencephalon, the reiterated NEP bulges known as rhombomeres, is an instance of transient central segmentation. Although there are indications for some peripheral metamerism here, too, in the form of vestigial gill arches (branchiomerism), these reiterated structures of ancestral protochordates have become transformed into structurally and functionally diversified cranial organs in vertebrates (Shimeld and Holland, 2000). In contrast to the reiterated trunk somites, the cranial primordia and placodes (see below) give rise to such diverse specialized structures as the jaws, various oro-facial organs, the inner ear, the pharynx, and certain viscera that are absent in the trunk region. Moreover, the cranial ganglia associated with these various organ systems—trigeminal, facial, vestibular, spiral, glossopharyngeal, and vagal ganglia—are not reiterated structures like the spinal ganglia but functionally diversified sensory systems. There is no empirical evidence to support the idea of a metameric organization either in the skull or the rostral CNS (mesencephalon, diencephalon, telencephalon). Even in the most primitive extant vertebrate, the lamprey, the mesoderm is segmented along the trunk but not in the head region (Kuratani et al., 1999). Nor is there evidence that the different brain vesicles are reiterated metameric units. For instance, the two transverse “segments” of the tectum in the dorsal mesencephalon (the inferior and superior colliculi) are structurally and functionally quite dissimilar structures, one being the target of auditory fibers from the medulla, the other of optic fibers from the retina. The multifarious structures in the tegmentum of the ventral mesencephalon, the red nucleus, the oculomotor nuclear complex, the periaqueductal gray, the substantia nigra, the ventral tegmental area, the interpeduncular nucleus, etc. provide not even a hint of reiterated transverse organization. The same applies to the diencephalon and the telencephalon. Compartmentation in components of diencephalon (optic vesicle, thalamus, subthalamus, preoptic area, hypothalamus, etc.) and compartmentation in the telencephalon (olfactory bulb, neocortex, hippocampus, striatum, amygdala, etc.) cannot be fitted, by any stretch of the imagination, into a reductionistic metameric framework. We do not deny metamerism is a facet in the early development of body and brain in vertebrates, man included, but we question its significance as an overriding morphogenetic principle of CNS development. Specifically, we look upon metamerism as a protochordate and protovertebrate legacy, a phylogenetic burden that was gradually overcome as the segmented, limbless, and headless worm-like ances-
442 tral lines acquired a far more complex body structure with a functionally integrated CNS in the course of vertebrate evolution. The story may have begun with an ancestral protochordate, not unlike the extant Amphioxus. Amphioxus spends most of its time buried in gravel or sand and uses its oral cilia and gills to filter nutrients suspended in the water (Buchsbaum, 1948). The mesoderm of Amphioxus is segmentally organized, with bilaterally arranged muscle blocks along its elongated body which resembles that of a fish. The wave of alternate contractions of these muscle blocks produces the undulatory swimming motion that allows Amphioxus to flee when disturbed. The spinal cord of Amphioxus is situated above the notochord (the phylogenetic and ontogenetic precursor of the vertebral column of vertebrates), and it shares many features with the spinal cord of vertebrates, such as the dorsal position of the sensory nerves and the ventral position of the motor nerves (Bone, 1960). However, the bipolar sensory neurons of Amphioxus are located in the spinal cord centrally rather than peripherally in the spinal ganglia (as in vertebrates), and its motor neurons are located near the spinal canal rather than in the ventral horn. Moreover, Amphioxus lacks a true brain. As a sedentary filter feeder, Amphioxus survives without having a head furnished with specialized sense organs and a specialized muscular oral apparatus. Instead of eyes, it has a few pigmented photosensitive cells near the anterior tip of the spinal cord, and its “cerebral vesicle,” marked by Otx gene expression (Shimeld and Holland, 2000), is composed of little more than a few dopaminergic and serotoninergic cells (Lacalli, 2001; Ekhart et al., 2003; Moret et al., 2004). It has been argued that Amphioxus is a degenerate chordate. Another possibility is that a closely related filter-feeder species was the ancestor of more advanced chordates who, by acquiring cranial sense organs and a brain, became enabled to cruise freely in the open waters and turn into successful scavengers, grazers, or predators. The recent discovery of fossil chordates from 520 million-year-old Lower Cambrian beds, named Haikouella and Yunnanozoon, may bridge the gap between these two lines of chordates (Holland and Chen, 2001; Mallatt and Chen, 2003). Haikouella had a body similar to Amphioxus and a head furnished with some sense organs and a small bilobed brain. If this scenario is correct, the quasi-segmental spinal cord is a protochordate legacy, with the proviso that it became further elaborated as the notochord became transformed into an articulated cartilaginous or bony vertebral column and a rib cage, and as the neural crest-derived dorsal root ganglia became exteriorized in more advanced fish. The transformation of sedentary chordates into mobile fish required the development of a head with specialized information-gathering sense organs—the olfactory, visual, auditory, vestibular, lateral line, and gustatory systems— and such specialized motor mechanisms as the muscular mouth of jawless fish and the skeletomuscular jaw of more advanced fish. The trunk also became modified as the
segmentally mediated undulatory swimming was supplemented by fin action for better postural control and maneuverability. As the extremities evolved in tetrapods, body and head organization became more complex, requiring modification of existing neural systems and the formation of new ones. Contrary to the idea that the skull and face are modified vertebral segments, and the brain a modified spinal cord, it appears more likely that most cranial organs and the brain mechanisms serving them evolved de novo. This is supported by the accumulating evidence that different morphogenetic mechanisms are involved in the regulation of spinal cord development and brain development. The spinal NEP surrounding the slit-shaped spinal ventricle is initially uniform in its appearance both in rat (Altman and Bayer, 1984) and humans (Altman and Bayer, 2001; Volume 1 of this Atlas). But then the spinal ventricle changes its shape and a ventrodorsal compartmentation becomes apparent, with the ventral NEP starting to generate the motor neurons of the expanding ventral horn and, later, the dorsal NEP starting to generate the sensory neurons of the dorsal horn. The ventrodorsal compartmentation in the spinal cord is under the inductive influence of the neural crest and two peripheral structures, the somites and the notochord. The sheet of crest cells that spins off the dorsal neural fold and migrates toward the discrete somites, give rise to the neurons of the segmented dorsal root ganglia, and these exert a “dorsalizing” influence upon the dorsal spinal NEP. The unsegmented notochord, in contrast, exerts a “ventralizing” influence on the ventral spinal NEP to generate the motor neurons of the ventral horn. The early differentiation of motor neurons depends on Shh (sonic hedgehog) signaling that is transmitted from the notochord and the floor plate to the ventral NEP (Briscoe, 2000), and retinoids and FGFs (fibroblast growth factors) have been implicated in the rostrocaudal axial specification of spinal motor neurons (Liu et al., 2001). The morphogenesis of the brain obeys different principles than the spinal cord. The somites are absent and the notochord is often indistinct. There is no evidence for comparable dorsalizing and ventralizing influences upon the development of the rhombencephalic, mesencephalic, and telencephalic NEPs. Here the principal inductive influence emanates from two altogether different cranial structures that are absent in the trunk region, the gill arches and the cranial and branchial placodes. The Rhombomeres as NEP Mosaics. As illustrated in this volume of the Atlas, the rhombencephalic NEP has several components. (i) The upper rhombic lip region and (ii) the lower rhombic lip region dorsally form the bridgeheads of the membranous medullary velum that covers the rhombencephalic superventricle. (iii) The less clearly defined ventromedial NEPs are the source of several pontine and medullary motor nuclei. (iv) The ventrolateral NEPs form distinct rhombomeres. The region of the upper rhombic lip NEP is the direct or indirect source of neurons of the cerebellum. The region of the lower rhombic lip
443 NEP is the source of the neurons of the precerebellar nuclei (inferior olive, basal pontine gray, etc.) and the cochlear nuclei. The rhombomeres, a set of conspicuous semicircular NEP evaginations, are the most often cited example of brain metamerism. The exact number of rhombomeres has been controversial (the old literature is reviewed by Vaage, 1969); in the currently popular numerical designation, there are seven rhombomeres (R1-R7), where R1 refers to the cerebellar NEP. This is unfortunate because the cerebellar NEP has little in common either structurally or functionally with rhombomeres R2-R7, which do share some common properties. As we shall describe later, the expanding and long-enduring cerebellar NEP is largely connected with second- and higher-order central afferent systems (some first-order vestibular input excepted), in contrast to the transient rhombomeres that are intimately associated with the first-order peripheral afferents of cranial sensory ganglia. According to Bartelmez and Evans’ (1925) observations in human embryos, R1 and R2 originate from prorhombomere A, R3 and R4 from prorhombomere B, and R5-R7 from prorhombomere C. A similar pattern has been described in mouse embryos (Osumi-Yamashita et al., 1996). According to the latter study, crest cells from prorhombomere A (R2?) migrate into the first branchial arch and produce the trigeminal (V) ganglion; crest cells from prorhombere B (R3 and R4) migrate into second arch and produce the facial and vestibulocochlear (VII-VIII) ganglia; crest cells from the anterior portion of prorhombomere C (R5 and R6) migrate into the third arch and produce the glossopharyngeal (IX) ganglia; and crest cells from the posterior portion of prorhombere C supply cells to the fourth arch and the vagal (X) ganglia. Our observations, which start at a later developmental stage (about 17 to 18 pairs of somites) than those described by Bartelmez and Evans (2 to 16 pairs of somites), indicate a close association between the rhombomeres and the branchial placodes, and the following developmental pattern. In the youngest embryo (estimated age GW3.2), in which the rhombencephalic superventricle is just beginning to expand, three evaginating bulges are evident caudal to the cerebellar NEP (Figure 20A). The first is contiguous with the condensing, small trigeminal ganglion inside the maxillary process. We designate this germinal mosaic as the trigeminal NEP (R2), the target of future cranial nerve V fibers. The affiliation of the second rhombomere (presumably R3) is unclear; we hypothesize that it is the facial (nerve VII) NEP. According to a recent study, R2-derived neuronal progeny contribute to the lower jaw somatosensory representation, and R3 progeny to whisker representation in the barrel fields of mice (Oury et al., 2006). It is possible that the facial NEP is mostly a source of efferents that start to sprout after the facial motor neurons leave R3. (The roundabout migration of facial motor neurons, whose trailing axons form the loop [genu] of the facial nerve, is well known [Altman and Bayer, 1982b]). The third evagi-
nating early rhombomere is aligned with the condensing vestibulocochlear ganglion (nerve VIII) and the otic vesicle. We presume this rhombomere will become subdivided into R4-R5, as seen in a slightly older embryo (estimated age GW4.0) with a greatly expanded rhombencephalic superventricle (Figure 20B). As we documented over two decades ago in the rat (Altman and Bayer, 1982b), the otic vesicle is the source not only of the non-neural elements of the inner ear but also of a large contingent of delaminating neurons, either the neurons of the spiral ganglion and/or some components of the vestibular ganglion. R6 and R7 are not evident in the GW3.2 embryo (Figure 20A) but are beginning to evaginate in the GW4.0 embryo (Figure 20B) and are pronounced in a somewhat older embryo (Figure 20C). In the latter, R6 is aligned with and is in direct contact with afferents of superior glossopharyngeal ganglion, the source of the sensory fibers of cranial nerve IX, and R7 with superior vagal ganglion, the sensory component of nerve X. Accordingly, we designate R6 as the glossopharyngeal NEP, and R7 as the vagal NEP. If this interpretation is correct, the oro-facial peripheral and central systems innervated by the future cranial nerves V and VII, and the vestibulocochlear systems innervated by the future cranial nerve VIII are developing before the pharyngeal-visceral systems innervated by the future cranial nerves IX and X. By GW5, the rhombomeres begin to shrink (Figure 21A); by GW7, they are no longer recognizable in the developing pons and medulla (Figure 21B). Although we stress here the sensory affiliations of the rhombomeres, there is ample evidence from animal studies that the rhombomeres are also a source of motor neurons (e.g., Lumsden and Keynes, 1989). According to a recent study in larval and adult frogs (Straka et al., 2006), trigeminal efferents are derived from R2-R3; facial and vestibular efferents from R4-R5; glossopharyngeal efferents from R6; and vagal efferents from R7 and the rostral medulla and the spinal cord. However, in the human specimens we have examined we find only cranial afferents entering the rhombomeres and no evidence of exiting motor fibers. This may be because either axonal outgrowth occurs after the transient NEP rhombomeres are no longer recognizable as such or axonal sprouting commences, as is well known in the case of facial nerve, after the migrating motor neurons have left the rhombomere NEPs. Timetables of the Development of Placodes, Cranial Ganglia, and Rhombomeres. Whereas in the trunk region, crest cells generate the peripheral neurons of the spinal (dorsal root) ganglia (Weston, 1970; LeDouarin, 1982), the principal source of neurons of the cranial ganglia in the head region are the placodes (Knouff, 1935) or, more accurately, the cephalic and branchial preplacodes that later become divided into specialized placodes (Jacobson, 1963; Noden 1993). The cephalic and branchial preplacodes, formed by pluripotent stem cells, are thickened epithelia that extend from the vicinity of the forebrain NEP to the Text continues on page 446
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A.
B.
C.
A few rhombomeres are definite in the rhombencephalic NEP.
Each rhombomere is well defined as a small convex NEP evagination.
The rhombomeres reach their peak definition from each other.
M714 GW3.2
C836 GW4
M2321 GW4.3
Mesencephalic NEP
Mesencephalic NEP
Cerebellar NEP?
Trigeminal ganglion near R2 NEP
R2 Trigeminal ganglion (V)
R2
R2 R3
Trigeminal boundary cap
R3 Vestibulocochlear ganglion (VIII)
R4/5
Epithelium R6?
R3
R4
R4
R5
Lumen
Otic vesicle
Vestibulocochlear ganglion near R4 NEP
R5
R6
R7? Vagal ganglion (X) R7
Glossopharyngeal ganglion (IX, near R6 NEP)
R6
Otic vesicle near R5 NEP
Spinal NEP R7 Vagal ganglion (X, near R7 NEP)
Somites
Spinal NEP
Figure 20. Formation of the rhombencephalic neuroepithelial bulges (rhombomeres) between GW3.2 and GW4.3 (A-C) in relation to the sensory ganglia of the cranial nerves. Coronal sections. (Serial sagittal sections from a GW5 embryo are shown in Figure 27).
Spinal NEP
Somites
A. C8966, GW5
B. C1390, GW7
isthmal canal
Nerve IV (trochlear)
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
Cerebellar NEP
mesencephalic superventricle
US HM IST
ISTHMUS
Mesencephalic (isthmal) NEP
Mesencephalic (isthmal) NEP
Upper rhombic lip
Pontine NEP
PONS
Cerebellar NEP
Upper rhombic lip Medullary velum
rhombencephalic superventricle
Medullary velum
R2 R3
rhombencephalic superventricle
Facial nerve genu (VII)
Pontomedullary trench (site of the earlier R3?)
Medullary NEP
R4
Rhombencephalic choroid plexus
R5 Rhombomeres are in the medullary and pontine NEP.
Lower rhombic lip
R6
RHOMBENCEPHALON
R7
Rhombomeres have disappeared.
MEDULLA
Lower rhombic lip
Solitary tract
Figure 21. Rhombomeres present in a GW5 embryo (A) disappear by GW7 (B). Sagittal sections.
445
446 border of the trunk region. The different hypothetical origins of neurons of the spinal and cranial nerve ganglia, prior to fusion of the neural tube and the brain vesicles, is illustrated in Figure 22. As seen in a coronal section of a GW3.2 embryo, the cephalic preplacode is continuous with the prosencephalic NEP prior to the fusion of the anterior neuropore (Figure 23A). It abuts the ventral and ventrolateral prosencephalon but is notably absent over the dorsal prosencephalon and farther caudally (Figure 23A, B). The cephalic preplacode is continuous, by way of the oral epithelium, with the branchial preplacode that covers the brachial arches I-IV some distance from the rhombencephalon (Figure 23B). Experiments in animals have shown that, during early embryonic development, the cells of the pluripotent preplacodes are competent to form different special placodes (Jacobson, 1963; Groves and BronnerFraser, 2000). This pluripotency is lost when the preplacodes become partitioned into special placodes that acquire diverse structural and functional properties. The cephalic preplacode divides into the profoundly different olfactory, optic, and pituitary placodes; the branchial preplacode divides to form the diverse domains of the trigeminal, facial, vestibulocochlear, glossopharyngeal, and vagal ganglia. The human embryos we have analyzed in this volume provide chronological information about the developmental course of the peripheral cephalic and branchial placodes, the cranial nerve ganglia they generate, and the emergence and dissolution of the rhombomere NEPs with which they are associated. Thickening of the olfactory placode anteromedially is evident in the GW3.8 and GW4.0 embryos (Figure 24A, B). The formation of the nasal olfactory epithelium and the outgrowth of olfactory nerve fibers is in progress in the GW5.0 and GW5.5 embryos (Figure 24C, D). The vesiculation of the olfactory placode (formation of the nasal cavity) is evident in the GW5.5 embryo (Figure 24D), which also shows the first hint of the evagination of the olfactory NEP. The evagination of the olfactory NEP becomes more and more pronounced between GW6.5 and GW7.5 (Figure 24E to 24I). The presumptive optic lens placode, which surrounds the bulging optic vesicle NEP in the GW3.2 and GW4.0 embryos (Figure 25A, B) thickens in the GW4.5 embryo (Figure 25C) as the invaginating optic vesicle NEP becomes partitioned into a thin pigment epithelium and a thicker retinal NEP. Contrary to the classical view that the evaginating optic vesicle NEP induces placodal lens formation (Spemann, 1938), it has recently been argued that an earlier interaction between the anterior neural plate NEP and a portion of the preplacode establishes a lens-forming bias in the latter (Grainger et al., 1997). The lens placode assumes a spherical configuration in the GW5.0 embryo (Figure 25D) and the onset of the cytological differentiation of the crystalline lens is evident in the GW6 embryo (Figure 25E). The exodus of ganglion cells from the retinal NEP and the sprouting of optic nerve fibers is in progress in the GW7 embryo (Figure
25F). Finally, the formation of the pituitary gland begins in GW3.8-GW5.0 embryos with the folding of the posterior tip of the cephalic preplacode (Figure 26A to 26C). The fusion of this placode between GW5.5-GW6.5 produces Rathke’s pouch, the primordium of the anterior pituitary gland or adenohypophysis (Figure 26D, E). Contiguity between Rathke’s pouch and the posterior pituitary GEP, the neurohypophysis derived from the hypothalamic NEP, is evident in the GW6.0-GW7.0 embryos (Figure 26E to 26H). As noted earlier, the caudal branchial preplacode has two components: a thinner epithelium covering the roof of the oral cavity, which is continuous with the cephalic preplacode, and a thicker portion covering the oral cavity floor (Figure 23B). The latter has several components: the discrete placodes that surround the maxillary process, the mandibular and the hyoid arches (I, II), and visceral arches III and IV (Figure 23B and Figure 27). As it is currently understood, mesenchymal elements of the maxillary process and the mandibular arch are the source of various orofacial structures, such as the jaws, and the visceral arches generate components of the tongue, the pharynx, and the upper gut. The placodes surrounding these diverse structures, together with neural crest cells, are the precursors of sensory cells and of neurons in the cranial ganglia. The latter are the trigeminal (V), facial (VII), vestibulocochlear (VIII), glossopharyngeal (IX), and vagal (X) ganglia. The afferents of these ganglia link various orofacial, inner ear, and gut organs derived from the branchial arches with different divisions of the rhombencephalic NEP. The neurons of the trigeminal and facial ganglia link the orofacial region with rhombomeres R2-R3. As early as GW3.2, a small, spherical trigeminal ganglion is visible near R2 (Figure 20A), and by GW5.0 there is direct continuity between the large trigeminal ganglion and R2 (Figure 27A, B). By that age, three cell-dense arms of ganglion V are identifiable (Figure 28A), and by GW5.5 the ophthalmic, maxillary, and mandibular branches of the trigeminal nerve approximate the eye region and penetrate the maxillary process and the mandibular arch, respectively (Figure 28B). With respect to the central projections of the trigeminal nerve, by GW5.5 the penetrating fibers start to form a bulge at the knee of the pons (Figure 29A, B), and trigeminal fibers clearly intermingle with other fibers of the pontine white matter by GW6.5 (Figure 30A). As early as GW4.0, the vestibulocochlear ganglion is aligned with R4, and the otic vesicle with R5 (Figure 20B). The two are also aligned peripherally with the hyoid arch (Figure 27) but their association is problematic. The afferents of the vestibulocochlear ganglion reach R4 by GW5.0 (Figure 27B), and they penetrate the white matter of R4 and R5 between GW5.5 (Figure 29A, B) and GW6.5 (Figure 30A). The formation of the glossopharyngeal and vagal ganglia, and of R6 and R7 with which they are aligned, is not evident until about GW4.0-GW4.3 (Figure 20B, C). The two are aligned peripherally with the visceral arches III and
447 IV (Figure 27A, B, Figure 29B) but their exact relationship remains to be elucidated. Glossopharyngeal afferents approximate R6, and vagal fibers approximate R7 by GW5.0 (Figure 27B, C), and they penetrate the white matter of R6 and R7, respectively, by GW5.5 and GW6.5 (Figure 25B, Figure 30A, B).
E. Exogenous and Endogenous Mechanisms of NEP Cell Diversification The Role of Periphero-Central Signaling in Placodal and NEP Cell Diversification. An important first step in mosaicism of the NEP matrix is synchronizing its diversification with both somatic and neural development in the body periphery, including the placodes and the peripheral nervous system (PNS). There is emerging experimental evidence that periphero-central coordination is aided by induction and signaling molecules (Baker and Bronner-Fraser, 2001; Streit, 2004). For instance, the rostral cephalic preplacode expresses Six, Eya, and Dach protein markers (Ikeda et al., 2002; Brugmann et al., 2004; Schlosser and Ahrens, 2004; Litsiou et al., 2005) and it has been found that in the presence of both cranial mesoderm and rostral neural plate NEP, excessive Six1 expression expands the preplacode at the expense of the epidermis, whereas Six1 depletion results in a reduction of the preplacodal domain (Brugmann et al., 2004; Ahrens and Schlosser, 2005). The next step in the diversification of the rostral cephalic preplacode is the formation of the olfactory and optic placodes, each with profoundly different structural and functional fates. Whereas the olfactory placode gives rise to the specialized bipolar sensory neurons of the olfactory epithelium, which send fibers to the evaginating olfactory bulb NEP, the optic placode has no neurogenic potential but gives rise to the crystalline lens of the eye. Mutant mice lacking functional Pax6 proteins fail to develop eyes and nasal cavities (Stoykova et al., 1996), and Pax6 and D1x5 are initially expressed in both future olfactory cells and lens-forming cells of the eye (Bhattacharyya et al., 2004). However, as the presumptive lens cells acquire a columnar morphology, D1x expression is reduced in the optic placode whereas Pax6 is lost in the olfactory placode (Bhattacharyya et al., 2004). The authors concluded that loss of D1x is required for the proliferative cells to adopt a lens fate and that the balance between Pax6 and D1x expression regulates cell sorting in the segregating placodes. With reference to periphero-central signaling, it has been reported that extraocular signals affect optic vesicle NEP development (Kagiyama et al., 2005), and that retinoic acid (Matt et al., 2005) and Vax2 signaling are involved in the fate-modification of retinal NEP cells and pigment epithelium cells (Kim and Lemke, 2006). It has also been reported that Mash1 promotes the development of retinal bipolar cells, and Math3 and NeuroD that of amacrine cells (Morrow et al., 1999; Inoue et al., 2002). There is little information about the molecular mechanisms involved in the specification of the third component of
the cephalic preplacode, the pituitary placode, except for the report that targeted disruption of the homeobox genes Nkx2.1, Ttf1, and Titf1 results in the disruption of pituitary gland development (Takuma et al., 1998). A different set of genetic factors and periphero-central signaling molecules appear to be involved in the development of the hindbrain region associated with the branchial placodes. The different rhombomeres express a distinctive combination of Hox genes (Krumlauf, 1993; Wilkinson, 1993; Gavalas et al., 2003; McNulty et al., 2005). Hoxa2 is involved in R2 and R3 specification (Gavalas et al., 1998; Gaufo et al., 2004), and Hoxa1 and Hoxb1 play a role in R4 and R5 specification and the growth of the cranial nerves associated with them (Mark et al., 1993; Arenkiel et al., 2004). Differences have also been noted in the expression of transcription factors Krox20 and Kreisler in the different rhombomeres (Sham et al., 1993; McKay et al., 1994; Schneider-Maunoury et al., 1997; Chomette et al., 2006), and retinoic acid also appears to be involved in rhombomere specification (Niederreither et al., 2000; Dupé and Lumsden, 2001). Members of the Fgf family of signaling proteins, mesoderm-derived Fgf3 and Fgf8, and Ngn2 (Fode et al., 1998; Begbie et al., 2002; Holzschuh et al., 2005; Nikaido et al., 2006; Sun et al., 2007; Nechiporuk et al., 2007) appear to play a role in the early determination and diversification of the epibranchial placodes and their derivatives, the glossopharyngeal and vagal ganglia, and the homeobox genes Phox2a and Phox2b in its later stages (Morin et al., 1997). Among the signaling molecules implicated in the specification of the otic placode and the formation of the inner ear are certain members of the Fgf family (Vendrell et al., 2000; Adamska et al., 2001; Ladher et al., 2005; Nechiporuk et al., 2005; Martin and Groves, 2006) and Ngn1 (Ma et al., 2000). It is noteworthy that gene expression is different in the rhombomeres, where sensory and motor neuron precursors are not obviously segregated, than in the spinal cord where the ventral NEP cells generate motor neurons and the dorsal NEP cells generate sensory interneurons. Mash1 and Math3 are necessary for the development of facial and trigeminal motor neurons (Ohsawa et al., 2005). The genes Frizzled3a and Celsr2 are necessary for cell polarization and the guidance of the roundabout migration of facial motor neurons in the brainstem (Wada et al., 2006), and their migration is also dependent on Phox2b signaling (Coppola et al., 2005). The genes implicated in dorsoventral patterning in the spinal cord are the class II Ssh-promoting Nkx2.2, Nkx2.9, Nkx6.1, and Olig2 genes, and the class I Ssh-repressing Dbx1 and Dbx2 genes (Briscoe et al., 1999; Kessaris et al., 2001; Marquardt and Pfaff, 2001). In light of the profound structural and functional heterogeneity of the cephalic and branchial placodes, we propose that unlike the segmented somites of the trunk, the placodes of vertebrates are not reiterated metameric units but an altogether different kind of progressively diversiText continues on page 451
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SPINAL CORD 1.
Neural crest
Neural groove
3.
Epidermis
Neural plate
2.
BRAIN
Neural fold
Fusing neural tube
4.
1.
Preplacode
2.
3.
4.
Cephalic placodes protoventricle
Spinal ganglion
central canal Neuroepithelium (NEP)
Branchial placodes
Cranial ganglion Dispersing neural crest
Figure 22. Hypothetical differences in the organization of the neural plate of the spinal cord (1-4, left) and forebrain (1-4, right). Neurons of the dorsal root ganglia derive from delaminating neural crest cells, whereas neurons of the cranial nerve ganglia derive from preplacodal stem cells. Cephalic placodes are close to the neuroepithelium, while branchial placodes (on the arches) are farther from the neuroepithelium.
A. GW3.2 Coronal, M714 (Section 18)
B. GW3.8 Sagittal, C7724 (Slide2, Section 30)
Prosencephalic NEP (dorsal)
M
e M
ic r ece s
s
pretecta
l/te
ct
mesencephalic protoventricle
al
NE
Ps
Cerebellar NEP?
Rathke's pouch epithelium
R2
nc ep
lic
R3
NEP
s
ha
Prosencephalic NEP (ventral)
Oral epithelium
Branchial preplacodes
Mandibular arch (I)
avity Oral c
Mandibular arch (I)
R4
(farther from central nervous system)
/phary
Hyoid arch (II)
c ali eph le enc ric mb ent rhorotov p
prosencephalic protoventricle
Optic vesicle
Prose
opt
lic
tegmental/isthma alic lN ph EP ce n se
p pr ro o t s en o v ce en p h tr al ic ic le
(nearer central nervous system)
ha
s
Cephalic preplacodes
es
en
p ce
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
Medullary velum
R5
R6
nx
h III? Arc
Figure 23. A. Continuity between the prosencephalic NEP and the cephalic preplacodes in a GW3.2 embryo. Coronal section. B. Continuity between cephalic preplacodes and branchial preplacodes, by way of the oral epithelium, in a GW3.8 embryo. Sagittal section.
R7?
Arch IV?
449
450 NEP - Neuroepithelium
optic recess
A. GW3.8, C7724
E. GW6.5, C9247 Optic germinal zones
Olfactory placode
Neocortical NEP
Nerve I (olfactory)
Cephalic preplacode
Limbic cortical NEPs Olfactory NEP
See I
B. GW4, C9297
Basal telencephalic NEP
Sprouting nerve I (olfactory)
Basal ganglionic NEP
Optic germinal zones
Olfactory placode Cephalic preplacode
C. GW5, C8966
F. GW7, C1390
prosencephalic superventricle Prosencephalic NEPs
Olfactory NEP
Dorsal Diencephalic NEPs Ventral
Olfactory epithelium
Olfactory nerve reaches prosencephalon optic recess
Olfactory placode
Optic germinal zones
G. GW7.5, C6202 dorsal pool
D. GW5.5, C6516
re
l N E
telencephalic superventricle
P
Ce
bral cortica
telencephalic superventricle
Olfactory NEP?
Olfactory NEP
Basal telencephalic NEP
See J ventral pool
Formative nasal cavity
Olfactory epithelium
foramen of monro
optic recess
Nasal cavity
Optic germinal zones
Scale bars A-D
Scale bars E-G
diencephalic superventricle
451
H. GW6.5, C9247
NEP - Neuroepithelium
Limbic cortical NEP Olfactory NEP
Limbic cortical NEP
telencephalic superventricle
FORMATIVE OLFACTORY BULB
I. GW7.5, C6202
OLFACTORY BULB Olfactory NEP
Nerve I (olfactory)
Olfactory epithelium
Basal telencephalic NEP
Multiple contact points between olfactory nerve and basal telencephalon
Basal telencephalic NEP
telencephalic superventricle
Nerve I (olfactory)
Olfactory epithelium
Multiple contact points between olfactory nerve and basal telencephalon
Figure 24. The time course of the thickening and invagination of the olfactory placode, the formation of the olfactory epithelium (pink), the outgrowth of the olfactory nerve fibers (yellow), and the evagination of the olfactory NEP, at lower (A-G, facing page) and higher magnification (H-I, this page). Sagittal sections.
fying germinal system. Starting as a pluripotent preplacodal germinal matrix, this system gives rise to several faterestricted placodes that, in turn, contribute to the generation of various non-neural components of different cranial organs (eyes, nose, jaws, ears, palate, etc.) as well as to the neurons of the various cranial ganglia that innervate these organs and connect them with specific NEP compartments. This coordinated diversification of the peripheral elements of the head region with complimentary NEP mosaics is exemplified by the development of the rhombomeres, which are distinguished from one another by forming different peripheral and central connections and serving different functions. In this view, neither the different cranial ganglia nor the rhombomere NEPs are reiterated metameric units but are more like the other diversifying NEP mosaics of the CNS, except that they are more conspicuous and short-lived than many other NEP mosaics.
This may be due to a transient role of the rhombomeres in the morphogenesis of the cranial nerve system and their drastic reorganization as the hindbrain develops in higher vertebrates and humans. We speculate that the fleeting presence of rhombomeres 2-7 in higher vertebrates constitutes a recapitulation of a stage of hindbrain evolution in ancestral fish. The rhombencephalic NEP mosaics of fishes, as seen in extant piscine species, produce such hypertrophied structures as the facial lobe, the target of nerve V and VII afferents, the octavolateral lobe, the target of nerve VIII afferents, and the vagal lobe, the target of nerve IX and X afferents (Evans, 1952; Wagner, 2001). However, these paleocephalic central sensory structures, much like the large optic lobe, became reorganized during the phylogeny of higher vertebrates as new neencephalic (forebrain) circuits evolved to process sensory input. Correspondingly, the sensory systems of higher vertebrates and Text continues on page 461
452 C. GW4.5, M2300
Optic vesicle
Cephalic preplacode
Prosen- optic cephalic NEPs
re c
NEP - Neuroepithelium
Developing eye
Dorsal diencephalic NEP
Prosencephalic NEPs
prosencephalic superventricle
open prosencephalic protoventricle
A. GW3.2, M714
ess
Pigment epithelium
Ventral diencephalic NEPs
Lens placode optic recess
Optic germinal zones
anterior neuropore
Retinal NEP
Pituitary placode
(future Rathke's pouch)
B. GW4, C836
Cephalic preplacode
D. GW5, C8314
Future pigment epithelium?
Developing eye
Dorsal diencephalic NEP
Optic germinal zones
prosencephalic superventricle
closed prosencephalic superventricle
Optic vesicle
Pigment epithelium
optic recess Ventral diencephalic NEPs
Future retinal NEP?
Prosencephalic NEPs
Retinal NEP
Lens placode Pituitary placode
(future Rathke's pouch)
All scale bars = 0.25 mm
Cephalic preplacode
optic recess
Pituitary placode
Maxillary process
(future Rathke's pouch)
Maxillary placode
Invaginating lens placode
453 ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
E. GW6, M2161
Developing eye
Migrating lateral preoptic neurons Preoptic NEP
Sclera/cornea
diencephalic superventricle
Anterior hypothalamic NEP
Lens Optic nerve GEP Vi
Choroid fissure
t re
ous
body
Migrating anterobasal nuclear neurons Pigment epithelium Retinal NEP intraretinal space (optic recess)
F. GW7, M2155 (serial sections of eye only) (1) Approximate section 190
Retinal ganglion cells absent (most distant from exiting optic nerve)
(3) Section 164
Lens
(equatorial cut)
ou
(most plentiful near sprouting optic nerve)
Retinal NEP
sb
Choroid fissure
Epithelial cells Fiber cells
Vi t r e
Pioneer retinal ganglion cells
od
y
Crystallin protein
(site of optic nerve sprouting)
(2) Section 178 Retinal ganglion cells
intraretinal space (optic recess) Pigment epithelium
Glial channels adjacent to Retinal NEP?
(fewer due to greater distance from optic nerve exit)
Figure 25. Time course of the development of some components of the eye. Already evaginated when the anterior neuropore closes at GW3.2 (A, facing page), the optic vesicle interacts with the cephalic prepladode to differentiate a lens placode opposite the future retinal NEP on GW4 and GW4.5 (B, C, facing page); the lens placode invaginates on GW5 (D, facing page). Development of the crystalline lens is well underway by GW6 (E, this page) as well as the differentiation of the optic germinal zones into the retinal NEP, the pigment epithelium, and the optic nerve GEP. Pioneer ganglion cells and optic nerve fibers emerge by GW7 (F, this page). Coronal sections.
All scale bars = 0.25 mm
454 A. GW3.8, C7724
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
D. GW5.5, C6516 diencephalic superventricle
prosencephalic protoventricle
Hypothalamic NEPs
Prosencephalic NEPs
Lamina terminalis?
Pituitary placode
Lamina terminalis Rathke's pouch (primordium of anterior pituitary)
(future Rathke's pouch)
Cephalic preplacode
Oral cavity
B. GW4, C9297
E. GW6.5, C9247 diencephalic superventricle
Posterior pituitary GEP
Hypothalamic NEPs
prosencephalic superventricle
Anterior
Hypothalamic NEPs
Pituitary placode
Lamina terminalis Preoptic NEP
(future Rathke's pouch)
Lamina terminalis
Middle
Rathke's pouch (primordium of anterior pituitary)
Oral cavity
Cephalic preplacode
C. GW5, C8966
F. GW7, C1390 diencephalic superventricle Hypothalamic NEPs Preoptic NEP
diencephalic superventricle
Middle
Posterior pituitary GEP
Hypothalamic NEPs
Anterior
Preoptic NEP Lamina terminalis
Lamina terminalis
Rathke's pouch (primordium of anterior pituitary)
All scale bars = 0.25 mm
Oral cavity
Rathke's pouch (primordium of anterior pituitary)
455 G.
diencephalic superventricle
GW6 M2161 (anterior)
Pia
(hypothalamic pool)
Lateral
Hypothalamic neuroepithelium
Middle
Subpial fiber layer Migrating hypothalamic neurons
Arcuate nuclear?
Median eminence
Anterior pituitary epithelium
Pituitary gland primordium
intraglandu
la
r cl eft
Sella turcica of sphenoid bone
Intermediate pituitary epithelium
H.
diencephalic superventricle
GW6 M2161 (posterior)
Pia
(hypothalamic pool)
Subpial fiber layer
Lateral
Hypothalamic neuroepithelium Middle
Migrating hypothalamic neurons
Arcuate nuclear?
Pituitary gland primordium Anterior pituitary epithelium
Sella turcica of sphenoid bone Posterior pituitary glioepithelium (pituicyte precursors)
Figure 26. Time course of the development of the anterior and posterior parts of the pituitary gland. In GW3.8, GW4.0, and GW5.0 embryos (A-C, facing page), the pituitary placode folds in and fuses to form Rathke’s pouch on GW5.5 (D, facing page), the primordium of the anterior pituitary gland. Continuity between the pituitary placode-derived anterior pituitary gland and the hypothalamic NEP-derived posterior pituitary gland is established in the GW6.5 and GW7.0 embryos (E, F, facing page). Sagittal sections. The contiguity between the anterior and posterior pituitary glands is illustrated at a higher magnification in a GW6.0 embryo (G, H, this page). Coronal sections.
456
GW5 Sagittal, CR 7.1 mm, C8966 A.
Cerebellar NEP
Slide 8, Section 2
Upper rhombic lip
Lower rhombic lip Medullary velum
rhombencephalic superventricle (future fourth ventricle)
R2
R4
R3
R5
R7
R6 Otic vesicle
Boundary caps Ganglion VIII (vestibulocochlear)
Epithelium Lumen Arch IV?
Branchial placodes
Developing eye
Lower medullary NEP
Spinal NEP
intraretinal space
Retinal NEP Lens Pigment epithelium
Hyoid arch (II)
Ganglion X (inferior)
Arch III
Anteri o
Mandibular arch (I)
Choroid fissure
r c ar
Ganglion X placode?
Sympathetic trunk ganglia Dorsal root ganglia
dina l vei n
Lateral nasal process
Heart primordium
Olfactory (cephalic) placode
Spinal nerve (dorsal root)
Parasympathetic intramural (cardiac) ganglion? Spinal nerve (ventral root)
Slide 8, Section 8
Cerebellar NEP
B.
Pontine and medullary NEPs
R2 R3
Anterior cardinal vein
Ganglion V (trigeminal)
Boundary caps
Ganglion X (superior)? Nerve IX (glossopharyngeal) Nerve X (vagal)?
Ganglion IX (inferior)
Ganglion VIII (vestibulocochlear)
Migrating ganglionic neurons?
X
th
Heart primordium
Parasympathetic intramural (cardiac) ganglion?
nglia nk ga
Ganglion X placode in Arch IV
ru c t
Ganglion X (inferior)
eti
Hyoid arch (II)
pa
Mandibular arch (I)
m
IX
Ganglion IX placode in Arch III Lateral nasal process
Nerve XI (spinal accessory)?
Sy
Maxillary/ mandibular placode Maxillary process
R7
R6
Ganglion VII (facial)?
Nerve V (sprouting opthalmic branch) Nerve V (sprouting maxillary branch)
Developing eye
R4
R5
Lower medullary NEP
Dorsal root ganglia
457
C.
Upper rhombic lip
Medullary velum
Lower rhombic lip
Cerebella r NE P
Slide 8, Section 14
FONT KEY: ABBREVIATIONS: ventricular divisions - capitals NEP - Neuroepithelium Germinal zone - Helvetica bold R - Rhombomere Transient structure - Times bold italic Permanent structure - Times Roman or Bold PROPOSED RHOMBOMERE IDENTITIES R2
Pontine and medullary NEPs
R2
R3
R5
R4
R3
R6
R7
Nerve X boundary cap and nerve roots
Ganglion VIII (vestibulocochlear) Ganglion V (trigeminal)
Nerve V (sprouting maxillary branch)
Otic vesicle
R4
Ganglion IX (superior) Ganglion X (superior)
Ganglion VII (facial)
R5
Nerve X (vagal) Ganglion IX (inferior)
Sy
m
pa
R6
t
h
Maxillary/ mandibular placode
Ganglion IX placode Branchial placodes in arch III?
runk ganglia ic t
The placodal epithelium separated from the mesenchyme is an artifact of histological processing.
et
Hyoid arch (II)
Maxillary process
Ganglion X (inferior)
Heart primordium
D.
RHOMBOMERE/GANGLION RELATIONSHIPS R2
Upper rhombic lip
Slide 8, Section 20
Lower rhombic lip
R3
R2 Ganglion V (trigeminal)
R4 Otic canal (marks the initial invagination from the embryonic surface)
Ganglion VIII (vestibulocochlear)
R5
Otic vesicle Ganglion VII (facial)
R6
Sy
Heart primordium
R7 t
Ganglion X (inferior)
runk ganglia ic t
Hyoid arch (II)
Ganglion V placode?
pa
Axons from the trigeminal ganglion enter the brain here. Axons from the facial ganglion (VII) enter the brain at the junction between R3 and R4. Vestibulocochlear ganglionic (VIII) axons enter the brain here. The otic vesicle touches this part of the brain. Axons from the glossopharyngeal ganglia (IX superior and inferior) enter the brain here. Axons from the vagal ganglia (X superior and inferior) enter the brain here.
et
Mandibular arch (I)
Maxillary process
m
h
Ganglion VII placode?
Nerve V (sprouting mandibular branch)
R7
Trigeminal NEP - germinal source of the central trigeminal nuclei except the mesencephalic nucleus. Facial NEP - germinal source of facial motor and sensory receptor neurons of the facial (VII) ganglion. Vestibulo-auditory NEP germinal source (with R5) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Vestibulo-auditory NEP germinal source (with R4) of central auditory nuclei and vestibular nuclei, except the cochlear nuclei. Glossopharyngeal NEP germinal source of sensory neurons that receive input from the glossopharyngeal (IX) ganglion. Vagal (X) sensory NEP germinal source of the dorsal sensory nucleus and other sensory vagal nuclei.
Figure 27. Serial sagittal sections, from medial (A) to lateral (D), through the head and neck region of a GW5.0 embryo (facing page and this page). They illustrate the vertical alignment and contiguity between cranial ganglia V, VII, VIII, IX, and X, and rhombomeres R2, R3, R4, R5, R6, and R7, respectively. The spatial relationship of the cranial ganglia and the maxillary process, the mandibular arch (I), the hyoid arch (II), and arches III and IV are also visible.
GANGLION/PLACODE RELATIONSHIPS V
Derived from a placode at the junction of the maxillary process and mandibular arch. VII Derived from a placode in the hyoid arch. VIII Both the vestibular and spiral ganglia are derived from the otic vesicle epithelium. IX The inferior and possibly most of the superior ganglionic neurons are derived from a placode in arch III. X The inferior and possibly most of the superior ganglionic neurons are derived from a placode in arch IV.
458 FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
A.
GW5 Sagittal, C8966 Slide 8, Section 2
Developing eye Lateral nasal process intraretinal space
Pigment epithelium
Retinal NEP
Nerve I (sprouting)
Nerve V (sprouting opthalmic branch)
Lens
Olfactory placode
Nerve V (sprouting maxillary branch)
Choroid fissure
Ganglion V (trigeminal)
Maxillary process
B.
GW5.5 Sagittal, C6516 Slide 20, Section 14
Cerebral cortical NEP
Maxillary/ mandibular placode
Nerve V (sprouting mandibular branch) Mandibular arch (I)
telencephalic superventricle
Developing eye intraretinal space
Basal ganglionic NEP
Retinal NEP
Pigment epithelium
Nerve V (sprouting opthalmic branch)
Lateral nasal process
ar NEP rebell Ce
Choroid fissure
Dorsal rhombic lip
Ganglion V (trigeminal)
Nerve V (sprouting maxillary branch)
R2 Pontine NEP
Maxillary process
Medullary velum
Maxillary/ mandibular placode
Nerve V (sprouting mandibular branch)
Hyoid arch (II)
Anterior cardinal vein
Mandibular arch (I) Figure 28. A. Far-lateral section from the opposite side of the preceding GW5.0 embryo, to show the relationship between the three prongs of the trigeminal ganglion and the developing eye, the maxillary process, and the mandibular arch. B. Sprouting fibers of the ophthalmic, maxillary, and mandibular branches of the distal trigeminal nerve in a GW5.5 embryo. Sagittal sections.
rhombencephalic superventricle
Ventral rhombic lip
Ganglion VIII (vestibulocochlear)
Otic vesicle Lumen
Epithelium
459 GW5.5 Sagittal, C6516 A. Slide 6, Section 11
R2
Nerve V boundary cap
R4
Tr i
Nerve V (opthalmic branch)
ABBREVIATIONS: NEP - Neuroepithelium R - Rhombomere
R5
ge mi
Pigment epithelium
na
ga
l
Intraretinal space
EYE
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
rhombencephalic superventricle
nglion (V)
Retinal NEP
Trigeminal afferent fibers
VIII afferent fibers
Nerve VIII boundary cap
Vestibulocochlear ganglion (VIII)
Anterior cardinal vein Facial ganglion (VII)?
Choroid fissure
Superior glossopharyngeal ganglion (IX)
Lumen Epithelium
Otic vesicle
B.
Slide 7, Section 6
R2
Nerve V boundary cap Tr g a ig e m ng i (V lionnal )
Nerve V
rhombencephalic superventricle
R3
R4
R5
R6
R7
VII + VIII afferent fibers Glossopharyngeal afferent fibers
Vestibulocochlear ganglion (VIII)
Vagal afferent fibers
rv
e I X
Maxillary process
Ne
Superior vagal ganglion (X)
X Ne rv e
Figure 29. A. Entry of afferents of the trigeminal ganglion into R2, and of the vestibulocochlear ganglion into R4 and R5. B. Entry of afferents of the glossopharyngeal ganglion into R6 and of the vagal ganglion into R7. Sagittal sections from a GW5.5 embryo.
Mandibular arch (I)
Inferior glossopharyngeal ganglion (IX)
Migrating IX ganglionic neurons? Hyoid arch (II)
Placodal germinal source of ganglion IX?
Arch III Inferior vagal ganglion (X)
460 GW6.5 Sagittal, C9247 A. Slide 16, Section 13
Pontine NEP VIII afferent fibers
V afferent fibers Nerve V boundary cap
Nerve VIII boundary cap Otic vesicle
Nerve V (trigeminal)
epithelium
Nerve VIII (vestibulocochlear)
Vestibulocochlear ganglion (VIII)
Trigeminal ganglion (V)
B. Slide 18, Section 13
Medullary NEP
X afferent fibers
IX afferent fibers
Nerve IX (glossopharyngeal)
Nerve IX boundary cap
NEP - Neuroepithelium
FONT KEY: Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Bold
Nerve X (vagus)
Nerve X boundary cap
Figure 30. A. Penetration of trigeminal and vestibulocochlear afferents into the pons (former R2 and R4-R5). B. Penetration of glossopharyngeal and vagal afferents into the medulla (former R6 and R7). Sagittal sections from a GW6.5 embryo.
461 humans become reorganized during ontogeny. An example may be the necessary reorganization of the octaval system of aquatic fish, which have a lateral line organ but lack a cochlea, into the cochlear system of land vertebrates. The innervation of this complex tonotopically organized auditory system required profound reorganization of the auditory system in terrestrial vertebrates. Indeed, the neurons of the dorsal and ventral cochlear nuclei do not derive from the rhombomeres but from a new germinal system, the cochlear NEP and EGL located in the region of the lower rhombic lip. Passing from hypothetical phylogeny to empirically based observations, we may summarize the differences between the development of the spinal cord and the brain as follows. First, unlike the segmented mesodermal somites in the trunk region, the head mesoderm is unsegmented. Second, whereas the neural crest-derived and somitedependent spinal ganglia are reiterated structures, the branchial arches, the diversifying olfactory, optic lens, and pituitary placodes, and the trigeminal-facial, otic, and glossopharyngeal-vagal placodes and ganglia derived from them are not reiterated structures but functionally diverse systems. Third, while there is no hint of any longitudinal (rostrocaudal) metameric compartmentation either in the spinal NEP or the differentiating components of the spinal cord gray matter (although there is a pronounced dorsoventral compartmentation), there is, in contrast, a marked compartmental heterogeneity in the brain vesicles. This is marked at the outset by the presence of variegated NEP mosaics of different sizes and shapes both in the hindbrain and the forebrain. Finally, since these NEP regions—e.g., the NEPs of the different thalamic nuclei and the different areas of the cortex—become linked to the periphery much later (after synaptic connections are established with the primary afferents and the lower motor neurons), their diversification cannot be attributed to periphero-central signaling mechanisms but must be due to either endogenous regulation and/or centro-central signaling processes. Endogenous Genetic Regulation in NEP Cell Diversification. While in conventional histological preparations individual NEP cells look alike throughout the neuraxis, the NEP matrix consists of morphologically dissimilar NEP compartments from the beginning. The configuration and cellular dynamics of these NEP compartments— those of the rhombencephalon, mesencephalon, diencephalon and telencephalon—are quite different from the outset, and so are the different classes and varieties of neurons and brain structures they generate. While the dome-like expanse of dorsal telencephalic NEP matrix, for instance, generates an immense number of relatively homogeneous classes of neocortical neurons, the variegated ventral telencephalic NEP matrix produces a much greater variety of neurons for such diverse brain structures as the septum, the basal telencephalic nuclei, the basal ganglia, the amygdala, etc.—each with its own neurogenetic timetable, pop-
ulation size, and cell composition. The same applies to the variegated diencephalic and mesencephalic NEP compartments. And as development progresses, the larger NEP matrix divisions become subdivided into a series of bilaterally symmetrical smaller protuberances, cavities, and discontinuous stretches and patches marked by different cell depth and cell packing density. In our earlier experimental studies in rats, we used 3H-thymidine autoradiography to date the changing spatial and temporal dynamics of cell proliferation in many of these NEP mosaics, track the migratory paths and settling patterns of the tagged neurons, and correlate these data with the chronology of neurogenesis in various structures of the mature brain. Based on that information, we named the identified NEP mosaics by their putative target structures. Thus, we have such divisions as the neocortical, limbic-cortical, and basal ganglionic NEPs in the early telencephalon; the thalamic, subthalamic, and hypothalamic NEPs in the early diencephalon; and the tectal and tegmental NEPs in the early mesencephalon. And as embryonic development progresses, most of these early NEP compartments become partitioned into smaller components, such as the tectal NEP into the superior collicular and inferior collicular NEPs, the tegmental NEP into the NEPs of the red nucleus, oculomotor nuclei, substantia nigra, etc. We illustrate this progressive NEP matrix compartmentation at a select coronal level of the human prosencephalon which begins with three diencephalic divisions—the all-thalamic, all-subthalamic and allhypothalamic—and each of which becomes subsequently divided into smaller NEP mosaics (Figure 31). The fact that dissimilar proliferative and differentiation dynamics are expressed by many NEP compartments—e.g. cortical, basal ganglionic, hippocampal, thalamic, etc.— that have no direct peripheral connections suggests that their diversification is due not to exogenous signaling but to endogenous signaling. (Although we postulate that the superventricles and the superarachnoid reticulum influence NEP cell proliferation and differentiation, respectively, their diffuse or global influences cannot explain the local diversification of NEP cells.) The inference that the germinal cells forming certain NEP compartments are intrinsically different is supported by genetic studies that are currently carried out in mice and other experimental animals. For instance, it has been reported that Pax6 is expressed by NEP cells throughout the prosencephalic neural plate before it folds and fuses (Inoue et al., 2000); thereafter, Pax6 expression persists in the dorsal telencephalic NEP but vanishes from the ventral telencephalic NEP (Stoykova et al., 2000). Six3 (Oliver et al., 1995) and retinoic acid expression (Mic et al., 2004; Halilagic et al., 2006; Ribes et al., 2006) have been implicated in the early phases of prosencephalic development. The dorsal telencephalic NEP cells that are destined to generate cortical neurons also express the transcription factors Emx1 and Emx2, whereas the ventral NEP cells destined to generate basal ganglionic neurons express Nkx2.1, Dlx1, Dlx2, and Gsh2 (Torreson et Text continues on page 465
462 A. GW3.2, M714 diencephalic protoventricle
0.25 mm
B. GW4.5, M2300 expanding diencephalic superventricle
Optic germinal zones optic recess
Lens placode Optic nerve GEP? Cephalic preplacode
C. GW5.5, M1000 Pretectal (mesencephalic) NEP
Stockbuilding diencephalic NEPs
Allhypothalamic NEP
Cephalic preplacode
Retinal NEP
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Allsubthalamic NEP
Optic germinal zone
Pigment epithelium
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic
Allthalamic NEP
mesencephalic superventricle
thalamic pool
Migrations
Thalamic Subthalamic Hypothalamic
Stockbuilding diencephalic NEPs begin to partition
Thalamic NEP (evaginating)
Figure 31. Progressive NEP matrix compartmentation, cell migration, and cell differentiation in the developing human diencephalon between GW3.2 (A) and GW8.0 (G) on this page, the facing page, and the following overleaf. The original NEP divisions – the Subthalamic all-thalamic, all-subthalamic and NEP all-hypothalamic – become (thickening) subdivided into smaller, faterestricted mosaics (marked by Hypothalamic asterisks) that generate NEP neurons for different nuclei (evaginating) (most of them not identified). The process is temporally associated with 0.25 mm the expansion and shrinkage of the diencephalic superventricle (blue) and the superarachnoid reticulum (yellow). Coronal sections.
Thalamic NEPs (evaginating and stockbuilding)
expanding diencephalic superventricle
Thalamic NEPs
(thinning by unloading neurons)
Superarachnoid reticulum Optic germinal zones
subthalamic pool
by unloading neurons)
Pigment epithelium intraretinal space (optic recess)
Retinal NEP
Subthalamic NEPs (thinning
hypothalamic pool
Hypothalamic NEPs (thinning by
unloading neurons)
Onset of subthalamic and hypothalamic parenchymal expansion 0.25 mm
Partitioning of diencephalic NEPs continues
463 D. GW6.5, M2051 Pretectal (mesencephalic) NEP
mesencephalic superventricle
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Thalamic NEPs expanding thalamic pool
diencephalic superventricle Cerebral cortical NEP
(stockbuilding, some neuronal unloading)
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium
Migrations
Thalamic NEP
Thalamic Subthalamic Hypothalamic
(thinning by unloading neurons)
Superarachnoid reticulum
expanding telencephalic superventricle
shrinking subthalamic pool
Amygdaloid NEP
shrinking hypothalamic pool
Optic germinal zones
All diencephalic NEPs continue to partition
Subthalamic NEPs (thinning by unloading neurons)
Optic nerve GEP
Hypothalamic NEPs
Pigment epithelium
(thinning by unloading neurons)
Retinal NEP Optic tract and chiasm
optic recess
Optic nerve GEP
pineal recess
E. GW7, M2155
Partitioning thalamic NEPs
(stockbuilding, more neuronal unloading)
diencephalic superventricle Cerebral cortical NEP
0.5 mm
Thalamic NEP expanding thalamic pool
(thinning by unloading neurons)
Onset of thalamic parenchymal expansion
expanding telencephalic superventricle
shrinking subthalamic pool
Amygdaloid NEP
Subthalamic NEPs shrinking hypothalamic pool
(thinning by unloading neurons)
Hypothalamic NEPs (thinning by unloading neurons) 0.5 mm
Figure 31 continues.
464 F. GW7.5, C8553
FONT KEY: ventricular divisions - capitals Germinal zone - Helvetica bold Transient structure - Times bold italic Permanent structure - Times Roman or Bold
Choroid plexus
Cerebral cortical NEP
ABBREVIATIONS: GEP - Glioepithelium NEP - Neuroepithelium SVZ - Subventricular zone expanding telencephalic superventricle
Migrations
Thalamic NEPs
Thalamic Subthalamic Hypothalamic
(thinning by unloading neurons)
Fornical GEP Choroid plexus
Subthalamic NEPs (thinning
by unloading neurons)
Amygdaloid NEP
shrinking diencephalic superventricle
Hypothalamic NEPs (thinning by unloading neurons) Superarachnoid reticulum
Trigeminal ganglion (V)
Parenchymal expansion due to extensive neuronal migration from the NEPs continues in the diencephalon
1 mm
G. GW8, C609
expanding telencephalic superventricle
Choroid plexus
Fornical GEP
Migrating dorsal complex and periventricular complex neurons?
Ganglionic NEP and SVZ Cerebral cortical NEP
C aud
THALAMUS
shrinking diencephalic superventricle
AMYGDALA
SUBTHALAMUS
a te
Thalamic NEPs
(depleted of most neuronal stem cells)
Internal capsule (contains axons from thalamic neurons entering cerebral cortex)
Subthalamic NEPs (depleted of most neuronal stem cells)
HYPOTHALAMUS Amygdaloid NEP
Diencephalic parenchymal expansion is primarily due to axonogenesis and dendrogenesis rather than to the addition of new neurons from the NEP
Hypothalamic NEPs (depleted of most neuronal stem cells)
Migrating mammillary body neurons
1 mm
Figure 31 concludes.
465 al., 2000; Wilson and Rubenstein, 2000; Yun et al., 2001; Corbin et al., 2003; Muzio and Mallamaci, 2003). Similarly, Ngn1 and Ngn2 are expressed in the dorsal telencephalic NEP, whereas Mash1 is expressed in the ventral telencephalic NEP (Ma et al., 1997; Fode et al., 2000; Parras et al., 2002). It has also been reported that Emx2 expression in the rodent cortical NEP shows a high-caudal to low-rostral gradient, and a high-medial to low-lateral gradient (Leingartner et al., 2003). Since these gradients are the opposite of cortical maturation gradients, not only in rodents (Bayer and Altman, 1991a) but also in humans (as illustrated in the preceding Volumes of this Atlas), it may be inferred that Emx2 expression declines as cortical neurogenesis and differentiation progresses. The importance of Emx signaling in dorsal telencephalic development is indicated by observations that cortical development, including that of the hippocampus, is greatly retarded in Emx mutants (Bishop et al., 2003). In light of the importance we attribute to the growth of the fetal telencephalic choroid plexus in cortical development, an interesting aspect of Emx gene action is its suppression of telencephalic choroid plexus development (von Frowein et al., 2006). The production of choroid plexus progenitor cells is apparently associated with Otx2 and BMP7 expression. (The cells of the non-neuronal rhombencephalic choroid plexus are reported to express Lmx1a and Gdf7; Landsberg et al., 2005). Finally, according to a study (Kimura et al., 2005) that has used a different nomenclature from the one we use in this Atlas, Wnt8b expression demarcates the hippocampal primordium in the medial cortex as well as other components of the limbic circuit, including the diencephalic epithalamus and mammillary body. Within the hippocampus, Ephb1 demarcates the ammonic NEP that generates pyramidal cells, Wnt3a the dentate NEP that generates granule cells, and TTR the primordium of the nonneuronal telencephalic choroid plexus. There are currently few studies available regarding the genetics of diencephalic and mesencephalic NEP cell specification. Pax6 is expressed in the diencephalic NEP (Warren and Price, 1997) but not in the mesencephalic NEP where, instead, Pax3 and Pax7 are expressed (Kammermeier and Reichert, 2001). It has been reported that Msx1 genes induce Wnt1 expression at the dorsal midline region of the mesencephalic and diencephalic junction, and in homozygous Msx1 mutant mice several structures fail to develop at this site (Bach et al., 2003). Mash1 is required for the specification of NEP cells that produce the neuroendocrine neurons of the ventral, arcuate, and ventromedial hypothalamic nuclei (McNay et al., 2006). The bHLH transcription factor SCL is expressed in pretectal, midbrain, and hindbrain NEPs but not elsewhere in the CNS (van Eekelen et al., 2003), and the transcription factor Otx2 appears to control neurogenesis and progenitor identity in the midbrain tectum and tegmentum (Vernay et al., 2005). There are more data regarding the genetics of cerebellar development. FGF and Wnt expression are early
events in cerebellar morphogenesis (Morales and Hatten, 2006; Waters and Lewandoski, 2006). Pax6, Math1, Tbr1, and Tbr2 have been implicated in the generation of the NEP cell line that produces cerebellar deep nuclear neurons, and these factors are expressed sequentially as the young deep neurons enter the nuclear transition zone (Fink et al., 2006). Among other transcription factors expressed in this lineage are Otx3-Dmbx1 (Kimura et al., 2005). The Purkinje cell lineage expresses Math1 (Jensen et al., 2004; Wang et al., 2005), Ptf1a (Hoshino, 2006), and Ebf2 (Croci et al., 2006). The cell lineage of the EGL, which gives rise to cerebellar microneurons (see below) and can be visualized with the marker RU49 (Alder et al., 1996), expresses Math1 (Machold and Fischell, 2005) and Zic1 (Aruga et al., 1998). Integrin-linked kinase (ILK) is reported to be a critical agent in the proliferation of granule cell precursors (Mills et al., 2006) and Bergmann glial cell differentiation (Belvindrah et al., 2006). Finally, the transcription factor Zpf423 has been implicated not only in the production of cerebellar granule cells but also in the proliferation of other late-generated precursors in the cerebral cortex and the hippocampus (Alcaraz et al., 2006). In conclusion, there is growing evidence for genetically controlled diversification of some of the NEP mosaics that are not direct targets of exogenous (peripheral) influences. We return later to a third source of morphogenetic regulation, i.e., the centrocentral signaling between developing components of the CNS.
F. Timetables of Neurogenesis There is no direct way to determine the time of origin of neurons in the human CNS. But that can be done indirectly by using the quantitative data obtained in rats with 3 H-thymidine autoradiogaphy. Notwithstanding the great difference in the speed of their development, embryonic (E) days versus gestational weeks (GW), there is a close morphological correpondence between prenatal rat CNS development (E11 to E21) and human CNS development during the first trimester (GW3-GW12). This matching relationship is shown in sagittal sections (Figure 17A, B), anterior coronal sections (Figure 17C, D), and posterior coronal sections (Figure 36A, B). We re-examined this relationship in the material presented in this atlas series by matching sections from the spinal cord and the brain in the two species. Tables of the estimated chronological eqivalence of human CNS neurogenesis with the empriciallybased rat CNS neurogenesis are summarized in the Appendix (page 490). We emphasize that the correpondence is limited to the first trimester and early second trimester in humans. Rats are born at a time equivalent to the early second trimester in humans. After birth on E22/P1, the rat CNS rapidly matures and has an adult appearance by the time of weaning (approximately P21). In contrast, human CNS maturation is stretched out over a long time span through the remaining second trimester, the third trimester, and even into the early postnatal years.
466 G. Cell Migration, Sojourn Zones, Secondary Germinal Matrices, and Fate-Restricted Glioepithelia Cell Migration and Migratory Streams. Following the production of neurons, cell migration is one of the most important mechanisms in the morphogenetic organization of the developing and maturing CNS. Cell migration is a very complex and regionally diversified process. There are small cohorts and large streams of migrating neurons; short-distance and long-distance migrations; and migrations with a straight path or a tortuous route. Some young neurons migrate through interstitial tissue, like the precerebellar neurons that form the inferior olive (Altman and Bayer, 1987b); others migrate beneath the pia, like the neurons of the posterior extramural migratory stream that produce the neurons of the pontine gray (Altman and Bayer, 1987d); still others migrate in a subventricular position, like the rostral migratory stream (RMS) of the telencephalon that conveys neurons to the olfactory bulb (Altman, 1969; Luskin, 1993). While most migrations are ipsilateral, there are also some that are contralateral, i.e., the neurons of the precerebellar extramural migratory stream that form the lateral reticular and external cuneate nuclei (Altman and Bayer, 1987c). The simplest form of cell migration is the short-distance radial translocation of a cohort of young neurons from a NEP mosaic to a nearby parenchymal destination. This mode of migration, often at a right angle to the NEP matrix, is known as radial migration. It is a widespread phenomenon during early embryonic development throughout the CNS before the expanding parenchyma becomes filled with aggregates of cell bodies and crisscrossing fiber tracts that obstruct the path of migrating neurons toward their final destination. For instance, in the developing cerebral cortex, the earliest Cajal-Retzius neurons migrate radially to the primordial plexiform layer (Figure 32A, B) before the cortical plate begins to form (Figure 32C). As Golgi studies have shown, these cells have a trailing process in the NEP and a leading process approaching the pial surface (Morest, 1970). Although radial migration has been attributed to guidance by “radial glia” (see Section B, page 428), a far more likely or prevalent mechanism is perikaryal (or somal) translocation (Berry and Rogers, 1965; Morest, 1970; Nadarajah et al., 2003; Hatanaka et al., 2004). As we noted earlier, nuclear translocation within the spindleshaped cytoplasm is a fundamental property of NEP cells that shuttle to and from the ventricular lumen to undergo mitotic division. The nuclei of young neurons leaving the NEP matrix may similarly translocate inside the cells’ radially extending neurite. (Such a process of nuclear translocation has been well documented for granule cells in the cerebellar cortex; e.g., Altman and Bayer, 1997). However, radial migration is only one of the many forms of neuronal locomotion. For instance in the developing cerebral cortex, the translocating young neurons interrupt their radial migration and interact with various fiber systems.
The cells and fibers undertake a choreographed series of movements to form different layers in what we have called the stratified transitional field or STF (Figure 32D). The evidence that clonally related cells disperse widely in the developing cerebral cortex (Walsh and Cepko, 1992; Mathis and Nicolas, 2006) indicates that cells may migrate both radially and non-radially (tangentially) within the same brain region (Bayer et al., 1991a, b). Tangential migration is better accounted for by an amoeboid form of locomotion rather than perikaryal translocation, with the philopodia of a neuron’s leading process sampling the local milieu or responding to distal signals, and determining the direction of cell progression in one or another direction. Radial translocation at a right angle from the NEP matrix to the surface of the cortex is obviously a simpler task than the guidance of tangential migration to some distant site that may require multiple navigation cues. Cell polarization, guidance by attractive and repulsive forces in the immediate vicinity of the moving cell, and long-range signaling by molecular diffusion gradients have been postulated to act as directional biases, signposts, and beacons. However, little is currently known about their exact nature. Filamin-A has been implicated in the control of the shape of migrating cortical neurons and their direction of migration (Sato and Nagano, 2005). The subpial Cajal-Retzius cells of the primordial plexiform layer secrete reelin, a large extracellular matrix protein. Reelin has been implicated as a signaling factor in the columnar (vertical) and laminar (horizontal) organization of cortical cells (Ogawa et al., 1995; Nishikawa et al., 2002). The absence of reelin in mutant mice results in abnormal cell migration and cell lamination not only in the cerebral cortex but also in the hippocampus, the cerebellum (D’Arcangelo et al., 1995), the olfactory bulb (Hack et al., 2002), and some hindbrain nuclei (Rossel et al., 2005). In the developing human cerebral cortex, reelin expression is present in the primordial plexiform layer by GW7 to GW8 (Zecevic et al., 1999) and somewhat later in the hippocampus (Abraham et al., 2004). Among other factors that appear to play a role in the migration and settling of cortical neurons is Cdk5 (Hammond et al., 2004), presenilin-1 (Louvi et al., 2004), COUP-TF nuclear receptors (Tripodi et al., 2004), and GABA(B) receptors (Lopez-Bendito et al., 2003). The properties of the rostral migratory stream (RMS) associated with the forebrain subventricular zone (SVZ), which forms prenatally in animals (Pencea and Luskin, 2003) and humans (Volume 4 of this Atlas), but persists through adulthood, has received considerable experimental scrutiny recently (though mostly in postnatal animals). In the human forebrain, the RMS is recognizable as a distinct entity by GW11, and it expands greatly during the second and third trimesters (Volumes 2-3 of this Atlas). In adult rats, progenitor cells stream in this glia-encased tube (Peretto et al., 1997) and supply not only microneurons (granule cells) to the olfactory bulb but also neuroglia Text continues on page 468
467
A.
Migrating Cajal-Retzius cells
GW6.5 M2155
Primordial plexiform layer Cerebral cortical NEP
Settling Cajal-Retzius cells Migrating subplate neurons
B.
GW7.5 M2042
Primordial plexiform layer
Horizontally-aligned Cajal-Retzius cells
C.
Vertically-aligned subplate neurons
NEP Layer I Cortical plate
GW8 C9226
(STF 1) (STF 5)
NEP Cajal-Retzius cells
D.
GW8.5 M2050 Delaminating subplate neurons
Layer I Cortical plate
STF 1
STF 5
NEP Figure 32. Onset of the parenchymal development of the neocortex. The first differentiating neurons to leave the neocortical NEP, at about GW6.5, are the Cajal-Retzius cells (A), followed by the subplate neurons at about GW7.5 (B). The cortical plate begins to form, at the site illustrated, at about GW8.0 (C), and the first two layers of the stratified transitional field (STF) at about GW8.5 (D). (Modified Figure 9 from Altman and Bayer, 2002.)
468 (Aguirre et al., 2002; Fukushima et al., 2002). The proliferating SVZ cells and the migrating RMS cells express the microtubule associated protein, doublecortin (Yang et al., 2004) and stathmin (Jin et al., 2004). The homeobox gene Vax1 (Soria et al., 2004) and nitric oxide (Moreno-Lopez et al., 2004) were found to exert an inhibitory influence on SVZ and RMS cell proliferation, and integrin and laminin have been implicated in the migration of RMS cells (Emsley and Hagg, (2003). Slit1 and Slit2, repellents of neurite growth secreted by cells of the septum bordering the RMS stream, exert a guiding influence on migrating RMS cells (Nguyen-Ba-Charvet et al., 2004). In contrast to the RMS, relatively little is known about the guidance mechanisms of the unique migratory stream of neurons that form the precerebellar nuclei (Altman and Bayer, 1997). The progenitors of olivary neurons (the source of climbing fibers) that migrate in the posterior intramural migratory stream express Math1. Netrin1 is involved in the migration of inferior olivary neurons (Bloch-Gallego et al., 1999; Alcántara et al., 2000; de Diego et al., 2002). The pontine neurons (a source of mossy fibers) that migrate in the anterior extramural migratory stream express Ngn1, and their migration is abnormal in mutant mice lacking the chemokine receptor CXCR4 (Vilz et al., 2005). The precerebellar nuclei are absent or disorganized in netrin1 homozygous mutant mice (Kubota et al., 2004). As in the rat, the precerebellar migratory streams are also prominent in the developing human CNS. The posterior intramural migratory stream begins to form by GW6.5-GW7.0 (this Volume) and the expanding inferior olive is evident by GW7.5 (Volume 4 of this Atlas; Bayer and Altman, 2006). The anterior extramural migratory stream is not recognizable until GW9 and the pontine gray nucleus starts to form about GW11, at about the same time that the earliest descending corticofugal fibers begin to traverse it. Transitional Fields and Sojourn Zones. We have illustrated during the second trimester (Volume 3 of this Atlas; Bayer and Altman, 2005) the prominence of the cortical transitional stratified field (STF) situated between the NEP
and the expanding cortical plate, the future gray matter. We identified six cellular and fibrous layers within the STF, distinct strata where cortical neurons sojourn for some time and mingle with afferent, efferent, and commissural fibers before they resume their migration and settle in the cortical plate. We postulated that the STF is a staging area where connections form between the topographically unspecified sojourning cortical neurons and the somatotopically, tonotopically and retinotopically specified thalamocortical afferents that provide input to them. The STF begins to form in the earlier-maturing anterolateral cortical region, and it spreads slowly dorsally and medially. Where present, the STF consists initially of two layers, the fibrous STF1, and the cellular STF5 (Figure 32D). By GW10, the bilayered STF is present throughout the anterior cortex, and it is evident that STF5 is composed of sojourning young cortical neurons that have left the NEP, and STF1 is the target of thalamocortical afferents that have crossed over from the diencephalon into the telencephalon in the internal capsule (Figure 33A). Between GW9 and GW11 an additional layer, STF4, begins to emerge slowly and uncertainly in the earlier maturing lateral aspect of the neocortex. The emergence of STF4 may be associated with the onset of the descent of corticofugal fibers. The other STF layers (STF3, STF2, and STF6) begin to form thereafter and all six of the STF layers are present by GW13.5 (Figure 33B). By the latter age, there is also a clear difference in the organization of the STF in the future motor cortex anteriorly and the future sensory cortex posteriorly. STF5 is best developed in the motor areas (Figure 34A) and STF3 is a unique feature of the sensory areas (Figure 34B). The different cytological organization of STF in the motor cortex and visual cortex is illustrated at higher magnification in a GW20 fetus (Figure 35). In the visual cortex, STF3 is composed of three sublayers (the honeycomb matrix). We hypothesize that the trilaminar STF3 contains sojourning neurons that will form the granular layer (layer IV), the principal target of thalamocortical afferents, and the STF5 contains sojourning neurons that will form the pyramidal layer (layer V), the source of corticospinal efferents.
Text continues on page 472
469
Layers of the stratified transitional field
B. GW13.5, Y144-63
E AL N P+SVZ IC
CO R
L CA TI
COR T
L PLATE ICA T R
E AT PL AL IC ATE RT BPL CO SU
CO
A. GW10, Y1-59
Z
5
Choroid plexus
1
SV P+ NE
Choroid plexus
Ammon's horn Dentate gyrus
Hippocampus (ammon's horn)
6
Hippocampus
ate ud a C
THALAMUS n
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STRIATAL NEP+SVZ
THALAMUS
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Int
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ix Forn
ix rn Fo
STRIATAL NEP+SVZ
5
4
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Amygdala
ral reb e Ce duncl pe
Optic tract
te
Caudate
rn
al
ca
ps
ul
e
Amygdala
Figure 33. Increase of the STF from two layers in the GW10 fetus (A) to six layers in the GW13.5 fetus (B). Coronal sections. (Modified Figure 8 in Altman and Bayer, 2002.)
470
GW13.5 CORONAL, Y144-63 Cort
A.
ical plate
Subplate
Anterior section of motor cortex
CORTIC
PARACENTRAL LOBULE
AL
1 NE P
+S
2
4 5
VZ
Choroid plexus
Lateral ventricle um
NE
llos
TR
Hippocampal commissure
S
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u Ca
da
te
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f c o rp u s c a
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IA TA L
Ea rly fib e
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SEPTUM
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Posterior section of sensory cortex
3
4 5
rti
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PARIETAL LOBE
ca
SUPERIOR COLLICULUS
MIDBRAIN TEGMENTUM
OCCIPITAL LOBE
e lat l p
SVZ P+ NE AL us IC plex RT roid Cho CO
Lateral ventricle
5 4
31
PONTINE GRAY
Figure 34. Regional differences in STF organization in the future motor cortex anteriorly (A) and the future sensory cortex posteriorly (B) in a GW13.5 fetus. Coronal sections. (Modified Figure 11 in Altman and Bayer, 2002.)
471
A. Motor cortex
GW20 Sagittal, Y27-60
Cortical plate
Layer I
B. Visual cortex
Cortical plate
Layer I
Subplate
Subplate
STF
1
STF
STF 2
(STF 2)
1
a STF b c 3
STF
4
STF 4
STF 5 STF 5
STF 6
STF 6
CORTICAL NEP+SVZ
CORTICAL NEP+SVZ
Figure 35. Regional differences in STF organization in the motor cortex (A) and the visual cortex (B) in a GW20 fetus (specimen #5, Volume 4, Bayer and Altman, 2005). Note the thickness of STF4 in the developing motor cortex and the complex organization of STF3, with the honeycomb matrix, in the developing visual cortex. Sagittal sections. (Note the scale differences between A and B; the motor cortex is much thicker than the visual cortex at this stage.)
472 Like the developing cerebral cortex, the developing cerebellar cortex has transitional fields and sojourn zones. In contrast to the cerebellar NEP of the rat, which has only two divisions, C1 and C2 (Figure 36A), the primordia of the medial vermis and a single (“intermediate”) hemisphere, the human cerebellar NEP also has a true “lateral” or neocerebellar division, identified as C3 (Figure 36B). Surrounding these three NEP divisions are complex migratory and sojourn zones, the cerebellar transitional field (CTF). As seen in a GW6.5 embryo (Figure 37), CTF1 is a superficial fibrous layer, CTF2 consists mostly of tangentially migrating early generated neurons, CTF3 is an inner fibrous layer, and CTF4-5 consists mostly of radially-migrating and sojourning younger neurons that have recently left the cerebellar NEP. On the basis of neurogenetic dating studies in the rat, we identify the first wave of cells in CTF2 as the early-generated deep nuclear neurons which form the nuclear transition zone or NTZ (Altman and Bayer, 1997). The human NTZ has three components, the presumed migrating and sojourning neurons of the future fastigial nucleus (NTZ1), interpositus nucleus (NTZ2), and the late-developing, and as yet small, dentate nucleus (NTZ3). The cerebellar NEP may begin to form as early as GW4.0 (Figure 20B) and it is clearly recognizable as a distinct entity by GW5.0 (Figure 21A). By GW5.5, the cerebellar NEP has two components, the vermal C1 and intermediate C2 posteriorly (Figure 38A, top), and an additional division, the lateral C3, anteriorly (Figure 38A, bottom). The cells of NTZ1 and NTZ2 that uniformly abut C1 and C2 posteriorly are presumed to be young neurons that have recently radially migrated a short distance from the NEP matrices. The presumably earlier generated neurons situated superficially in the NTZ of the anterior cerebellum appear to migrate tangentially toward the midline. In older embryos—GW6.5 (Figure 38B), GW7.0 (Figure 38C) and GW7.5 (Figure 38D)—the tangentially migrating cells of the NTZ (particularly those of NTZ1 in the anterior cerebellum) begin to form a growing superficial mass of cells, which we identify as the sojourning neurons of the fastigial nucleus. As the vermis fuses in the GW8.5 embryo (Figure 38E), the axons of these neurons cross the midline to form the hook bundle. As the cells of the cerebellar NTZ migrate tangentially, new waves of radially migrating cells (CFT4+5) appear to leave the cerebellar NEP in the GW 6.5 and GW7.0 embryos (Figure 38B, C). These may be straggling deep neurons and/or the earliest complement of Purkinje cells. The radial migration of the bulk of Purkinje cells appears to reach its peak in the GW7.5 embryo when they form a crescent-shaped mass of densely packed and darkly staining cells outside the NEP both in the posterior cerebellum (Figure 38D, top) and the anterior cerebellum (Figure 38D, bottom). The packing density of these cells decreases in the GW8.5 (Figure 38E) and GW9 (Figure 39A) specimens, suggesting that the Purkinje cells begin to disperse as they ascend toward
the surface. By GW11, the ascending Purkinje cells form a crescent-shaped mass superficially, and the dentate, interpositus and fastigial nuclei are now settling in the depth of the cerebellum (Figure 39B). We have suggested earlier that these elaborate migratory movements, and some others that we describe below, are part of a choreographed morphogenetic process responsible for the wiring of the complex circuitry of the maturing cerebellum (Altman and Bayer, 1997). The first step in this process, the upward migration of Purkinje cells, is associated with the spreading of a secondary germinal matrix, the external germinal layer, over the surface of the formative cerebellar cortex, as we describe below. Secondary Germinal Matrices. Proliferative NEP cells in some regions of the CNS generate not only differentiating neurons but also fate-restricted neurogenic precursor cells that retain their proliferative potency after they have left the ventricular shoreline. These secondary matrices include the subventricular zone (SVZ) of the neocortex and the basal ganglia, the subgranular zone (SGZ) of the hippocampal dentate gyrus, and the external germinal layers (EGL) of the cerebellar cortex and cochlear nuclei. We proposed some time ago (Altman and Das, 1965b) that these secondary germinal matrices share two properties. First, they generate microneurons, neurons that develop locally arborizing short axons that form the fine (local) circuitry of specific brain regions. This is in contrast to the primary NEP matrix that generates macroneurons, a variety of large neurons that sprout long axons that interconnect distant brain regions and form the gross (global) circuitry of the CNS. Second, the microneurons of a particular brain region are generated after its macroneurons have been produced. This occurs in some brain regions during the late gestational period, in other regions postnatally during infancy, and in a few of them through adulthood. For instance, the subpial EGL of the cerebellum, which spins off a component of the dorsal rhombic lip (the germinal trigone) and spreads over the surface of the cerebellum, begins to produce its microneurons (granule, basket, and stellate cells) after the cerebellar NEP has generated its macroneurons, the deep neurons and the Purkinje cells (Altman and Bayer, 1997). The EGL begins to form in the human cerebellum between GW7.5 and GW8.5 (Figure 38D, E) and by GW11 it forms a subpial canopy over the entire formative cerebellar cortex (Figure 39B). Significantly, the EGL that persists in rats until about postnatal day 21, the age they are weaned (Altman and Bayer, 1997), is still present in human cerebellum through the second year of postnatal life (Raaf and Kernohan, 1944; our unpublished observations). The descent of cerebellar granule cells into the formative cerebellar cortex to form the internal granular layer, leaving behind their axons, the parallel fibers, in the molecular layer, begins after the ascending Purkinje cells have commenced to sprout dendrites. The outcome of these choreographed movements of macroneurons and microneurons, such as the ascent of Text continues on page 481
473
A. E15 Rat
Posterior commissure
Pretectal NEP
ABBREVIATIONS:
mesencephalic superventricle
MESENCEPHALON
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP Tegmental EGL - External germinal layer NEP NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons) NTZ3 - Lateral (putative dentate neurons) isthmal canal
ISTHMUS
Isthmal NEP NTZ1
FUTURE VERMIS
FUTURE INTERMEDIATE HEMISPHERE
NTZ2 rhombencephalic superventricle
C1 Upper rhombic lip
Medial cerebellar notch
C2
Posterior commissure
Medullary velum
B. GW7 Human, M2155 Figure 36. The configuration of the anterior cerebellar NEP in rat (A) and human (B) at comparable stages of brain development. In the rat, the cerebellar NEP has two divisions, C1, the primordium of the vermis, and C2, the primordium of the phylogenetically older ("intermediate") hemisphere. In humans, it has three divisions with the added C3, the primordium of the neocerebellar lateral hemisphere. Coronal sections.
ANTERIOR CEREBELLUM
0.5 mm
Pretectal NEP
mesencephalic superventricle
Tegmental NEP
MESENCEPHALON
isthmal canal
ISTHMUS
Isthmal NEP NTZ1
FUTURE VERMIS
ANTERIOR CEREBELLUM FUTURE INTERMEDIATE HEMISPHERE
NTZ2
FUTURE LATERAL HEMISPHERE
NTZ3
C1 C2
Upper rhombic lip Medullary velum
C3
rhombencephalic superventricle
Medial cerebellar notch
Lateral cerebellar notch
0.5 mm
474 isthmal canal
GW6.5 Coronal, M2051, Anterior Cerebellum NTZ1
ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP CTF - Cerebellar transitional field NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons) NTZ3 - Lateral (putative dentate neurons)
Isthmal NEP NTZ2
Tangentially migrating deep neurons in the superficial NTZ (CTF2)
CTF1 CTF2 CTF3 CTF4+5
Medial cerebellar notch
C2
NTZ3
Future intermediate hemisphere
Future vermis rhombencephalic superventricle
Radially migrating deep neurons
C3 Upper rhombic lip
C1
Lateral cerebellar notch
Future lateral hemisphere
Figure 37. Three components of the human cerebellar NEP (C1, C2, C3), the presumed primordia of the vermis, intermediate hemisphere, and the lateral hemisphere, and the organization of the cerebellar transitional field in a GW6.5 embryo. CTF1 is a superficial fibrous layer; CTF2 consists mostly of tangentially migrating, earlier-generated (older) deep nuclear neurons (NTZ1, NTZ2, NTZ3; superficial arrows); and CTF4+5 consist mostly of radially migrating, later-generated (younger) neurons (double-headed arrows). Coronal section.
Figure 38A. GW5.5 Coronal, M2161 ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP GEP - Glioepithelium NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons) NTZ3 - Lateral (putative dentate neurons)
Inferior collicular NEP
Future vermis
Future intermediate hemisphere
NTZ1
C1
Isthmal NEP
C2
isthmal canal
Upper rhombic lip
Posterior cerebellum NTZ1
NTZ2
NTZ2
Future lateral hemisphere
Upper rhombic lip
Trochlear nerve (IV) decussation
Trochlear nerve GEP
Figure 38 (this page and the following four pages). Coronal sections of the developing posterior cerebellum (top) and anterior cerebellum (bottom) from embryos of the following ages: GW5.5 (A), GW6.5 (B), GW7.0 (C), GW7.5 (D), and GW8.5 (E). The vermal NEP (C1) develops earlier and is more prominent posteriorly; the hemispheric NEP (C3) develops more slowly and is prominent anteriorly. The tangentially migrating deep neurons (NTZ) accumulate superficially in the GW7.5 embryo and the axons of the putative fastigial nucleus neurons cross to the opposite side as the vermis fuses medially in the GW8.5 embryo. Concurrently, the radially migrating and sojourning Purkinje cells form a large crescent-shaped mass in the depth of the formative cerebellum. The subsequent ascent of Purkinje cells toward the surface is associated with the formation and spread of the EGL beneath the pia.
C2
Medial cerebellar notch
C1 rhombencephalic superventricle
Radially migrating deep neurons
Anterior cerebellum
C3
Tangentially migrating deep neurons NTZ3
Lateral cerebellar notch?
Medullary velum
475
476
Figure 38B. GW6.5 Coronal, M2051 ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP GEP - Glioepithelium NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons) NTZ3 - Lateral (putative dentate neurons)
Inferior collicular NEP
Posterior cerebellum
Future vermis
C1
NTZ1
Future intermediate hemisphere
Trochlear nerve (IV) decussation
Trochlear nerve GEP
isthmal canal
Tangentially migrating deep neurons
NTZ2
C2 Medial cerebellar notch
Upper rhombic lip
Radially migrating deep neurons
NTZ1
Tangentially migrating deep neurons
NTZ2
Future lateral hemisphere
Isthmal NEP
NTZ3
C2 Upper rhombic lip
C3 Lateral cerebellar notch
Medial cerebellar notch
C1
rhombencephalic superventricle
Anterior cerebellum
Figure 38C. GW7 Coronal, M2246
Inferior collicular NEP
ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP GEP - Glioepithelium NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons) NTZ3 - Lateral (putative dentate neurons)
Trochlear nerve (IV) decussation Trochlear nerve GEP
Future vermis
C1
NTZ1
Future intermediate hemisphere
Posterior cerebellum Tangentially migrating deep neurons
NTZ2
Radially migrating deep neurons and earliest Purkinje cells
C2
isthmal canal
Upper rhombic lip
NTZ1
NTZ1
Isthmal NEP
NTZ2
Future lateral hemisphere
Upper rhombic lip
NTZ3
Medial cerebellar notch
C2
Anterior cerebellum
C1 rhombencephalic superventricle
C3
Lateral cerebellar notch
477
478
Figure 38D. GW7.5 Coronal, M2248 ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP EGL - External germinal layer NTZ - Nuclear transitional zone NTZ1 - Medial (putative fastigial neurons) NTZ2 - Intermediate (putative interpositus neurons)
Inferior colliculus
Future vermis
Tangentially migrating deep neurons
NTZ1
Posterior cerebellum
Upper rhombic lip
NTZ2
Radially migrating Purkinje cells
C1
Future intermediate hemisphere
isthmal canal
Sojourning Purkinje cells
C2 Pioneer EGL Budding germinal trigone
Isthmal NEP
Dentate and interpositus nuclei in superficial position
PONS
NTZ3
Future intermediate and lateral hemisphere
Anterior cerebellum
Medial cerebellar notch
C2/3
C2
Pontine NEP
rhombencephalic superventricle
Figure 38E. GW8.5 Coronal, M2050
Inferior collicular NEP
ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP EGL - External germinal layer
Posterior cerebellum
Vermal fusion field
Inferior colliculus
Future vermis and intermediate hemisphere
Transversely oriented fastigial neurons sprouting decussating fibers of the hook bundle (before descent)
Spreading EGL
Tangentially migrating Purkinje cells (beneath EGL) Germinal trigone (upper rhombic lip)
Sojourning Purkinje cells
C1/2
Radially migrating Purkinje cells
C2 Spreading EGL Tangentially migrating Purkinje cells (beneath EGL) Germinal trigone (upper rhombic lip)
Anterior cerebellum
Future intermediate and lateral hemisphere
Rhombencephalic choroid plexus
PONS
Dentate and interpositus nuclei in superficial position
Pontine NEP
Medial cerebellar notch
C2/3 rhombencephalic superventricle
479
480
A. GW9 Coronal, M841
Future site of vermal fusion
Future EGL trajectory
ABBREVIATIONS:
NEP - Neuroepithelium C1 - Medial cerebellar NEP C2 - Intermediate cerebellar NEP C3 - Lateral cerebellar NEP EGL - External germinal layer G/EP - Glioepithelium/ependyma
Medially spreading EGL
Dentate and interpositus nuclei in superficial position
Inferior cerebellar peduncle
fusing isthmal canal
Ascending Purkinje cells approaching EGL
rhombencephalic superventricle
C2+C3 Germinal trigone (upper rhombic lip)
Sojourning and ascending Purkinje cells
B. GW11 Coronal, Y1-59 LATERAL HEMISPHERE
l je ce rkin n u f P tio s o o si as ial p m ic rf
in
ge n Late r
INTERMEDIATE HEMISPHERE
ls
er a te su d pe
EGL
Descended deep nucl ei Interpositus nucleus
Dentate nucleus
VERMIS
Fastigial nucleus
Earlier generated dispersing Purkinje cells
Fusion site of vermal NEP (C1)
Cerebellar G/EP
Germinal trigone (upper rhombic lip)
Rhombencephalic choroid plexus
rhombencephalic superventricle
Figure 39. A. The ascent of Purkinje cells toward the surface in a GW9 embryo as, concurrently, the EGL begins to spread medially. B. The Purkinje cells are settling superficially beneath the canopy of EGL cells in this GW11 fetus, and the fastigial, interpositus, and dentate nuclei are assuming their final position in the depth of the vermis, and the intermediate and lateral hemispheres. Coronal sections.
481 Purkinje cells through the field of deep neurons, and the descent of granule cells through the Purkinje cell layer is that, by leaving behind their trailing axons, the stereotypic input-output circuitry of the cerebellum is established (Altman and Bayer, 1997). The pattern of neurogenesis and migration of hippocampal macroneurons and microneurons is quite different than that of the cerebellum. As it was demonstrated in the rat, hippocampal macroneurons (the pyramidal cells of Ammon’s horn) are produced early during fetal development (Bayer, 1980a, b). The dentate NEP produces an early set of perinatal microneurons (granule cells), while another set of progenitor cells forms the secondary germinal matrix of the subgranular zone (SGZ), which persists through adulthood (e.g., Altman and Bayer, 1975; Kempermann, 2006). It is now known, that the production of hippocampal granule cells through adulthood is not limited to lower mammals but is also a significant phenomenon in primates (e.g., Gould et al., 1999). In the human telencephalon, the hippocampal dentate NEP is present by GW9; but the dentate gyrus is not recognizable as a distinct entity until the second trimester (Volume 3 of this Atlas: Bayer and Altman, 2005). The time course of secondary matrix neurogenesis is again different in the cerebral cortex, a site where, according to experimental evidence in rodents, early- and late-generated neurons settle in an “inside-out” pattern in the gray matter (Angevine and Sidman, 1961). The lateral ventricles that are lined by NEP cells shrink considerably during the third trimester but, where present, an appreciable NEP/SVZ matrix is still present at the time of birth (Volume 2 of this Atlas: Bayer and Altman, 2004a). The SVZ that persists anteriorly through adulthood in animals has been shown to be a source of neurons that, migrating by way of the rostral migratory stream, supply neurons to the olfactory bulb not only in the rat (Altman, 1969) but also in monkeys (e.g., Pencea et al., 2001) and humans (Bedard and Parent, 2004). According to our interpretation of the experimental data obtained in rats, the early-generated layer VI and layer V cortical output neurons are progeny of the cortical NEP, and the later-generated granule cells that settle in the granular layer (IV) and other locally arborizing neurons that settle in the supragranular layers (III-II) are progeny of both the NEP and SVZ (Bayer and Altman, 1991a). Others have argued that the SVZ of the basal ganglia is the source of cortical interneurons (e.g., Anderson et al., 2002). It has been reported that the transcription factor Tlx is necessary for the full formation of the supragranular layers (Land and Monaghan, 2003). In the material available to us, we could not accurately date the emergence of the cortical SVZ because of the difficulty of distinguishing it from the NEP. However, as Kershman (1938) illustrated some time ago, the SVZ is prominent in the GW11 cerebral cortex (Figure 40). The basal ganglionic SVZ may begin to form as early as GW7.5-GW8 (Figure 16H, I), and both the cortical and the striatal SVZ persist as prominent ger-
Layer I
Cortical Plate
Stratified transitional field
Cortical SVZ
Cortical NEP
Figure 40. Kershman’s (1938) illustration of the developing cerebral cortex in a GW11 human fetus, showing the cytological difference between the neuroepithelium (NEP) adjacent to the ventricle and the subventricular zone (SVZ). The spindle-shaped (pseudostratified) NEP cells are oriented at a right angle to the ventricular lining and they undergo mitotic division near the lumen. The variably shaped SVZ cells undergo mitosis within this secondary germinal matrix. Labeling modified.
minal zones in newborns (Volume 2: Bayer and Altman, 2004a). The formation of the internal capsule as early as GW8 (Figure 31B) may initially contain only thalamocortical fibers. The outflow of corticofugal efferents and the formation of the cerebral peduncle between GW10 and GW13.5 (Figure 33A, B) suggests that the cortical output
482 neurons are probably generated before the cortical SVZ is forming or becomes prominent. Indeed, the cortical plate that forms between GW8.0 and GW8.5 (Figure 32C, D) may contain the earliest layer VI corticofugal neurons generated by the primary NEP and the generation of layer V neurons may follow soon thereafter. Gliogenesis and Fate-Restricted Glioepithelia. Within a given brain region, neurogenesis and gliogenesis are generally sequential processes, and the generation of certain types of neuroglia, like astrocytes, antedates the production of oligodendrocytes that myelinate axons. As we have documented in the rat with 3H-thymidine autoradiography, there are many CNS sites where germinal matrices with proliferating cells persist for some time after the cessation of neurogenesis (e.g., Bayer and Altman, 1991). We called these transformed germinal matrices glioepithelia (GEPs). These proliferating cells leave the GEP, become dispersed through the parenchyma, and generate fate-restricted neuroglial precursors that multiply through adulthood (Altman, 1966). We have also found that at sites where the enduring ventricle will be lined with specialized ependymal cells, the administration of 3H-thymidine at a late phase of fetal or early prenatal development tags ependymal cells that remain labeled in adults; we call these germinal sites glioepithelial/ependymal matrices (G/EPs). Finally, cytological observations in the human CNS, in particular in myelin-stained sections of the spinal cord, have established that myelination gliosis (the high rate of glial cell proliferation preceding the myelination of particular fiber tracts) is a late developmental phenomenon (Altman and Bayer, 2001; Volume 1 of this Atlas: Bayer and Altman, 2002). Lineage studies have confirmed that NEP cells can generate both neurons and glia, although it remains unclear whether it is the same line of proliferative cells that first gives rise to neurons and then to neuroglia or that there are two separate lines that are sequentially activated by external signals (Luskin et al., 1988, 1993; Walsh and Cepko, 1992; Williams and Price, 1995). The report that cultured cortical progenitor cells generate neurons when plated with cortical tissue from young embryos but produce neuroglia when plated with cortical tissue from adults (Morrow et al., 2001) supports the idea that extracellular influences can modify NEP cell fate. The gene, Brg1, has been implicated in the switch from neurogenic to gliogenic cell production, and proteins, such as Sox1 and Pax1, implicated in the maintenance of neurogenic potential are drastically reduced in Brg1 mutant mice (Matsumoto et al., 2006). In addition to the NEP-derived, late-generated glial progenitors, there are specialized germinal matrices that from the outset of CNS development are destined to produce only neuroglia. Prominent among these are perifascicular GEP matrices associated with early forming large fiber tracts, such as the fornical GEP. Moreover, we can also distinguish at the latter site a germinal matrix that generates the specialized cells of the choroid plexus (Altman and
Bayer, 1990a). Finally, we present suggestive evidence that, as in the rat brain (Van Hartesveldt et al., 1986), so also in the human CNS, there are specialized types of glia present at certain sites, we call them morphocytes, that play a formative role in the structural transformations of the developing CNS. For instance, in the midline of the spinal cord, morphocytes of the roof plate and the floor plate are responsible for the development of the H-shape configuration of the gray matter (Altman and Bayer, 2001), and in the hindbrain morphocytes seem to act as guy wires to produce and maintain the structural stability of the medullary, pontine, mesencephalic, and diencephalic flexures (Volume 4 of the Atlas and the present volume). Nestin expression has been associated with the midline raphe glial structure in the early human fetus (Takano and Becker, 1997).
H. Centro-Central Signaling and the Morphogenetic Maturation of the CNS Centro-Central Induction and Signaling. From the perspective of its input-output organization, the vertebrate CNS has two principal components: (i) first-order structures that are in direct contact with peripheral sense organs, skeletal muscles, smooth muscles, and glands; and (ii) higher-order structures that are directly (synaptically) connected with one another but only indirectly (by way of the first-order structures) with the periphery. Examples of first-order sensory CNS structures are the dorsal horn in the spinal cord, which receives input from the trunk, limb, and neck sensors by way of spinal afferents; the trigeminal nuclei that receive sensory input from the face and mouth by way of trigeminal afferents; and the olfactory bulb that receives direct peripheral input from the olfactory epithelium. Examples of first-order CNS effector structures are the motor nuclei of the ventral horn and the cranial motor nuclei that directly innervate skeletal muscles, and the secretory neurons of the hypothalamus and preoptic area that produce releasing factors that, conveyed to the pituitary gland, control the visceral system. In contrast, the bulk of second- and higher-order CNS structures that relay and process sensory information and issue motor commands have no direct access to the periphery. Examples of intercalated somatosensory structures are the dorsal column nuclei in the medulla, the relay nuclei of the thalamus, the postcentral projection area in the cerebral cortex, and several cortical association areas involved in higher-order somatosensory information processing. From the perspective of morphogenetic regulation, the coordinated development of first-order CNS structures requires, as described earlier, reciprocal periphero-central induction and signaling, whereas the coordinated development of higher-order CNS structures requires centro-central signaling between components of a system that become interconnected during development. It is reasonable to assume that the induction and signaling mechanisms responsible for synchronizing the development of PNS and CNS structures, and those
483 responsible for interconnecting CNS structures with one another are different. The higher-order components of the CNS are interconnected with one another by way of long-distance nerve trunks, regional neural networks, and local circuits. The establishment of modality-specific and topographically organized projection systems—such as the selective and reciprocal interconnections between subdivisions of a particular sensory relay nucleus of the thalamus with a particular area of the neocortex—is dependent on the guided pathfinding of the growing axons of projection neurons that have to navigate over long distances to find their exact target. This requires centro-central signaling between source and target structures, as well as guideposts or beacons along a tortuous path. The regional ramification of the axons of interneurons, the spread and geometric configuration of their dendritic arbors, etc. must likewise be coordinated by reciprocal centro-central signaling among neighboring structures. It may be expected that the signaling mechanisms responsible for long-distance central interconnections, which establish the gross circuitry of the CNS, and the signaling mechanisms responsible for short-distance interconnections, which produce the fine circuitry of a local brain region, are also different. Centrocentral signaling between interconnected brain structures may involve parallel (synchronous) development, serial (hierarchical) development, or a combination of both. For example, the early development of lower-level components of the system (input-output structures) may trigger the later development of its higher level components (processing structures). In the human CNS, at least some of the long-range sensory connections are established by the late first trimester, and to some extent concurrently, at different levels within a system. An example is the early maturation of the medial lemniscal system in the somatosensory pathway and the relatively early maturation of the ventral thalamic nuclear complex (Volume 4 of this Atlas: Bayer and Altman, 2006). However, the establishment of the fine circuitry of CNS structures, through the interdigitation of macroneurons and microneurons, is a lengthy process that extends beyond the second and third trimesters and continues through the prenatal period of brain development. Relatively little is known about the mechanisms of centrocentral signaling except for axonal pathfinding. The Guidance of Axonal Pathfinding. The growing axons of the medial lemniscus exemplify pathfinding to a distant target. Originating in the dorsal column nuclei, these axons cross to the opposite side in the medulla (the arcuate decussation) and, bypassing various intermediate structures in the pons, isthmus, and the midbrain tegmentum, terminate in the somatosensory thalamus. Another example is the corticospinal tract whose axons, originating in the cerebral cortex, penetrate the corona radiata, move through the striatum, join the internal capsule, pass through the cerebral peduncle of the midbrain, penetrate and move
through the pontine gray and, upon reaching the medulla, most of them cross to the opposite side and descend in the spinal cord. We have described earlier the developmental timetable of the latter process in the human CNS (Altman and Bayer, 2001). Modern research indicates that the directed growth of pioneer axons toward distant targets depends on molecular guidance agents along their route, cues that are detected by receptor elements within the axon’s growth cones (Tessier-Lavigne and Goodman, 1996). These cues, acting as chemorepellants or chemoattractants, may adhere to or emanate from specific brain structures along the axon’s path, and in that way, the growing axon can use a trial-and-error method to locate its target. Specifically, the growth cone tips that encounter repellants withdraw or collapse, and those that encounter attractants expand. Among recognized repellant cues are the semaphorins that, interacting with the growth cone receptors (plexins and neuropilins) of advancing axons, cause the depolymerization of microtubules and F-actin in the growth cones that leads to their collapse (Fan et al., 1993; He et al., 1997; Fujisawa and Kitsukawa, 1998; Pasterkamp and Kolodkin, 2003). Netrin-1 (Métin et al., 1997; Richards et al., 1997; Finger et al., 2002) and semaphorins (Polleux et al., 1998) are among the putative chemoattractants implicated in the directed growth of corticofugal axons. Netrin-1 may also be involved in the guided growth of thalamocortical fibers (Braistead et al., 2000) and in the normal development of the circuitry of the hippocampus (Barralobre et al., 2000). In some brain regions, netrin-1 signaling is required for commissural fibers to cross to the opposite side (Serafini et al., 1996); in the medulla, netrin-1 is secreted by the floor plate and its absence in homozygous mutant mice results in the failure of medial lemniscal fibers to cross to the opposite side and turn to ascend rostrally (Kubota et al., 2004). Still another example of directed, long-distance axonal pathfinding is the guidance of the pioneering fibers of the ascending thalamocortical afferents. The internal capsule that contains the bulk of the thalamocortical fibers, is still absent in the developing human brain on GW7.5 (Figure 31F), and the cortical plate has yet to form. By GW8 thalamocortical fibers enter the expanding internal capsule (Figure 31G), which establishes a bridge between the diencephalon and the cortex, and a thin cortical plate begins to form dorsolaterally. By GW10, there is a massive outflow of afferents from the thalamus through the expanded internal capsule and, in addition to the thickening cortical plate, the different layers of the STF are beginning to form (Figure 33A). By GW11, we can track the different trajectories of thalamocortical fibers to some areas of the cerebral cortex; in particular, the visual radiation from the lateral geniculate nucleus, which makes a 180° turn (Meyer’s loop) around the caudate nucleus, proceeds caudally, and terminates in the occipital lobe (Volume 4 of this Atlas: Bayer and Altman, 2006). According to one hypothesis there are intrinsic regional differences in the proliferative
484 matrix of the cerebral cortex that will become the target of different afferent fibers and these regional differences are the foundation of areal specification (Rakic, 1988). We have demonstrated anterior-to-posterior (longitudinal) and lateral-to-dorsomedial (transverse) neurogenetic gradients in the rat cerebral cortex (Bayer and Altman, 1991), and suggested that these NEP maturation gradients may control not only the modality-specific selectivity of thalamocortical innervation but also the lateral-to-medial order in the ingrowth of thalamic afferents, as demonstrated in the mouse (Caviness and Frost, 1980). One set of studies has implicated Tbr1, Gbx2, and Pax6 in the initial outgrowth of thalamic fibers to the cortex and in the guidance of their long-range trajectory (Hevner et al., 2002; Molnár et al., 2003). Another series of investigations implicates Emx1, Emx2, Pax6, Gsh2, COUP-TFI, and Fgf8, which are expressed in dissimilar dorsal-to-ventral and anterior-toposterior gradients in the developing cerebral cortex (Gulisano et al., 1996; Liu et al., 2000; Stoykova et al., 2000; Yun et al., 2001; Torreson et al., 2000; Muzio et al., 2002; Bishop et al., 2003; Garel et al., 2003). These studies have not yet taken into consideration our evidence that rather than proceeding directly to the cortical plate, the sojourning cells of the STF are an intermediary target of thalamocortical afferents, and that there are pronounced regional differences in STF lamination patterns (Altman and Bayer, 2002; Volume 3 of this Atlas: Bayer and Altman, 2005). Once thalamocortical modality-specific projection has been established, the formation of topographic maps and the termination of arborizing axons in layer IV are probably controlled by different signaling agents than those guiding the initial growth of thalamic afferents. Among these signaling molecules are reelin secreted by the early generated Cajal-Retzius cells of the primordial plexiform layer, already discussed in the context of cell migration, and ephrins and their receptors (Castellani et al., 1998; Vanderhaeghen et al., 2000; Dufour et al., 2003; Bolz et al., 2004). One experiment compared the growth of thalamic axons toward cultured membranes from cortical layer IV to that of membranes from cortical layer V, a stratum that the thalamocortical fibers bypass on their way to layer IV. The thalamic axons exhibited arrested growth and increased branching density on their appropriate target tissues but interference with ephrin expression abolished this preferential termination pattern (Mann et al., 2002). Still other studies implicated N-cadherin (Huntley and Benson, 1999; Poskanzer et al., 2003) and Slit2 (Ozdinler and Erzurumlu, 2002) in the laminar termination of thalamocortical fibers in the cortex. N-cadherin (Riehl et al, 1997) and ephrins also appear to serve as guidance cues in the growth of retinal fibers (Birgbauer et al., 2001). According to a recent study (Lambot et al., 2005), there are differences in the gradients of ephrin expression in the developing visual system of animals with lateral eyes, in which most (or all) retinal axons cross to the opposite side in the optic chiasma, with ephrin expression in the developing visual
system of humans with medial eyes, where only the nasal half of the retina projects contralaterally but the temporal half projects ipsilaterally.
I. Summary: The Epochs, Phases, and Mechanisms of CNS Development The reviewed descriptive and experimental evidence suggests that the prenatal development of the CNS consists of successive epochs, each with multiple phases, that are guided by different morphogenetic mechanisms. The first epoch (Figure 41) consists of several phases. The initial phase, which is not dealt with in this Atlas, is the formation of the neural plate, containing pluripotent progenitor cells that give rise to the neural elements of the CNS and PNS as well as some non-neural tissue and organs. The next phase is the fusion of the central component of the neural plate, which results in the formation of the neural tube (the future spinal cord) along the trunk caudally, and the cephalic vesicles (the future brain) in the head region rostrally (Figure 22). This is followed by the proliferation of stockbuilding NEP cells in association with the earliest specification of their future diversity through reciprocal periphero-central transactions with the primordial components of the developing body, including the neural crest, somites, and notochord caudally, and the preplacodes rostrally. That early diversification becomes manifest in the future spinal cord as the tubular NEP is partitioned into sensory and motor compartments. This occurs under the peripheral inductive and signaling influence of the neural crest and somites, on the one hand, and the notochord, on the other. The diversification of the stockbuilding NEP cells in the different divisions of the future brain is under a different set of peripheral influences. Rostrally, the stockbuilding prosencephalic NEP expands greatly in association with the ballooning of the prosencephalic superventricle, and it is under the reciprocal influence of the cephalic (olfactory, optic, and pituitary) preplacodes. Caudally, the diversifying rhombomere NEPs, which grow in association with the expansion of the rhombencephalic superventricle, interact with the branchial (orofacial, octaval, and visceral) preplacodes, and arches I, II, III, and IV with which they are associated. The second epoch of CNS development, likewise, consists of several phases, and these phases differ caudally in the developing spinal cord and rostrally in the developing brain (Figure 42). In the developing spinal cord, several periphero-central morphogenetic events take place concurrently. (i) The skin senses of the trunk, limbs, and neck, and (ii) the bipolar neurons of the spinal dorsal root ganglia differentiate peripherally. The latter (iii) interconnect the sense organs with the sensory-relay neurons in the dorsal horn and dorsal column nuclei centrally. At about the same time, (iv) the various peripheral muscles of the trunk, limb and neck conjointly differentiate with (v) the motor neurons that innervate them, which form distinct columns in
485 the ventral horn centrally. In the developing brain, the different components of the ventral telencephalon and diencephalon (forebrain) interact with the diversifying cephalic placodes, and different components of the rhombencephalon (hindbrain) do the same with the diversifying branchial placodes. In the developing forebrain, aided by reciprocal periphero-central induction and signaling, (i) the neurons in the olfactory epithelium, the progeny of the olfactory placode, differentiate conjointly with the neurons in the olfactory bulb. (ii) The cells in the crystalline lens of the eye, derived from the lens placode, differentiate conjointly with the neurons in the retina and cells in the pigment epithelium. (iii) The secretory cells in the adenohypophysis, derived from the pituitary placode, differentiate conjointly with the neurosecretory cells in the hypothalamus and pituicytes in the neurohypophysis. In the developing hindbrain, (iv) the peripheral neurons in the orofacial (trigeminal and facial) ganglia, derived from branchial placodes, conjointly differentiate with central neurons derived from R2 and R3. (v) The peripheral neurons in the vestibulocochlear ganglion, derived from the otic vesicle, conjointly differentiate with the central neurons derived from R4 and R5. (vi) The glossopharyngeal and vagal ganglia, derived from branchial placodes, conjointly differentiate with the central glossopharyngeal and vagal neurons derived from R6 and R7. In sharp contrast to these forebrain and hindbrain regions that have direct peripheral connections, many brain regions are devoid of surrounding placodes such as the cerebral cortex, basal ganglia, thalamus, tectum, and cerebellum. In the absence of direct contact with the developing peripheral sense organs, muscles, and other effectors, the coordinated development of these brain structures is dependent on endogenous mechanisms and centro-central induction and signaling. One facet of this process, as we described earlier, is the directed growth of axons that interconnect different brain structures and produce the brain’s gross and fine circuitry. Another is the migratory movement of young neurons that contact one another in passing and leave behind trailing axons, much like a spider building its web. This phenomenon is exemplified by the choreographed movements of sequentially generated cerebellar neurons, as deduced from experimental studies in the rat. The first phase of cerebellar development is the formation and expansion of the stockbuilding cerebellar NEP (Figure 43A). The second phase is the radial migration of the earliest set of differentiating neurons, the future deep nuclei, which form the first parenchymal cell layer abutting the NEP (Figure 43B). The third phase is the exodus of a new set of differentiating neurons from the cerebellar NEP, the Purkinje cells, which displace the layer of deep neurons outward (Figure 43C). The fourth phase is the tangential migration of deep neurons over the cerebellar surface (Figure 43D), a process coupled with the sprouting of axons that cross to the opposite side in the vermis. During the fifth phase, deep neurons and Purkinje cells exchange
places. Deep neurons migrate downward, while Purkinje cells migrate upward (Figure 43E). That establishes the mature pattern (Figure 43F) where the Purkinje neurons form a superficial cortical layer and the deep nuclear neurons settle in the core of the cerebellum. This important event occurs conjointly with the formation of a new neurogenic proliferative matrix, the EGL, which spreads superficially to form a subpial canopy over the expanding cerebellum (Figure 43E, F). Perhaps due to some dual attractant/ repellant force exerted by the EGL, the sojourning Purkinje cells ascend to the surface and the deep neurons descend. We hypothesized earlier (Altman and Bayer, 1997) that cohorts of deep neurons and Purkinje cells make enduring contacts with each other while they become intermingled for a period and then pass each other. The deep neurons, which already have extracerebellar inputs and are sprouting cerebellofugal efferents, descend together with the trailing axons of Purkinje cells attached. The ascending Purkinje cells carry with them branches of some extracerebellar afferents (climbing fibers) that also contact the deep neurons. As the superficially situated masses of Purkinje cells disperse beneath the canopy of the EGL to form a monolayer (Figure 43G), the subsequent phases of cerebellar development begin to unfold leading to formation of the fine circuitry of the cerebellar cortex. One facet of this is the descending migration of granule cells from the EGL, through the molecular and Purkinje cell layers, and into the granular layer (arrows, Figure 43G). The descending granule cells leave their axons (the parallel fibers) behind in the molecular layer and establish contacts with growing Purkinje cell dendrites. Granule cell dendrites sprout in the granular layer to establish contact with the specialized endings of mossy fiber afferents. The major function of the elaborate choreographed movements of different cerebellar neurons, in conjunction with the directed growth of their axons and dendrites, is to produce the stereotyped complex circuitry of the cerebellar cortex.
J. A Note on the Functional Maturation of the Human CNS The Functional Maturation of the CNS. The function of the CNS is to gather information about prevailing conditions and salient events in the external world in relation to the changing conditions and needs of the body interior, process and integrate that information, and initiate appropriate behavioral and physiological actions and reactions to them. Neither the proliferative progenitors of neurons nor the migrating and sojourning young neurons lacking axons and dendrites can mediate these functions. It is only after the settled neurons have begun to receive afferent input and establish synaptic connections with one another, and the fibers of motor neurons contact muscles, that the CNS can commence to perform its complex regulatory functions. The maturation of these functional CNS networks and circuits is a protracted process that commences during the early fetal period and continues through the late-fetal, neoText continues on page 489
486
RHOM
BENCEPHA
Cerebellar NEP
N
LON
Medullary velum
rhombencephalic superventricle
SOMITIC/NEURAL CREST DOMAINS (Dorsal)
Precerebellar NEP
R h o m b e s R2 R3 R4 o m e r R7 R5 R6
central canal
PR ( O C E P H A L I C tic) lf a c BRANCHIAL (Op tory) PREPLACODES
Arch II
Arch I (Orofacial)
NOTOCHORDAL DOMAINS (Ventral)
Arch IV Arch III (Visceral) OTIC VESICLE (Octaval)
P L A C O D A L
DORSAL NEP VENTRAL NEP
E
PL (H A C O yp oph D E S y s e a l)
O
P
N
mesencephalic superventricle
pr su ose pe nc rv ep en ha t r l ic ic l e
PR
OSENCEPH
A
L
PRIMORDIAL NEPs
SE
E NC
LO HA
M
E
SPINAL CORD
D O M A I N S
Figure 41. The first epoch of CNS development. Schematic illustration of the reciprocal periphero-central signaling potential between components of the peripheral cephalic preplacodes (red) and the ventral telencephalic NEP (pink); between components of the peripheral branchial placodes (dark green) and the rhombomeric NEP compartments (light green); and between the peripheral somites and notochord (orange) and the dorsal and ventral spinal NEPs (blue).
CENTRO-CENTRAL INDUCTION FIELD
T
d supience erv pha ent lic ric le Hypotha lamus
t su elen pe ce rv ph en al tr ic icl e
um
Olfactory epithelium
Dorsal root ganglia and dorsal roots of spinal nerves
Medullary velum
rhombencephalic superventricle Pon
s
R2 R3 R4
Nerve I (olfactory) Pigment epithelium
SKIN SENSES
rebel l Ce
s
Nerve II (optic)
m su es pe en rv ce en ph t a me ri li Teg nt cle c
mu Isth
Olfactory bulb
SPINAL CORD
m
a
T e c t
um
al gang li Bas
a
C e r e b r
us am us l ha lam ha
u
T
r t e x
l
c
o
l l a M e d u
R5
R6
central canal
R7
DORSAL HORN VENTRAL HORN
Lens Retina
Eye
Adenohypophysis Neurohypophysis
Pituitary gland
Trigeminal ganglion and nerve V
Facial ganglion and nerve VII
CEPHALIC
PREPLACODAL DERIVATIVES
Ventral roots of spinal nerves
OTIC VESICLE
Vestibulocochlear ganglion and nerve VIII
BRANCHIAL
MUSCLES Vagal Glossopharyngeal ganglia and ganglia and nerve X nerve IX
NEURAL CREST/ SOMITIC DERIVATIVES
PERIPHERO-CENTRAL INDUCTION FIELD Figure 42. Second epoch of CNS development. Schematic illustration of the reciprocal periphero-central signaling potential between the olfactory epithelium, the lens of the eye, and the adenohypophysis, derived from the cephalic placodes (red), with the olfactory bulb, the retina, and the neurohypophysis, respectively, derived from the ventral telencephalic NEP (pink); between the cranial ganglia and otic vesicle derived from the branchial placodes (dark green) and the differentiating neurons of the rhombomeric NEPs (light green); and the differentiating spinal ganglia and muscles (orange) and the differentiating neurons of the dorsal horn and ventral horn derived from the spinal NEP (blue).
487
488
A
Connection to isthmus and inferior colliculus
Trochlear nucleus Primary cerebellar NEP
Purkinje cell layer
G
Upper rhombic lip
B
Neurogenic EGL produces descending granule cells
Granule cell layer
Deep neurons Radially migrating deep neurons
C
Tangentially migrating deep neurons Sojourning Purkinje cells
Germinal trigone remains large
Radially migrating Purkinje cells Radially migrating (short arrows) deep neurons (long arrows)
D
Tangentially migrating deep neurons
F
Stockbuilding EGL covers the entire cortical surface
Choroid plexus continues to expand
Ascending Purkinje cells disperse and sort into discrete clumps
Dispersing EGL
Radially migrating Purkinje cells
E
Deep neurons accumulate in specific nuclei
Ascending Purkinje cells
Germinal trigone
Descending deep neurons Choroid plexus
Figure 43. Third epoch of CNS development (centro-central induction) as illustrated by the several stages of cerebellar development. Light green, primary cerebellar neuroepithelium (NEP); yellow, deep neurons; red, Purkinje cells; dark green, external germinal layer (EGL); blue, granule cell layer; brown, choroid plexus Arrows indicate cell migrations. See text on page 485 for more details.
489 natal, and juvenile periods, and may not end until late adulthood. Importantly, there are pronounced differences in the maturation of different components of the CNS in relation to the specific functions they mediate and in terms of their position in the serial and hierarchic organization of those functions. For instance, in the maturating human spinal cord, motor fibers begin to exit the ventral horn as early as GW5.0. Sensory fibers of the spinal ganglia begin to penetrate the dorsal horn by GW5.5 (Altman and Bayer, 2001; Volume 1 of this Atlas: Bayer and Altman, 2002). In the maturing brain, somatosensory neurons of the trigeminal ganglion line up outside the trigeminal NEP (R2) as early as GW5.5 (Figure 27B), and its fibers penetrate it by GW6.5 (Figure 29A). This, of course, does not mean that these afferents and efferents are functional in the sense that they convey sensory messages and trigger motor commands. There is considerable scientific and public interest in the prenatal development of the human brain in relation to the mental status of the embryo and fetus. Studies in the first half of the 20th century with aborted fetuses have indicated that embryos of about 20 to 21 mm CR length (corresponding to the GW7.5 specimens illustrated in Volume 4 of this Atlas: Bayer and Altman, 2006) begin to reliably respond to tactile stimulation with holokinetic (“total pattern”) body movements (Fitzgerald and Windle, 1942; Hooker, 1942). In GW10 fetuses (CR 48.5 mm) ideokinetic or isolated movements were also elicited, such as partial closure of the fingers (though not effective grasping) when the palm of the hand is stimulated (Humphrey, 1964). The more recent introduction of ultrasonic recording techniques has permitted the observation of the emergence of “spontaneous” fetal behavior in normal embryos and fetuses in utero. A pioneering study (de Vries, 1982, 1985) showed that the holokinetic “startle” response emerges as early as GW6, and isolated arm and leg movements emerge by GW7. These embryos would represent some of the oldest specimens presented in this volume. According to a more recent study with improved ultrasonic recording methods (Kurjak et al., 2005), isolated arm and leg movements increase in frequency during the late first trimester but head turning, and the hand contacting the head, do not occur with high frequency until the second trimester. Are the late-embryonic and early-fetal movements reflex reactions mediated by lower-level spinal cord and brain stem mechanisms, or are they budding voluntary activities carried out under higher-level cortical guidance, by mental processes, such as feelings and emotions, perception and volition? We have raised these questions earlier in the context of our study of the development of the sensorimo-
tor circuitry of the human spinal cord (Altman and Bayer, 2001). The substrate of the sensorimotor reflex arc in the spinal cord begins to form between GW7 and GW8 because the collateral branches of dorsal root afferents reach the ventral horn motor neurons during this period. Since the earliest corticospinal tract fibers do not reach the spinal cord until about GW19, we proposed that the isolated limb movements displayed by embryos of that age must be reflex reactions rather than voluntary activities. We can expand on this inference on the basis of the morphogenetic evidence presented in Volume 4 of this Atlas (Bayer and Altman, 2006) and in the present volume by stating that it is most unlikely that first-trimester embryos can experience cortically mediated mental processes. Cortically mediated sentient responses to somatosensory stimulation, which could be the source of internally generated sensations or perceptions in utero, presumes the operation of the following hierarchically arranged neural mechanisms: conduction of nerve impulses through the dorsal funiculus and through a chain of relay neurons and afferents in the dorsal column nuclei of the medulla and the medial lemniscus; synaptic maturation of the somatosensory relay nuclei of the thalamus, the site where the thalamocortical fibers terminate and afferents of the somatosensory cortex originate; and finally, the settling of late-generated cortical neurons in the cortical plate and their synaptic maturation in the cortical gray matter. While the relay neurons of the dorsal column nuclei and some of the thalamic neurons are generated during the early first trimester (we have no information when synapses are beginning to form here), the internal capsule that contains the ascending thalamocortical fibers to the cortex does not begin to form until GW8. It is at this age that, passing through the internal capsule, the earliest somatosensory fibers approach the base of the formative cerebral cortex. These fibers begin to penetrate the sojourn zone of the stratified transitional field by GW9 and that process continues through GW11. It is probable (but this needs to be experimentally verified) that the neurons of layer IV of the cortex, the principal target of thalamocortical fibers, are still in the stratified transitional field during that period and that synaptic connections in the formative gray matter, the cortical plate, are yet to develop. If this is correct, there is no functional connection between the thalamus and cells of the cortical plate during the first trimester of embryonic and fetal development and, therefore, the neural substrate for cortically mediated sentient responses to somatosensory stimuli is still missing during this period. It is possible, but this needs to be investigated morphologically and physiologically, that the neural mechanisms of rudimentary sentience begin to mature slowly some time during the second trimester.
490
APPENDIX APPENDIX
Timespans Timespansof ofNeurogenesis Neurogenesis A neuron is born when a proliferating neurogenic precursor cell gives rise to a postmitotic cell that displays cytological features or expresses molecular markers of a young neuron. While many current studies rely on molecular markers as the criterion of neurogenesis, we have used 3 H-thymidine autoradiography to determine the cessation of mitotic division and the birthdays of different neuronal populations. To label proliferating cells in the embryonic nervous system, we injected pregnant rats on two consecutive days with 3H-thymidine. To label proliferating cells in the infant, juvenile, and adult nervous systems, we injected 3 H-thymidine on two to four consecutive days. The embryonic, infant, and juvenile animals survived to 60 postnatal days; by that time neurons are settled in the parenchyma and can be easily identified. The changes in the percentage of labeled and unlabeled neurons over a series of injection groups allowed us to accurately calculate the proportion of neurons generated on a single day in a given population. But how are we to date neurogenesis in the human nervous system? No experimental manipulation can be done. What can be done, however, is to apply the experimentally obtained data in rats to humans by matching their morphological appearance at different stages of development. During this matching procedure, we have found that morphological maturation of the spinal cord and brainstem are very similar in sequence. The exact chronology is different because days in rats translate to several days or a week in human development (Bayer et al., 1993). We have re-examined this chronological relationship in the new material presented in this Atlas. In the spinal cord (Altman and Bayer, 2001; Volume 1 of this Atlas; Bayer and Altman, 2002) the following developmental sequences can be matched between embryonic days (E) in rats and gestational weeks (GW) in humans: (i) expansion of stockbuilding NEP cells without differentiating neurons [E12=GW3.2], (ii) early motor neuron differentiation [E13=GW4.5], (iii) entry of dorsal root fibers into the spinal cord [E14=GW5.5], (iv) emergence of the dorsal root bifurcation zone [E16=GW7.0], and (v) formation of the dorsal funiculus [E18=GW8.5]. We have made similar comparisons in the rhombencephalon, mesencephalon, diencephalon, and telencephalon. For instance, the comparison of whole brain development in sagittal sections of rats and humans, (Figure 17A, B) suggests a chronological equivalence of E18=GW9.0, and the comparison of diencephalic and telencephalic development in coronal
TABLE 1
Developmental equivalance between rat and human CNS Rat
Human
(embryonic day)
(GW range)
11
<3.0-3.2
12
3.5-4.0
13
4.5-5.5
14
5.5-6.5
15
6.5-7.0
16
7.0-7.5
17
8.0-8.5
18
8.5-9.5
19
9.5-10
20
10.5-11
21
11.5-12
sections (Figure 17C, D) suggests a chronological equivalence of E18=GW9.2. The comparison of mesencephalic and rhombencephalic development shown in Figure 36 suggests a chronological equivalance of E15=GW7.0. In light of the small sample for comparison, we propose the human GW ranges to single E days in rats (Table 1); empirically based estimates are in bold. In contrast to the linear relationsip in brain development between E11-E21 prenatal rats and GW3-GW12 first trimester humans (Graph 1), there is no longer any linear relationship between postnatal (E22/P1+) rats and second and third trimester (GW13-GW37) humans. Whereas the newborn and infantile (preweaning, P1-P21) rat brain enters a period of quick maturation, the second and third trimester human brain retains its slow pace of prolonged development. This change in developmental tempo is par-
491
Graph 1
Neurogenesis continues in humans through the second trimester, third trimester, and postnatally.
12
or conjectural (red) estimates
Empirically based equivalences (green)
Trimesters 2 and 3
Postnatal
Human
11 10
Neurogenesis ceases in rats around weaning on postnatal day 21. Exceptions: adult neurogenesis in the dentate gyrus and the olfactory bulb
9 8 7 6 5 4
3 GW
E11 12 13 14 15 16 17 18 19 20 21
P21
Experimentally determined precise embryonic dates
Rat
ticularly pronounced in brain regions that differ markedly in size (and presumably in complexity) in rats and humans. For instance, in the cerebral cortex, the stratified transtional field (STF) is still prominint in the E20 rat but is in the process of dissolution two days later (E22) as birth is imminent (Altman and Bayer, 1995; the layer is labeled as “intermediate zone”). In sharp contrast, the STF remains as a prominent developmental structure in the greatly expanding human cortex from GW13.5 at the beginning of the second trimester (Volume 3 of this Atlas: Bayer and Altman, 2005) until GW26 at the beginning of the third trimester (Volume 2 of this Atlas: Bayer and Altman, 2004a); that is, for a period of over three months. On the basis of the several good matches between cytological and anatomical devel-
Rat
Rat
opment of the prenatal rat brain (in days) and the first trimester human brain (in weeks), we extrapolated neurogenetic timetable data in rats to the estimated time in humans for many CNS structures (Tables 2 through 7). Although we have quantitative data for the proportion of neurons generated on each particular day in the rat, we opted to conservatively extrapolate merely the time span of neurogenesis in the human brain. In very late-generated populations (granule cells of the cerebellar cortex, striatum, nucleus accumbens, microneurons in the upper layers of the cerebral cortex, and granule cells of the hippocampus), there is little equivalence other than the onset of neurogenesis. These timespans are marked with trailing arrows to indicate indeterminate cessation of neurogenesis.
492
TABLE 2
Spinal cord
Timespans of Neurogenesis Somatic motor neurons
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20 E21 Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5
9.5 10.5 11.5 10 11 12
Cervical Thoracic Lumbosacral
Thoracic visceral motor neurons Relay neurons (contralateral) Relay neurons (ipsilateral) Dorsal gray interneurons Hypoglossal nucleus (XII) Dorsal motor nucleus (X) Motor nucleus (VII) Abducens nucleus (VI)
Medulla and Pons
Motor nucleus (V) Mesencephalic (V) Spinal nucleus (V) Gracile nucleus Cuneate nucleus Solitary nucleus Vestibular complex Superior olive Cochlear nuclei Locus coeruleus Medullary and pontine reticular formation Medullary and pontine raphe complex Precerebellar nuclei are listed with the cerebellum in Table 6.
Motor structures Sensory structures Intercalated structures
493
TABLE 3 Timespans of Neurogenesis
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20 E21 Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5
9.5 10.5 11.5 10 11 12
Mesencephalic tegmentum
Trochlear nucleus (IV) Oculomotor complex (III) Edinger-Westphal nucleus (III) Parabigeminal nucleus Red nucleus
Magnocellular Parvocellular
Interpeduncular nucleus Raphe complex Central gray (ventral and lateral) Central gray (dorsal) Substantia nigra
Mesencephalic tectum
Ventral tegmental area Intermediate magnocellular layer Superior Layers V-VII colliculus Layers I-IV Lateral Inferior colliculus
Intermediate Anteromedial Posteromedial Motor structures Sensory structures Intercalated structures
494
TABLE 4
Timespans of Neurogenesis
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20 E21 Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5
9.5 10.5 11.5 10 11 12
Lateral geniculate (dorsal and ventral) Medial geniculate
Thalamus
Ventrobasal (lateral) Ventrobasal (medial) Reticular Anterior complex Dorsomedial Paraventricular Parafascicular Reuniens and rhomboid Lateral area Anterobasal
Hypothalamus
Suprachiasmatic Supraoptic Paraventricular Arcuate Ventromedial Dorsomedial Premammillary Supramammillary Tubero-mammillary Lateral mammillary Medial mammillary (dorsal) Medial mammillary (ventral)
Preoptic area
Lateral area Medial area Medial preoptic nucleus Sexually-dimorphic nucleus Periventricular nucleus Median preoptic nucleus Functionally different systems alternate in dark and light green
495
TABLE 5 Timespans of Neurogenesis
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20 E21 Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5
9.5 10.5 11.5 10 11 12
Cerebral Cortex
Cajal-Retzius neurons (I) Layers IV-II Inside-out gradient
Neocortex and limbic cortex
Layer V Layer VI
Subplate neurons (VII) Inside-out gradient
Primary olfactory cortex
Layer II Layers III-IV
Entopeduncular nucleus
Pallidum
Globus pallidus Substantia innominata
Basal telencephalon
Basal telencephalon/basal ganglia
Basal nucleus of Meynert Caudoputamen complex
Striatum
Nucleus accumbens Medial septal nucleus Diagonal band of Broca (vertical limb)
Septum
Lateral septal nucleus Bed nucleus of the stria terminalis Anterior amygdaloid area Central nucleus Medial nucleus Anterior cortical nucleus Amygdala
Posterior cortical nucleus Basomedial nucleus Basolateral nucleus Lateral nucleus Intercalated masses Amygdalo-hippocampal area Functionally different systems alternate in dark and light green Extended neurogenesis in humans
496
TABLE 6 Timespans of Neurogenesis
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20
E21 E22
Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5 10.5 11.5 9.5 10 11 12
P1 P3
P4 P7
P8 P11
P12 P15
P16 P19
No equivalence during the second and third trimesters
Cerebellum
Deep nuclei Purkinje cells Golgi cells Basket cells Stellate cells
Precerebellar nuclei
Granule cells Inferior olive Lateral reticular nucleus Reticular tegmental nucleus Pontine gray Functionally different systems alternate in dark and light green Extended neurogenesis in humans
TABLE 7 Timespans of Neurogenesis
Experimentally determined data in rats (in days)
E11 E12 E13 E14 E15 E16 E17 E18 E19 E20
E21 E22
Estimated time of development in humans in weeks (GW)
3.0 3.2
3.5 4.0
4.5 5.5
5.5 6.5
6.5 7.0
7.0 7.5
8.0 8.5
8.5 9.5 10.5 11.5 9.5 10 11 12
P1 P3
P4 P7
P8 P11
P12 P15
P16 P19
No equivalence during the second and third trimesters
Layer II Layer III
Entorhinal cortex
Layer IV Layers V-VI
Parasubiculum (superficial) Inside-out gradient
Hippocampal region
Inside-out gradient
Subiculum proper (superficial) Presubiculum (superficial) Presubiculum and Parasubiculum (deep)
Subiculum
Subiculum proper (deep) Field CA1 Ammon's horn
Field CA3ab
Hippocampus
Field CA3c Dentate granule cells Functionally different systems alternate in dark and light green Extended adult neurogenesis in both humans and rats
497
498
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Altman, J. and S. A. Bayer (1978a) Prenatal development of the cerebellar system in the rat. I. Cytogenesis and histogenesis of the deep nuclei and the cortex of the cerebellum. Journal of Comparative Neurology, 179:23-48. Altman, J. and S. A. Bayer (1978b) Prenatal development of the cerebellar system in the rat. II. Cytogenesis and histogenesis of the inferior olive, pontine gray, and the precerebellar reticular nuclei. Journal of Comparative Neurology, 179:49-76. Altman, J. and S. A. Bayer (1978c) Development of the diencephalon in the rat. I. Autoradiographic study of the time of origin and settling patterns of neurons of the hypothalamus. Journal of Comparative Neurology, 182:945-972. Altman, J. and S. A. Bayer (1978d) Development of the diencephalon in the rat. II. Correlation of the embryonic development of the hypothalamus with the time of origin of its neurons. Journal of Comparative Neurology, 182:973-994. Altman, J. and S. A. Bayer (1978e) Development of the diencephalon in the rat. III. Ontogeny of the specialized ventricular linings of the hypothalamic third ventricle. Journal of Comparative Neurology, 182:995-1016. Altman, J. and S. A. Bayer (1979a) Development of the diencephalon in the rat. IV. Quantitative study of the time of origin of neurons and the internuclear chronological gradients in the thalamus. Journal of Comparative Neurology, 188:455-472. Altman, J. and S. A. Bayer (1979b) Development of the diencephalon in the rat. V. Thymidine-radiographic observations on internuclear and intranuclear gradients in the thalamus. Journal of Comparative Neurology, 188:473-500. Altman, J. and S. A. Bayer (1979c) Development of the diencephalon in the rat. VI. Re-evaluation of the embryonic development of the thalamus on the basis of thymidineradiographic datings. Journal of Comparative Neurology, 188:501-524. Altman, J. and S. A. Bayer (1980a) Development of the brain stem in the rat. I. Thymidine-radiographic study of the time of origin of neurons of the lower medulla. Journal of Comparative Neurology, 194:1-35. Altman, J. and S. A. Bayer (1980b) Development of the brain stem in the rat. II. Thymidine-radiographic study of the time of origin of neurons of the upper medulla, excluding the vestibular and auditory nuclei. Journal of Comparative Neurology, 194:37-56 Altman, J. and S. A. Bayer (1980c) Development of the brain stem in the rat. III. Thymidine-radiographic study of the time of origin of neurons of the vestibular and auditory nuclei of the upper medulla. Journal of Comparative Neurology, 194:877-904. Altman, J. and S. A. Bayer (1980d) Development of the brain stem in the rat. IV. Thymidine-radiographic study of the time of origin of neurons in the pontine region. Journal of Comparative Neurology, 194:905-929.
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Altman, J. and S. A. Bayer (1988a) Development of the rat thalamus. I. Mosaic organization of the thalamic neuroepithelium. Journal of Comparative Neurology, 275:346-377. Altman, J. and S. A. Bayer (1988b) Development of the rat thalamus. II. Time and site of origin and settling pattern of neurons derived from the anterior lobule of the thalamic neuroepithelium. Journal of Comparative Neurology, 275:378-405. Altman, J. and S. A. Bayer (1988c) Development of the rat thalamus. III. Time and site of origin and settling pattern of neurons of the reticular nucleus. Journal of Comparative Neurology, 275:406-428.
Altman, J. and S. A. Bayer (1982a) Morphological development of the rat cerebellum and some of its mechanisms. In: S. L. Palay and V. Chan-Palay (eds.). The Cerebellum: New Vistas, pp. 8-49. Berlin: Springer-Verlag.
Altman, J. and S. A. Bayer (1989a) Development of the rat thalamus. IV. The intermediate lobule of the thalamic neuroepithelium, and the time and site of origin and settling pattern of neurons of the ventral nuclear complex. Journal of Comparative Neurology, 284:534-566.
Altman, J. and S. A. Bayer (1982b) Development of the Cranial Nerve Ganglia and Related Nuclei in the Rat. (Advances in Anatomy, Embryology and Cell Biology, Vol. 74). Berlin: Springer-Verlag.
Altman, J. and S. A. Bayer (1989b) Development of the rat thalamus. V. The posterior lobule of the thalamic neuroepithelium and the time and site of origin and settling pattern of neurons of the medial geniculate body. Journal of Comparative Neurology, 284:567-580.
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GLOSSARY GLOSSARY
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An asterisk in front of a term indicates that it is a separate entry in the Glossary with additional information. A
B
Abducens nucleus (VI) – An aggregate of cranial nerve motor neurons situated beneath the fourth ventricle in the *pons. The nucleus receives input from the *vestibular nuclear complex and is the source of motor fibers of cranial *nerve VI that innervate the lateral rectus muscle of the eye.
Basal ganglia – Large nuclear (subcortical) component of the telencephalon, including the *septum, the *striatum, the *nucleus accumbens, and the *globus pallidus.
Ammonic NEP – Subdivision of the *hippocampal NEP, the putative source of the pyramidal cells of Ammon’s horn. Amygdaloid NEP – Neuroepithelium lining the posteroventral *telencephalic superventricle, the presumptive site of origin of neurons and glia of the amygdala. It is continuous rostrally with the posterior *striatal NEP, laterally with the temporal NEP, and medially with the ventral *hippocampal NEP. Anterior extramural migratory stream – Large stream of young neurons that migrate from the *precerebellar NEP to the *pontine gray and the *reticular tegmental nucleus. The stream forms during the latter part of the late first trimester, after the settling of inferior olivary neurons that migrate in the *posterior intramural migratory stream. Anterior neuropore – The unfused *neural tube in the early *prosencephalon. It closes between GW3.2 and GW3.8. Anterior pituitary gland (embryonic) – The anterior lobe of the pituitary gland, also known as the adenohypophysis. It is derived from the invaginating *Rathke’s pouch, a midline portion of the *cephalic placode. Anterior precerebellar NEP – Neuroepithelial source of neurons of the *pontine gray and *reticular tegmental nucleus associated with the lower *rhombic lip. The neurons migrate to their target structures by way of the *anterior extramural migratory stream. Aqueduct (embryonic) – See Mesencephalic superventricle. Auditory-Vestibular NEP – See Rhombomeric NEPs
Basal ganglionic NEP and SVZ – Initially a single ventral telencephalic protuberance, the basal ganglionic NEP is partitioned into three large hillocks or eminences – the anterolateral, the anteromedial, and the posterior – protruding into the *telencephalic superventricle and produce the neuroepithelial and subventricular progenitor cells that furnish neurons and neuroglia to the *basal ganglia. A fourth component is the corticoganglionic NEP/SVZ that may generate cortical neurons. The SVZ is far more prominent in the basal ganglia than in the developing *cerebral cortex. Basal telencephalic NEP – Putative source of neurons and neuroglia of the basal nucleus of Meynert and the substantia innominata. Branchial arches – Mesenchymal pouches – including the mandibular arch (I), the hyoid arch (II), and the pharyngeal (post-oral, visceral) arches III-IV – that contribute to the formation of the mandible, the hyoid bone, parts of the ear, the thyroid cartilage, and some visceral structures. The branchial arches are believed to be phylogenetically derived from the gills of protochordates and lower vertebrates. Branchial placodes – Distinguished from the rostral *cephalic placodes, the caudal branchial placodes cover portions of the *branchial arches, the oral cavity, and the gullet. The pluripotent progenitor cells of the branchial placodes are the source of neurons of the cranial nerve ganglia, and may contribute the somatosensory elements of the head region, the gustatory system, and the acoustico-vestibular system. Boundary cap – A thin ring of proliferative cells surrounding the spinal and cranial nerves at the site they enter the CNS. It is presumed to be a source of Schwann cells of peripheral nerves. C Cajal-Retzius cells – Unique neurons with perikarya oriented parallel to the pial surface in the *primordial plexiform layer of the developing *cerebral cortex.
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GLOSSARY Central canal (embryonic) – Portion of the ventricular system continuous with the *rhombencephalic superventricle. It extends from the cervical to the sacral segments of the spinal cord. During embryonic development, the proliferative NEP matrix lining this canal is the source of neurons and neuroglia of the spinal cord. After the cessation of neurogenesis, the shrunken central canal is lined by the *ependyma.
Cerebellar transitional field (CTF) – Transient cellular and fibrous layers, composed of migrating deep neurons and Purkinje cells, and of exiting and entering fiber tracts, prior to the formation of the *cerebellar cortex.
Cephalic placodes – Distinguished from the *branchial placodes, part of the *preplacode, that will become subdivided into the *olfactory placode, the *optic (lens) placode, and the *pituitary placode (*Rathke’s pouch). The cephalic placode, composed of pluripotent progenitor cells, is continuous with the *prosencephalic NEP before it fuses.
Cerebral cortex (embryonic) – The expanding and differentiating bilateral brain region covering the lateral, dorsal, and medial aspects of the *telencephalic superventricles. It has three major components, the *neocortex, the *limbic cortex, and the *primary olfactory cortex. The neurons generated by the cortical NEPs initially form the *stratified transitional field and the *cortical plate.
Cephalic vesicles – NEP divisions of the head region, initially composed of the *prosencephalon, *mesencephalon, and *rhombencephalon. Early during embryonic development, the prosencephalon becomes divided into the bilateral telencephalon and the medial diencephalon. Cerebellar cortex (embryonic) – Begins to form after the spreading *external germinal layer (EGL) forms a canopy over the surface of the cerebellum and the *Purkinje cells begin to line up beneath the EGL. The embryonic cerebellar cortex is devoid of microneurons (granule, basket, and stellate cells) and lacks a differentiated granular and molecular layer. Cerebellar deep nuclei – Three pairs of ganglionic structures beneath the *cerebellar cortex: the medial *fastigial nucleus; the intermediate *interpositus nucleus, and the lateral *dentate nucleus. The efferent fibers of cerebellar *Purkinje cells synapse with the neurons of the cerebellar deep nuclei which, in turn, are the source of cerebellofugal fibers that terminate in structures outside the cerebellum. The early-generated deep nuclei neurons initially sojourn superficially in the *nuclear transitional zone of the formative cerebellum. Cerebellar hemisphere – Portion of the cerebellum flanking the medial *vermis. It is particularly large in higher mammals and humans. Cerebellar NEP – An extensive neuroepithelial matrix that initially forms the upper *rhombic lip. It is the direct source of the neurons of the *cerebellar deep nuclei and the *Purkinje cells, and an indirect source of the basket, stellate, and granule cells, which are produced by a secondary proliferative matrix, the *external germinal layer.
Cerebellar vermis – Medial portion of the cerebellum. It is relatively small in higher mammals and man.
Choroid plexus (embryonic) – Glycogen-rich epithelial tissue that forms during the early first trimester and begins to expand during the late first trimester in the *rhombencephalic superventricle and the *telencephalic superventricle. It is formed by proliferative stem cells associated with the cerebellar *germinal trigone and an analogous germinal site in the *hippocampus. The fetal choroid plexus may play a role in the anaerobic metabolism of the early developing brain. During late-fetal development, it becomes gradually transformed into the mature choroid plexus of the shrunken lateral and fourth ventricles, with a different cellular composition and presumably a different function. Cingulate NEP – Extensive neuroepithelial matrix in the *limbic cortex along the medial wall of the *telencephalic superventricle above the *septum and *hippocampus. It generates the neurons and neuroglia of the cingulate cortex. Cochlear NEP – Neuroepithelial matrix in the vicinity of the lower *rhombic lip, the putative source of neurons and neuroglia of the ventral and dorsal *cochlear nuclei. Cortical NEP – An extensive and continuous neuroepithelial matrix lining of the lateral, dorsal, and medial banks of the *telencephalic superventricle; major subdivisions are the *neocortical NEP, *limbic cortical NEP, and the *primary olfactory cortical NEP. It is the sole constituent of the *cerebral cortex during the early embryonic period. Following a strict timetable and spatial gradient, it expands and then shrinks as classes of differentiating neurons and glia leave it to enter the *stratified transitional field and migrate to the *cortical plate. The cortical NEP is also the source of a secondary proliferative matrix, the *subventricular zone, of fate-restricted *glioepithelia and
GLOSSARY neurons, and the cells that line the enduring *ependyma of the lateral ventricles. Cortical plate – The densely packed cellular band in the embryonic and fetal *cerebral cortex that later becomes the stratified *gray matter of cortical layers II-VI. It is situated between the *primordial plexiform layer (future layer I) and the subplate (future layer VII). Cortical transition zone (cerebellum) – Deep sojourn zone of young *Purkinje cells before they begin their ascent toward the surface to form the cerebellar cortex. Corticofugal fibers (embryonic) – Collective term for the efferent fiber system (the traditional pyramidal tract) that originates in the cerebral cortex and terminates in subcortical structures. It is known by different names along its path from rostral to caudal: *internal capsule, cerebral peduncle, *transpontine corticofugal tract, and corticospinal tract. The corticofugal tract begins to form during the end of the late first trimester but its fibers do not reach the spinal cord until the end of the second trimester. D Dentate gyrus – Component of the *hippocampus, composed of granule cells and interlocked with the largecelled *Ammon’s horn. Although the *dentate migration is recognizable by the end of the first trimester, the blades of the dentate gyrus do not form until the second trimester.
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erally symmetrical evaginations or invaginations and variable cell-depth, are the source of neurons and neuroglia of the different nuclei of the *diencephalon. Diencephalic superventricle – Large midline component of the embryonic ventricular system that is later reduced to the narrow third ventricle. It is confluent laterally, by way of the foramen of Monro, with the *telencephalic superventricle, and caudally with the *mesencephalic superventricle. Its lining, the *diencephalic NEP, is the source of all the neurons and neuroglia of the *diencephalon. Diencephalon (embryonic) – Extensive forebrain region flanked laterally by the telencephalon and continuous caudally with the mesencephalon. Among its larger components are the *epithalamus and the *thalamus dorsally; the *optic vesicle, the *preoptic area, the *hypothalamus, and the *subthalamus ventrally. Its parenchymal development precedes that of the dorsal *telencephalon. Dorsal rhombic lip – see Rhombic lip, upper. E Ependyma – Layer of cuboidal cells that line the lumen of the permanent brain *ventricles and *central canal after dissolution of the proliferative *neuroepithelium. Epithalamic NEP – Neuroepithelial division of the *diencephalic NEP, the putative source of neurons and neuroglia of the *epithalamus.
Dentate migration – Precursors of granule cells of the *dentate gyrus that leave the *dentate NEP to form what will later become the secondary germinal matrix of the hippocampus, the *subgranular zone.
Epithalamus – Collective term for the region of the dorsal diencephalon consisting of the habenular nuclei, the stria medullaris, and the habenulo-interpeduncular tract.
Dentate NEP – Division of the *hippocampal NEP that is the source of the progenitor cells of the *dentate migration and the *subgranular zone.
External germinal layer (EGL) – Subpial, secondary germinal matrix of the cerebellar cortex, the source of its late-differentiating granule, stellate, and basket cells. It begins to form during GW8 and persists as a source of neurons over the surface of the human cerebellar cortex until the end of the second year of postnatal life.
Dentate nucleus (embryonic) – The lobulated and largest of the *cerebellar deep nuclei in the core of the *cerebellar hemisphere, it is the principal source of efferent fibers of the superior cerebellar peduncle. In the embryonic cerebellum, the early-generated neurons of the dentate nucleus are situated superficially and do not descend until after the late-generated *Purkinje cells migrate toward the surface to form the cerebellar cortex. Diencephalic NEP – An extensive neuroepithelial matrix lining the midline *diencephalic superventricle. Its different mosaic components, distinguished by bilat-
F Facial ganglion – A small clump of peripheral sensory neurons located in the hyoid arch slightly below and anterior to the large vestibulocochlear ganglion. It is the source of the sensory axons in nerve VII that carry taste information from the anterior tongue and enter the brain in the posterior rhombomere 3. These neurons are presumably generated by the neural crest and
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GLOSSARY by germinal cells in a branchial placode in the hyoid arch. Facial motor nucleus – A large aggregate of somatic motor neurons in the posterior pons and anterior medulla. It is the source of the motor fibers of *nerve VII that innervate the facial mimetic muscles. Facial NEP – See Rhombomeric NEPs. Fastigial nucleus (cerebellum) – A deep nucleus of the *cerebellum, also known as the medial cerebellar nucleus. It is the target of Purkinje cell axons that originate in the *vermis. Its axons contribute to the large efferent system that leaves the cerebellum. Foramen of Monro (embryonic) – Bilateral channels that connect the paired *telencephalic superventricles with the midline * diencephalic superventricle. Fornical GEP – Fate-restricted germinal extension of the hippocampal NEP, the *glioepithelium that surrounds the fornix. It may be the germinal source of the oligodendrocytes of the fornix. Fornix – An early forming fiber tract of the *hippocampus that distributes fibers in the mature brain to the septum and the anterior thalamic nuclei, and terminates in the mammillary body. Fourth ventricle (embryonic) – See Rhombencephalic superventricle. G Germinal trigone (cerebellum) – Proliferative germinal matrix of the upper *rhombic lip with three prongs: the *cerebellar NEP, the *external germinal layer, and the stem cells of the rhombencephalic *choroid plexus. Glioepithelium (GEP) – Fate-restricted transient germinal matrix in the developing CNS, the presumed source of astrocytes and oligodendroglia. There are two types of glioepithelia, the *perifascicular GEP that surrounds fiber tracts, such as the *fornical GEP, and another that covers the surface of the brain, the *subpial granular layer. Glioepithelia are easiest to recognize without special glial markers at sites of considerable distance from neuronal aggregates or their migratory routes. Glioepithelium/Ependyma (G/EP) – Transient proliferative lining of the ventricle that endures into adulthood and gives rise to both neuroglia and cells of the *ependyma.
Glossopharyngeal ganglia – Superior and inferior clumps of peripheral sensory neurons located in arch III and behind the otic vesicle. These ganglia are the source of nerve IX sensory axons that enter the brain at rhombomere 6 carrying taste and visceral sensory information. These neurons are presumably generated by cells in the neural crest and by a placode in arch III. Glossopharyngeal NEP – See Rhombomeric NEPs. Gray matter – General term for the component of the mature CNS with a high concentration of neuronal cell bodies and nerve processes but few myelinated fibers. H Hippocampal NEP – Medial matrix of the *cortical NEP, the putative neuroepithelial source of the neurons and neuroglia of the hippocampus. It has three distinctive parts, the *Ammonic NEP, the *dentate NEP, and the *fornical GEP. Hippocampal region – An inclusive term (also called the hippocampal formation) that includes not only the *hippocampus proper but also the *subicular complex and other components of the parahippocampal cortex. Hippocampus – A distinctive allocortical (oligolaminar) region formed by the interlocking *dentate gyrus and Ammon’s horn. The principal afferents of the hippocampus travel in the alveolar and perforant paths; its efferents leave by way of the *fornix. Honeycomb matrix – A layer in the *stratified transitional field, composed of radially oriented fibers surrounded by concentrically arranged cells. It is prominent in the sensory areas of the developing *cerebral cortex, and may also be present in the *superior colliculus. The fibers are hypothesized to be topographically organized. Hook bundle (embryonic) – Intracerebellar commissural tract that originates in the *cerebellar deep nuclei and is presumed to leave the crebellum contralaterally as the uncinate fasciculus. A prominent fibrous region identified at the base of the cerebellum in GW8-GW9 specimens may be the sprouting fibers of this tract. Hypothalamic NEP – Ventral division of the *diencephalic NEP, situated posterior to the preoptic NEP. It is the source of neurons and neuroglia of the nuclei of the *hypothalamus.
GLOSSARY Hypothalamus (embryonic) – Early-differentiating, large diencephalic region that surrounds the ventral division of *diencephalic superventricle. It is continuous anteriorly with the *preoptic area and merges caudally with the midbrain *tegmentum. The hypothalamus contains a large number of discrete nuclei that link the forebrain with the autonomic nervous system and the endocrine system. I Inferior collicular NEP – Distinctive neuroepithelial division of the *tectal NEP surrounding the posterior pool of the *mesencephalic superventricle, and the source of neurons of the *inferior colliculus. Inferior colliculus – Paired posterior hillocks of the midbrain *tectum that receive primary, secondary, and higher order auditory afferents. The output of the inferior colliculus is mainly to the *medial geniculate nucleus in the thalamus. Inferior olive (embryonic) – A compact cell aggregate in the lower *medulla, formed by neurons of the *posterior intramural migratory stream during the late first trimester. Its lamination does not begin until the end of the second trimester. Infundibular recess – Small recess of the third ventricle that evaginates into the *infundibulum and is closely associated with the *pituitary placode (Rathke’s pouch). Infundibulum – Stalk extending from the ventral *hypothalamus that forms a link with the pituitary gland. Insular cortex – Early maturing part of the lateral limbic cortex located above the neocortex of the future temporal lobe. This area of cortex is the first to have a cortical plate that appears on GW7.5. Early thalamocortical fibers and other pioneer cortical afferents invade the cortex here. Interhemispheric fissure – Longitudinal cleft that separates the two cerebral hemispheres. The corpus callosum that traverses it in the maturing brain starts to form at the beginning of the second trimester. Intermediate zone – See Stratified transitional field. Internal capsule (embryonic) – Massive fiber tract between the thalamus and cortex, composed of *thalamocortical fibers and *corticofugal fibers. It is beginning to form at about GW8 as the earliest thalamocortical fibers cross into the telencephalon.
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Interpositus nucleus (cerebellum) – A deep cerebellar nucleus located between the *dentate nucleus and the *fastigial nucleus. Isthmal canal – Channel that interconnects the *mesencephalic superventricle and the *rhombencephalic superventricle. Isthmal NEP – The putative source of neurons and neuroglia of the transient *isthmus region. Isthmus – Transient mesencephalic region that surrounds the isthmal canal, situated caudal to the tectum and tegmentum, and rostral to the rhombencephalon. Most of the neurons generated at this site migrate to other, as yet undetermined, regions of the pons and midbrain. L Lateral geniculate nucleus (embryonic) – The neurons of this prominent thalamic nucleus appear to be generated dorsally in a distinct neuroepithelial locus and migrate ventrolaterally where they meet the fibers of the incoming *optic tract. Lateral hypothalamic area – An ill-defined fibrous region of the *hypothalamus with scattered neurons medial to the cerebral peduncle. It is traversed by many fiber tracts, including the *medial forebrain bundle. Lateral lemniscus – The fiber tract on the lateral surface of the *pons that contains secondary auditory fibers from the dorsal and ventral cochlear nuclei and higherorder auditory fibers from the superior olivary complex. Lateral migratory stream (cortical) – Tangentially migrating neurons and glia in the developing *cerebral cortex that leave dorsal *cortical NEP and migrate laterally and ventrally to the insula, the *temporal lobe, and other telencephalic structures that lack a nearby germinal matrix. The bulk of the lateral migratory stream follows a trajectory outlined by the receding *subventricular zone between the basal ganglia and the lateral cortex. Lateral ventricles – See Rhombencephalic superventricle Layer I, cortical (embryonic) – See Primordial plexiform layer. Lens placode – Fate-restricted portion of the *cephalic placode whose progenitor cells will produce the crystalline lens of the eye.
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GLOSSARY Limbic cortex – Portion of the cerebral hemispheres that, in contrast to the *neocortex, contains fewer than six definite cellular layers. Among prominent limbic regions are the cingulate gyrus, hippocampus, entorhinal cortex, and insula. Limbic cortical NEP – Portion of the *cortical NEP that generates neurons in the *cingulate gyrus, *hippocampus, *entorhinal cortex, and *insular cortex. This part of the cortical NEP forms a lateral and medial border around the *neocortical NEP. Luysiian migration – The intramural migratory stream of subthalamic nuclear neurons (corpus Luysii) has been traced from the region of the formative mammillary body medially to the subthalamus dorsolaterally. M Maxillary process – A swelling in the embryonic head located behind the invaginating olfactory placode that contains the primordium of the maxilla. Medial forebrain bundle – A diffuse fiber tract that extends from the olfactory region, through the *lateral hypothalamic area, to the *substantia nigra in the midbrain *tegmentum. Medial geniculate nucleus – Principal thalamic relay station in the auditory pathway to the *cerebral cortex. Its afferents originate in the *trapezoid body, the *superior olivary complex, the *nuclei of the lateral lemniscus, and the *inferior colliculus. Its efferents form the auditory radiation that terminates in the *temporal lobe. Medial lemniscus – Large fiber bundle conveying tactile and other somatosensory input to the thalamus. It originates in the gracile and cuneate nuclei in the *medulla, crosses to the opposite side, ascends through the *pons and the *mesencephalon, and terminates in the somatosensory relay nuclei of the thalamus (ventral complex). Medial lemniscus (decussation) – Also known as the arcuate decussation, it is composed of ascending somatosensory fibers of the medial lemniscus that cross to the opposite side in the medulla. Medial longitudinal fasciculus – A dorsomedial tract in the *mesencephalon, *pons, and *medulla that contains ascending and descending vestibular fibers coursing in the medial tegmentum and pons, turns ventrally in the posterior *medulla and extends into the ventral funiculus of the cervical spinal cord.
Medulla (embryonic) – Early-generated region of the brain that is continuous with the spinal cord, also known as the medulla oblongata. This extremely heterogeneous region surrounds the posteroventral *rhombencephalic superventricle and contains sensory, somatomotor, and visceromotor nuclei as well as several ascending, descending, and decussating fiber tracts. Medullary NEP – Extensive neuroepithelial matrix that lines the variegated caudal bank of the *rhombencephalic superventricle. Its several subdivisions are the source of neurons and neuroglia of the different sensory, relay, and motor nuclei of the *medulla. Medullary velum – Membranous roof of the *rhombencephalic superventricle that extends from the upper to the lower *rhombic lips. It is the only site in the CNS where the neural tube fails to fuse. A portion of its inner surface contains stem cells for the rhombencephalic choroid plexus. Mesencephalic NEP – The extensive neuroepithelium that lines the large *mesencephalic superventricle. Its major divisions are, from rostral to caudal, the *pretectal NEP, the *tectal NEP, the *tegmental NEP, and the *isthmal NEP. Subdivisions of the tectal NEP are the NEPs of the *superior colliculus and *inferior colliculus. Subdivisions of the tegmental NEP are the NEPs of the *oculomotor nucleus, the *red nucleus, and other structures of the *tegmentum. Mesencephalic superventricle – Greatly inflated lumen of the embryonic *mesencephalon, situated between the *diencephalic superventricle rostrally and the *rhombencephalic superventricle caudally. The connection with the latter is by way of the *isthmal canal. It shrinks in the maturing brain into the small and narrow aqueduct. Mesencephalon (embryonic) – Region of the brainstem that surrounds the *mesencephalic superventricle and forms a bridge between the *pons and the *diencephalon. Among its early-differentiating components are the pretectum with the *posterior commissure, the *oculomotor nucleus and the *trochlear nucleus, and neurons of the *reticular formation. Meyer’s loop – Part of the *visual radiation that takes a sharp curve in the *temporal lobe as it proceeds to the occipital lobe. It is recognizable by GW11. Microneurons – Late-generated small neurons (“granule cells”) with locally arborizing axons that form discrete layers in several cortical structures or become embedded within nuclear structures. Microneurons are produced by *secondary germinal matrices, such
GLOSSARY as the *subventricular zone of the cerebral cortex and striatum, the *subgranular zone of the hippocampus, and the *external germinal layer of the cerebellum. A high proportion of cerebellar granule cells are generated during the first years of life, and the granule cells of the olfactory bulb and the dentate gyrus are generated from fetal stages through adulthood. Midbrain – See Mesencephalon. N Neocortex (embryonic) – Portion of the cerebral hemispheres that develops into a “six-layered” cortical *gray matter. Neocortical development begins with the expansion of the primordial *cortical NEP devoid of differentiated neurons. Next comes the formation of the *primordial plexiform layer. Then the *cortical plate appears along with different layers in the *stratified transitional field (*intermediate zone), and the *subventricular zone. The principal divisions of the neocortex are the frontal lobe, the paracentral lobule, the parietal lobe, the temporal lobe, and the occipital lobe. Neocortical NEP – Extensive neuroepithelium that lines the lateral and dorsal aspects of the *telencephalic superventricles. The proliferating neocortical NEP cells are the source of neurons and neuroglia that migrate to the *cortical plate by way of the *stratified transitional field. Some of its cells may move to more distant sites by way of the *lateral migratory stream. It is bordered medially and laterally by the *limbic cortical NEP. Nerve I – See Olfactory nerve. Nerve II – See Optic nerve. Nerve III (oculomotor) – Cranial motor nerve originating in the *oculomotor nucleus. It innervates all the extraocular muscles (except the lateral rectus and superior oblique), the skeletal muscles of the eyelid, the smooth sphincter muscles of the iris, and the ciliary muscles of the lens. Nerve IV (trochlear) – Cranial motor nerve composed of axons of the *trochlear nucleus that innervates the superior oblique muscle of the eye. This nerve is unique because it exits from the dorsal surface of the *mesencephalon beneath the *inferior colliculus. Nerve V (trigeminal)– A mixed sensory and motor cranial nerve that has three peripheral branches: the ophthalmic, the maxillary, and the mandibular. All three branches contain peripheral sensory fibers from the *trigeminal ganglion that terminate in the trigemi-
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nal principal sensory nucleus, the *trigeminal spinal nucleus, and the substantia gelatinosa in upper cervical segments of the spinal cord. A bundle of fibers in the mandibular branch, originating in the *trigeminal motor nucleus, innervates the muscles of mastication. Nerve VI (abducens) – Cranial motor nerve that originates in the abducens nucleus and emerges near the midline at the caudal border of the pons. The fibers innervate the lateral rectus muscle of the eye. Nerve VII (facial) – A mixed sensory and motor nerve, the facial nerve has three components. Primary sensory gustatory fibers from the geniculate ganglion enter the solitary tract and nucleus. Somatic motor fibers from the *facial motor nucleus innervate the mimetic muscles. Visceral motor (parasympathetic) fibers from preganglionic neurons of the salivatory nucleus target the pterygopalatine and submandibular ganglia. Nerve VIII (vestibulo-cochlear) – A sensory cranial nerve that contains primary auditory afferents from the spiral ganglion in the cochlea and primary vestibular afferents from the vestibular (Scarpa’s) ganglion. Embryonically, both of these ganglia form the large *vestibulo-cochlear ganglion adjacent to the *otic vesicle. The auditory afferents terminate in the dorsal and ventral cochlear nuclei; the vestibular afferents terminate in the nuclei of the vestibular nuclear complex and some reach the cerebellum. Nerve IX (glossopharyngeal) – A mixed sensory and motor cranial nerve. The sensory part originates in the superior and inferior *glossopharyngeal ganglia, and relays gustatory input from the posterior third of the tongue and visceral sensory input from the tonsils, the Eustachian tube, and the carotid sinus. These fibers enter the solitary tract and terminate in the solitary nucleus. The somatic motor part of nerve IX originates in the nucleus ambiguus and innervates the pharyngeal and laryngeal muscles. The visceral motor fibers from parasympathetic preganglionic neurons in the salivatory nucleus terminate in the otic ganglion. Nerve X (vagus) – A mixed sensory and motor cranial nerve, with some somatic and many visceral afferents and efferents associated with the craniosacral parasympathetic ganglia. The sensory fibers originate peripherally in the superior and inferior ganglia and are widely distributed throughout the body, including the pharynx, larynx, trachea, esophagus, and all the thoracic and abdominal viscera. They terminate centrally in the solitary nucleus and at other medullary sites. Most of its preganglionic motor neurons are located in the dorsal motor nucleus of X.
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GLOSSARY Nerve XI (accessory) – This motor nerve has a cranial and a spinal component. The cranial fibers originate in the nucleus ambiguus and innervate the muscles of the larynx and pharynx. The spinal motor fibers originate in a motor column of the cervical spinal cord and innervate the sternocleidomastoid and upper trapezius muscles. Early in embryonic life this nerve is seen along the superficial border of the superior *vagal ganglion. Nerve XII (hypoglossal) – A somatic motor cranial nerve that originates in the *hypoglossal nucleus and innervates the intrinsic and extrinsic muscles of the tongue. Neural plate – Matrix of pluripotent stem cells of the early embryo that gives rise to neural crest cells and the *neuroepithelium. Neuroepithelium (NEP) – Pseudostratified matrix of neural stem cells, the source of all neurons and neuroglia of the developing CNS. The NEP matrix begins its developmental career as the *neural plate. The neural plate folds dorsally and fuses to form, caudally, the neural tube (future spinal cord) and, rostrally, the *cephalic vesicles (the future brain). After closure, the lumen of the cephalic vesicles expands enormously to form the *rhombencephalic, *mesencephalic, *diencephalic, and *telencephalic superventricles. This expansion provides the space for the mitotic division of NEP cell nuclei that must shuttle to the fluid-filled lumen to undergo mitosis. Two NEP matrices are distinguished, the early-phase *stockbuilding NEP that only produces proliferative daughter cells, and the later-phase NEP that produces daughter cells that leave the NEP matrix. The continuous but variegated cephalic NEP matrix lining the ventricles have a mosaic organization, being composed of bilaterally symmetrical long stretches, and of intermediate or shorter patches that give rise to neurons and neuroglia of different brain regions, distinct brain structures, and specific cell types. Examples of long stretches are the *cortical NEP and the *cerebellar NEP. Examples of intermediate patches are the *thalamic NEP and the *hypothalamic NEP of the inclusive *diencephalic NEP. Examples of short patches are the *Ammonic NEP and *dentate NEP of the inclusive *hippocampal NEP. The primary NEP matrix is also the source of several *secondary germinal matrices that generate *microneurons with locally arborizing axons. Finally, as neurogenesis winds down, the pluripotential NEP is transformed at many sites into a *glioepithelium, such as the *fornical GEP, or into the *ependyma that lines the enduring ventricles.
Nuclear transition zone (cerebellum) – Superficial sojourn site in young embryos, composed of the early-generated deep nuclear neurons. These neurons migrate to a deep position within the cerebellum as the later-generated Purkinje cells that sojourn in the *cortical transition zone migrate toward the surface to form a monolayer there. Nucleus accumbens – Ganglionic component of the ventral telencephalon ventromedial to the striatum. It is distinguished from the striatum by its cellular organization, molecular composition, and intimate connections with the hypothalamus, amygdala, and other regions of the limbic system. O Occipital NEP – Putative neuroepithelial division of the neurons and neuroglia of the occipital lobe. It is the target of *visual radiation fibers from the *lateral geniculate nucleus. Oculomotor nerve – See Nerve III. Oculomotor nucleus – Early-forming medial structure in the anterior mesencephalic tegmentum that is the source of the fibers of cranial *nerve III. Olfactory bulb – Laminated brain structure where the first-order fibers of the *olfactory nerve terminate and the second-order fibers of the olfactory tract originate. It is composed of three classes of neurons: the earlygenerated large mitral cells, the intermediate tufted cells, and the late-generated small granule cells. Olfactory bulb NEP – This NEP evaginates into the telencephalic area that is contacted by olfactory nerve axons, forming the olfactory recess. It generates some of the neurons in the olfactory bulb; the latergenerated granule cells are supplied by the *rostral migratory stream. Olfactory cortical NEP – This NEP is located near the *olfactory bulb NEP anterolateral to the basal telencephalic NEP. It generates some of the neurons in the *primary olfactory cortex. Olfactory nerve (embryonic) – Composed of the fine axons of bipolar neurons in the olfactory epithelium that terminate in the *olfactory bulb. The sprouting nerve is recognizable as early as GW4. Olfactory placode – Fate-restricted portion of the *cephalic placode whose progenitor cells will produce the olfactory epithelium and the olfactory bipolar neurons. The olfactory placode may exert an inductive influence on the diversification of the olfactory NEP.
GLOSSARY Optic chiasm (embryonic) – Site of crossing of fibers of the *optic nerve. Fibers from the nasal half of each retina cross here to the opposite side while those from the temporal half proceed uncrossed. The earliest crossing fibers are seen in GW7.5 specimens. Optic nerve – Large fiber tract composed of the axons of retinal ganglion cells. Traditionally, the portion of the tract between the eye and the *optic chiasm is referred to as cranial nerve II. Optic (lens) placode – Fate-restricted portion of the *cephalic placode whose progenitor cells will produce the crystalline lens of the eye. Optic tract – Large bundle of crossed and uncrossed retinal afferent fibers. In the human brain the majority of the fibers terminate in the *lateral geniculate body; others proceed to the *superior colliculus and some other diencephalic and mesencephalic structures. Optic vesicle – Early diversifying component of the *prosencephalon that will become the source of the *retinal NEP, the *retinal pigment epithelium, and the neuroglia of the *optic nerve and the *optic chiasm. This part of the prosencephalon is already evaginated before closure of the *anterior neuropore. Orbitofrontal NEP – Putative source of neurons and glia of the orbitofrontal cortex. Otic placode – Fate-restricted segregated portion of the *cephalic placode located above the hyoid arch; it begins to evaginate prior to neural tube closure and is nearly completely invaginated by GW3.2. Otic vesicle – The fully invaginated and fused *otic placode that is no longer attached to the head surface and is surrounded by the primordium of the petrous temporal bone. The otic epithelium is the source of neurons in the vestibular and spiral ganglia (*vestibulocochlear ganglion), the cochlea, the semicircular canals, the utricule, and the saccule. Its epithelium touches the brain surface at rhombomere 5.
517 *subventricular zone and the parahippocampal *stratified transitional field.
Parietal lobe or cortex (embryonic) – Region of the developing neocortex bounded anteriorly by the *paracentral lobule and posteriorly by the *occipital lobe. Parietal NEP – Long stretch of the cortical neuroepithelium containing the neural progenitor cells of the *parietal lobe. It is flanked by the parietal *subventricular zone and *stratified transitional field. Perifascicular GEP – Fate-restricted glioepithelium, the presumed source of oligodendrocytes that surround a fiber tract, such as the *fornical GEP. Pineal gland – Midline endocrine gland connected by its stalk to the pineal recess of the dorsal *diencephalic superventricle. It secretes melatonin and other indoleamines. It is believed to receive indirect visual input from the retina. Pituitary gland – See Anterior pituitary gland; Posterior pituitary gland. Pituitary placode – Fate-restricted portion of the *cephalic placode whose progenitor cells form Rathke’s pouch that later becomes the *anterior pituitary gland. The pituitary placode may exert inductive influence on the *hypothalamic NEP to form the *posterior pituitary gland and to generate neurons that produce releasing factors and neurohormones. Placode – See Preplacode. Pons (embryonic) – Developing brainstem region, situated between the *isthmus and the *medulla, that surrounds the anteroventral part of the *rhombencephalic superventricle. It contains some early ascending, descending, and decussating fiber tracts, the sensory and motor nuclei of some of the cranial nerves, and the *reticular formation.
Paracentral NEP – Putative neuroepithelium of the paracentral lobule (pre- and postcentral gyri) in the developing neocortex. It is flanked by the paracentral *subventricular zone and the distinctive paracentral *stratified transitional field.
Pontine gray (embryonic) – This massive basal region of the *pons is just beginning to form during the late first trimester as neurons of the *anterior extramural migratory stream start to settle and the earliest descending *corticofugal fibers reach the site. Corticofugal axons that collateralize here are the principal afferents of the pontine gray neurons that are, in turn, the source of the pontocerebellar fibers of the *middle cerebellar peduncle.
Parahippocampal NEP – Putative source of the neurons and neuroglia of the subicular complex and the entorhinal cortex. It is flanked by the parahippocampal
Posterior commissure (embryonic) – Early-forming decussating fiber tract that interconnects some early generated nuclei of the pretectum.
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GLOSSARY Posterior extramural migratory stream – Subpial stream of young neurons that originate in the *precerebellar NEP. These neurons cross the midline ventrally, and settle on the opposite side to form two precerebellar nuclei contralaterally, the external cuneate nucleus and the lateral reticular nucleus. Posterior intramural migratory stream – Stream of young neurons generated in the *precerebellar NEP that migrate inside the parenchyma to form the *inferior olive in the ventral medulla. Posterior pituitary gland – The posterior lobe of the pituitary gland, also known as the neurohypophysis, is an evagination of the *hypothalamic NEP into posterior Rathke’s pouch. Presumably, it is a glioepithelium that generates the highly specialized pituicytes that surround the axons of the paraventricular and supraoptic nuclei that are the source of oxytocin and vasopressin. Precerebellar NEP – Dorsally situated neuroepithelium that lines the *rhombencephalic superventrticle in the vicinity of the lower rhombic lip and is the source of neurons of the *precerebellar nuclei. Neurons of its rostral division migrate in the *anterior extramural migratory stream and settle in the *pontine gray and the *reticular tegmental nucleus. Neurons of its posterior division form two migratory streams, the *posterior intramural migratory stream that forms the *inferior olive, and the *posterior extramural migratory stream that crosses to the opposite side and forms the *lateral reticular nucleus and the *external cuneate nucleus. Preoptic area (embryonic) – Early developing region surrounding the preoptic recess of the *diencephalic superventricle. It is contiguous anteriorly with the basal telencephalon and blends posteriorly with the anterior *hypothalamus. It is implicated in the regulation of sexual behavior and other reproductive functions. Preplacode – Unique peripheral germinal matrix on the surface of the head and neck that is closely associated with the *neural plate and *neural tube. It is composed of pluripotent – neurogenic and non-neurogenic – progenitor cells that generate diverse specialized components of the head. Its two distinct derivatives are the *cephalic placodes and the *branchial placodes. Pretectal NEP – Germinal matrix anterior to the tectal NEP, the source of pretectal neurons that are the source of the early sprouting fibers of the posterior commissure.
Primary olfactory cortex – That part of the cerebral cortex that gets direct input from the olfactory bulb via the lateral olfactory tract. This cortex contains two cellular layers, a thin cell-dense layer II and a thick layer III of medium cell density. Many neurons appear to migrate into this part of the cortex from the *lateral migratory stream. Primordial plexiform layer – The cell-sparse layer beneath the pia in the early developing *cerebral cortex. This is the first cortical layer to develop and contains the earliest generated *Cajal-Retzius cells, the subplate neurons, and some pioneer cortical afferent axons. A portion of this layer persists as layer I of the mature cortex. Prosencephalon – Primordial vesicle of the forebrain that becomes divided into the paired lateral *telencephalon surrounding the telencephalic superventricles and the medial *diencephalon surrounding the diencephalic superventricle. Purkinje cells (embryonic) – These neurons, which form a monolayer in the maturing cerebellar cortex, are generated in the *cerebellar NEP toward the end of the first trimester, after the production of the *cerebellar deep nuclear neurons. Hence, they are initially situated in the *cortical transition zone (cerebellar transitional field 6), adjacent to the cerebellar NEP, beneath the layers of deep neurons. Later they migrate toward the surface of the formative cerebellar cortex to settle beneath the *external germinal layer. R Rathke’s pouch – The infolding *pituitary placode that, after fusion, forms the *anterior pituitary gland. Red nucleus (embryonic) – A prominent nucleus in the maturing brain with a small-celled (parvocellular) and a large-celled (magnocellular) component. It is recognizable during the first trimester in the vicinity of the putative *rubral NEP. Reticular formation – A large collection of early-developing neurons, enmeshed in a complex network of fibers in the core of the *medulla, the *pons, and the *mesencephalon. Reticular tegmental nucleus (embryonic) – Situated dorsal to the *pontine gray, this precerebellar nucleus, also known as the nucleus reticularis tegmenti pontis, begins to form toward the end of the first trimester before the pontine gray forms. Reticular nucleus (thalamus, embryonic) – An earlyforming, thin belt of cells and fibers between the
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parenchyma of the thalamus and the *internal capsule. Virtually all thalamocortical fibers traverse the thalamic reticular nucleus.
the *subventricular zone of the cerebral cortex to the olfactory bulb. It is a source of late-generated olfactory granule cells and it persists through adulthood.
Retinal NEP – Component of the *optic vesicle germinal matrix that will generate the neurons of the retina.
Rubral NEP – A distinctive neuroepithelial patch lining the *mesencephalic superventricle, situated between the *tectal NEP and the *tegmental NEP. It is the putative source of neurons of the early generated neurons of the *red nucleus.
Retinal pigment epithelium – Component of the *optic vesicle germinal matrix that will generate the nonneural pigment epithelium of the eye. Rhombencephalic superventricle – The greatly expanded NEP-lined lumen of the embryonic *rhombencephalon, situated between the *isthmal canal rostrally and the *central canal caudally, and covered dorsally by the *medullary velum. Among NEP divisions lining the rhombencephalic superventricles are the *cerebellar NEP, the *precerebellar NEP, and the *rhombomere NEPs. The shrunken rhombencephalic superventricle becomes the enduring, *ependyma-lined fourth ventricle. Rhombencephalon (embryonic) – An extremely heterogeneous hindbrain region lining the *rhombencephalic superventricle, that includes the developing cerebellum, pons, and medulla. Rhombic lip, lower – NEP matrix that forms the posterior bridgehead of the medullary velum covering the *rhombencephalic superventricle. It is the source of precerebellar neurons that migrate in the *posterior intramural migratory stream and the *posterior extramural migratory stream. Rhombic lip, upper – NEP matrix that forms the anterior bridgehead of the medullary velum covering the *rhombencephalic superventricle. It is a component of the cerebellar NEP. Following the formation of the *external germinal layer by the end of the first trimester, it is identified as the *germinal trigone of the cerebellum. Rhombomeric NEPs – Prominent neuroepithelial evaginations (bulges) that line the lateral *rhombencephalic superventricle and are morphogenetically related to the *branchial arches and the *branchial placodes. Traditionally, the rhombomeres are distinguished by numbers, as R1 to R7. However, only R2 to R7 have shared characteristics; others identify R1 as the *cerebellar NEP which is very different from the other rhombomeres. We propose the following rhombomeric classification: R2-trigeminal NEP; R3-facial NEP; R4+R5-auditory-vestibular NEP; R6-glossopharyngeal NEP; and R7-vagal NEP. Rostral migratory stream – A large stream of mitotic and postmitotic cells in the forebrain extending from
S Secondary germinal matrix – Layer or field of proliferative progenitors of neurons and neuroglia generated by the receding primary *neuroepithelium. Examples of secondary germinal matrices are the *external germinal layer of the cerebellum, the *subgranular zone of the hippocampal dentate gyrus, and the *subventricular zone of the cerebral cortex and the striatum. Typically, the secondary germinal matrices are the source of late-generated *microneurons. Septal NEP – Midline telencephalic neuroepithelium that produces the neurons and neuroglia of the septal nuclei and Broca’s area. Sojourn zones – Transient cellular layers formed by young neurons that halt their migration for varying periods before they proceed to their final destination. Prominent sojourn zones are present in the *stratified transitional field of the cerebral cortex and in the *cerebellar transitional field. It is hypothesized that the sojourn zones are transient sites where connections are established between translocating neurons and ingrowing fiber tracts, as the first step in the formation of the gross circuitry of the CNS. Stockbuilding NEP –Very few or no differentiating (postmitotic) cells surround the NEP matrix for some time during the early phase of its expansion. The absence of accumulating parenchymal cells indicates that during this period the sole function of NEP cell proliferation is the building of the stock of progenitor cells. Stockbuilding proliferation is referred to as symmetric cell division. This is followed by the asymmetric division of NEP cells, when one daughter cell exits the NEP matrix and starts to differentiate. Stratified transitional field (STF) – As the *cortical plate begins to form, the field situated between it and the NEP matrix becomes stratified. This transient stratified field initially consists of a cell-dense (“cellular”) and a cell-sparse (“fibrous”) layer, STF5 and STF1, respectively. As development proceeds, several other layers emerge (STF2, STF3, STF4, STF6), with pronounced variations in their cellular and fiber composition in motor and sensory regions of the neocortex.
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GLOSSARY Invading *thalamocortical fibers mingle with *corticofugal fibers and with sojourning and migrating neurons in the STF to set up local and extracortical circuitry. A unique feature of the future sensory areas is the *honeycomb matrix. We hypothesize that the STF is a site where unspecified young neurons become specified and where the establishment of interconnections among them commences. This area is also known as the *intermediate zone in some cortical developmental studies. Striatal NEP – Primary germinal source of neurons of the caudate nucleus, putamen, and globus pallidus. It has a large anterolateral and anteromedial division, also known as the lateral and medial eminences, and a small posterior division that generates the neurons of the tail of the caudate nucleus. The posterior striatal NEP is continuous with the *amygdaloid NEP. Striatal subventricular zone (SVZ) – A massive *secondary germinal matrix beneath the striatal NEP. It generates the bulk of the neurons of the *striatum. It may also be the source of some cortical neurons. Striatum – Large component of the *basal ganglia in the ventral telencephalon, consisting of the caudate nucleus, the putamen, and the pallidum (globus pallidus). Strionuclear GEP – Fate-restricted glioepithelium, the putative source of the neuroglia of the stria terminalis, stria medullaris, and possibly other nearby fiber tracts. Strionuclear NEP – Putative neuroepithelial source of the neurons of the bed nucleus of the stria terminalis. It is situated beneath the *striatal NEP in a notch near the *foramen of Monro. Subgranular zone (hippocampus) – *Secondary germinal matrix beneath the granular layer of the hippocampal *dentate gyrus, the source of late generated dentate granule cells. It is recognizable in incipient form by the end of the first trimester and persists into adulthood. Subpial granular layer – Transient cellular layer between the pia and cortical layer I in some regions of the developing *cerebral cortex. It may be a source of cortical astrocytes. Substantia nigra (embryonic) – An early-generated pigmented region in the *tegmentum abutting the future cerebral peduncle. It has two components, the dopaminergic pars compacta and the GABAergic pars reticulata.
Subthalamic NEP – Neuroepithelial division between the *thalamic NEP and the *hypothalamic NEP that generates neurons in Forel’s fields and the zona incerta. Subthalamus (embryonic) – Diencephalic region situated between the *thalamus dorsally and the *hypothalamus ventrally. Its major components, the *zona incerta and Forel’s fields, are recognizable in late first trimester fetuses. Subthalamic nuclear NEP – See Luysiian NEP Subventricular zone (SVZ) – Secondary germinal matrix, derived from the primary *neuroepithelium. The SVZ flanks the NEP during early development and then abuts the ependyma when the NEP dissolves. The nuclei of proliferative SVZ cells, unlike the nuclei of NEP cells, do not shuttle to the lumen of the ventricle during mitosis. Prominent SVZs in the telencephalon are found in the *cerebral cortex and the *striatum. The cells of the *rostral migratory stream derive from the anterior telencephalic SVZ. Superarachnoid reticulum – Expanding and then shrinking cell-sparse tissue between the early-forming pia and the formative dura. This fluid-filled and spongy meningeal tissue provides expansion space for the developing parenchyma and may contain trophic factors to promote that expansion. Superior colliculus (embryonic) – Anterior component of the *tectum (known in lower vertebrates as the optic lobe) is a direct target of optic nerve fibers. Several waves of migrating cells suggest its imminent lamination by the end of the first trimester. There are indications that the entering optic fibers form a *honeycomb matrix superficially, similar to that found in the occipital lobe. Superventricles – The hypertrophied fluid-filled ventricles of the embryonic and early-fetal brain, the superventricles are lined by the expanding *neuroepithelium. Four large components are distinguished: the *telencephalic, *diencephalic, *mesencephalic, and *rhombencephalic superventricles. The initial expansion of the lumen of the superventricles antedates the “flowering” of the embryonic *choroid plexus. However, the sustained inflation of the telencephalic and rhombencephalic superventricles is correlated with the great expansion of the embryonic choroid plexus at these sites. The expanded shorelines of the superventricles promote *stockbuilding NEP cell division, which is sustained for a long time in the cerebral cortex and the cerebellum of the human brain. The superventricles may contain trophic factors that promote NEP cell division.
GLOSSARY T Tectal NEP – Extensive, smooth-surfaced NEP that lines the dorsal bank of the *mesencephalic superventricle. Its most anterior part generates the neurons and neuroglia of the pretectum, a large central part generates those of the *superior colliculus, and its smaller posterior part generates those of the *inferior colliculus. Tectum (embryonic) – Dorsal region of the *mesencephalon, consisting of the *pretectum, *superior colliculus, and *inferior colliculus. Tegmental NEP – The variegated ventral matrix of the *mesencephalic NEP that contains small NEP patches that produce neurons and neuroglia for various nuclei, such as the *red nucleus, the *oculomotor nucleus, the *substantia nigra, and the ventral tegmental area. Tegmentum (embryonic) – Ventral and ventrolateral region of the *mesencephalon. In addition to several brainstem nuclei, it contains many early-forming ascending, decussating, and descending fiber tracts. Some tegmental nuclei have been implicated in somatomotor and visceromotor functions. The onset of development of some components of the tegmentum precede development of the *tectum. Telencephalic superventricle – The largest component of the *superventricles, the paired telencephalic superventricle begins to expand during the early first trimester and shrinks considerably during the third trimester. It is lined laterally, dorsally, and dorsomedially by the extensive *cortical NEP, and ventromedially and ventrally by the smaller *olfactory, *septal, *striatal, *hippocampal, and *amygdaloid NEPs. A large portion of its lumen is occupied by the fetal telencephalic *choroid plexus. The shrunken telencephalic superventricle becomes transformed into the enduring lateral ventricle line by *ependyma. Telencephalon (embryonic) – Extensive forebrain region consisting of both cortical and nuclear (subcortical) components. Among its cortical components are the *cerebral cortex, the *olfactory bulb, and the *hippocampus. Among its nuclear components are the *striatum, *the nucleus accumbens, and the *septum. Temporal NEP – Putative source of neurons and neuroglia of the future temporal lobe, the lateral and ventral portion of the developing cerebral cortex that will later become separated from much of the cerebral hemisphere by the lateral fissure. The temporal NEP is flanked during fetal development by the *subventricular zone and the *stratified transitional field.
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Thalamic NEP – Large division of the *diencephalic NEP, situated above the *subthalamic NEP. Its mosaic divisions are the putative source of neurons and neuroglia of many thalamic nuclei, including the *reticular, *lateral geniculate, and *medial geniculate nuclei. Thalamocortical fibers (embryonic) – Collective term for the large afferent tracts, including the *visual radiation, that proceed from relay nuclei in the thalamus, by way of the *internal capsule, to the *cerebral cortex. Early thalamocortical fibers reach the base of the developing cerebral cortex by GW8 but may not reach the cortical plate for weeks thereafter. Third ventricle – See Diencephalic superventricle. Transpontine corticofugal tract (embryonic) – Portion of the large descending fiber tract in the maturing brain that traverses the *pontine gray and gives off collaterals there. Pioneering fibers of this tract are present by the end of the first trimester. Trigeminal ganglion – A large clump of peripheral sensory neurons located lateral to the trigeminal NEP in rhombomere 2. It is the source of the sensory axons in nerve V that carry light touch and pressure information from the face and jaw. These neurons are presumably generated by the neural crest and by germinal cells in a branchial placode at the junction of the *maxillary process and the mandibular arch. Trigeminal, motor nucleus (embryonic) – Aggregate of trigeminal somatic motor neurons situated medial to the *trigeminal principal sensory nucleus. It is recognizable in late first trimester embryos. Trigeminal, principal sensory nucleus (embryonic) – The second-order sensory neurons in the trigeminal system located dorsal and lateral to the incoming sensory root of cranial *nerve V. It receives topographic somatosensory input from the face and mouth, and its efferents cross the midline in the pons and proceed to the somatosensory thalamus in close association with the *medial lemniscus. The nucleus is prominent by the late first trimester. Trigeminal, spinal nucleus (embryonic) – A continuation of the *trigeminal principal sensory nucleus that extends caudally through the *medulla to the second cervical level of the *spinal cord. It is prominent by the late first trimester. Trigeminal NEP – See Rhombomeric NEPs Trochlear nucleus – Aggregate of somatic motor neurons located posterior to the *oculomotor nucleus that
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GLOSSARY innervate the superior oblique muscle of the eye by way of cranial *nerve IV.
V Vagal ganglia – Superior and inferior clumps of peripheral sensory neurons located in arch IV and extending posteriorly along rhombomere 7. These ganglia are the source of nerve X sensory axons that enter the brain at rhombomere 7 carrying visceral sensory information. These neurons are presumably generated by cells in the neural crest and by a branchial placode in arch IV.
Visual radiation (embryonic) – Thalamocortical fibers that originate in the *lateral geniculate nucleus and terminate in the striate cortex of the *occipital lobe. The identification of *Meyer’s loop at GW11 suggests that this tract may reach the occipital lobe by the end of the first trimester. W
Vagal NEP – See Rhombomeric NEPs .
White matter – General term for extensive regions in the brain and spinal cord composed of myelinated fiber tracts but few or no neuronal cell bodies. In histological preparations with myelin stains, the white matter appears black. In laminated brain regions, as in the *cerebral cortex, the white matter is called the medullary layer.
Vermis – See Cerebellum (vermis).
Z
Vestibulocochlear ganglion – A large clump of peripheral sensory neurons located adjacent to the otic vesicle that later subdivides into the vestibular ganglion and the spiral ganglion. It is the source of nerve VIII axons that enter the brain at rhombomere 4 carrying vestibular and auditory information. These neurons are presumably generated by cells in the otic vesicle epithelium.
Zona incerta (embryonic) – Region in the *subthalamus with uncertain boundaries with Forel’s fields. It is a prominent area in the late first trimester *diencephalon.