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4 - Neuronal migration

from Section 1 - Making of the brain

Published online by Cambridge University Press:  01 March 2011

Hugo Lagercrantz
Affiliation:
Karolinska Institutet, Stockholm
M. A. Hanson
Affiliation:
Southampton General Hospital
Laura R. Ment
Affiliation:
Yale University, Connecticut
Donald M. Peebles
Affiliation:
University College London
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Summary

Introduction

During brain development, neocortical neurons derive from the primitive neuroepithelium and migrate to their appropriate position in the cerebral mantle, including the cortical plate (or prospective neocortex). In humans, neurons destined to the neocortex migrate mainly between the twelfth and the twenty-fourth week of gestation. In rodents, this developmental period/ontogenic step occurs roughly between embryonic day 12 (the gestation period is about 20 days in these species) and the first postnatal days. The first postmitotic neurons migrate to form a subpial pre-plate or primitive plexiform zone (for a review, see Marin-Padilla,1998) (Fig. 4.1, p. 56). Subsequently produced neurons, which will form the cortical plate, migrate into the pre-plate and divide it into the superficial molecular layer (synonym layer I, marginal zone containing Cajal-Retzius neurons) and the deep subplate (synonym cortical layer VIb). Schematically, successive waves of migratory neurons pass the subplate neurons and end their migratory pathway below layer I. These migrating neurons form successively the cortical layers VIa, V, IV, II, and II, following the inside-out pattern of cortical ontogenesis discovered by the pioneering autoradiographic study of Angevine and Sidman (1961).

Migration pathways and radial glia

A central hypothesis of current developmental neurobiology (for a review, see Rakic,1988) is that migrating neurons find their way from the germinative zone to the cortical plate by climbing along the radially ascending processes of specialized radial glial cells, a finding reported by Rakic (1971).

Type
Chapter
Information
The Newborn Brain
Neuroscience and Clinical Applications
, pp. 55 - 70
Publisher: Cambridge University Press
Print publication year: 2010

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