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PMID: 3152420 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Redistribution of synaptic vesicle antigens is correlated with the disappearance of a transient synaptic zone in the developing cerebral cortex.

Neuron ·Vol. 1 ·No. 4 ·1988-06-00 ·Pages 297-310

Chun JJ, Shatz CJ

Abstract

To examine the distribution of synaptic vesicle antigens during development of the cerebral cortex, antibodies against synapsin I and p65 were used on sections of cat cerebral cortex between E40 and adulthood. In the adult, the layers of the cerebral cortex are immunoreactive for each of these antigens, while the white matter is free of staining. In contrast, the fetal and neonatal pattern of immunostaining is reversed: the cortical plate (future cortical layers) is devoid of immunoreactivity, while the marginal (future layer 1) and the intermediate zones (future white matter) are stained. Electron microscopic immunohistochemistry shows that immunolabeling is associated with presynaptic nerve terminals in the adult and during development. These observations suggest that during development the white matter is a transient synaptic neuropil and that a global redistribution of synapses takes place as the mature pattern of connections within the cerebral cortex emerges.

MeSH Terms
Aging Animals Antigens/analysis Cats Cerebral Cortex/cytology,embryology,growth & development Embryonic and Fetal Development Immunohistochemistry Membrane Proteins/analysis Nerve Tissue Proteins/analysis Organ Specificity Synapses/physiology,ultrastructure Synapsins Synaptic Vesicles/physiology,ultrastructure
Chemicals
Antigens Membrane Proteins Nerve Tissue Proteins Synapsins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Chun J J
Department of Neurobiology, Stanford University School of Medicine, California 94305.
Shatz C J
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1988-06-00
Pages
297-310
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NIGMS NIH HHS · GM07365 · United States
NEI NIH HHS · K04EY00248 · United States
NEI NIH HHS · R01EY02858 · United States
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