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PMID: 11943818 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Dividing precursor cells of the embryonic cortical ventricular zone have morphological and molecular characteristics of radial glia.

Noctor SC, Flint AC, Weissman TA, Wong WS, Clinton BK, Kriegstein AR

Abstract

The embryonic ventricular zone (VZ) of the cerebral cortex contains migrating neurons, radial glial cells, and a large population of cycling progenitor cells that generate newborn neurons. The latter two cell classes have been assumed for some time to be distinct in both function and anatomy, but the cellular anatomy of the progenitor cell type has remained poorly defined. Several recent reports have raised doubts about the distinction between radial glial and precursor cells by demonstrating that radial glial cells are themselves neuronal progenitor cells (Malatesta et al., 2000; Hartfuss et al., 2001; Miyata et al., 2001; Noctor et al., 2001). This discovery raises the possibility that radial glia and the population of VZ progenitor cells may be one anatomical and functional cell class. Such a hypothesis predicts that throughout neurogenesis almost all mitotically active VZ cells and a substantial percentage of VZ cells overall are radial glia. We have therefore used various anatomical, immunohistochemical, and electrophysiological techniques to test these predictions. Our data demonstrate that the majority of VZ cells, and nearly all mitotically active VZ cells during neurogenesis, both have radial glial morphology and express radial glial markers. In addition, intracellular dye filling of electrophysiologically characterized progenitor cells in the VZ demonstrates that these cells have the morphology of radial glia. Because the vast majority cycling cells in the cortical VZ have characteristics of radial glia, the radial glial precursor cell may be responsible for both the production of newborn neurons and the guidance of daughter neurons to their destinations in the developing cortex.

MeSH Terms
Animals Antigens, Differentiation/biosynthesis Biolistics Cell Differentiation/physiology Cell Division Cerebral Cortex/cytology,embryology Cerebral Ventricles/cytology Fluorescent Dyes Green Fluorescent Proteins Immunohistochemistry In Vitro Techniques Luminescent Proteins/biosynthesis,genetics Microspheres Mitosis Neuroglia/cytology Patch-Clamp Techniques Pyramidal Cells/cytology,metabolism Rats Rats, Sprague-Dawley Retroviridae/genetics S Phase Stem Cells/cytology,metabolism Vimentin/biosynthesis
Chemicals
Antigens, Differentiation Fluorescent Dyes Luminescent Proteins Vimentin Green Fluorescent Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Noctor Stephen C
Department of Neurology, Columbia College of Physicians and Surgeons, New York, New York 10032, USA.
Flint Alexander C
Weissman Tamily A
Wong Winston S
Clinton Brian K
Kriegstein Arnold R
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Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
1529-2401
Published
2002-04-15
Pages
3161-73
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6757532
Subset
IM
Grants
NINDS NIH HHS · R01 NS035710 · United States
NINDS NIH HHS · R37 NS035710 · United States
NINDS NIH HHS · NS35710 · United States
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