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Pilz, G.-A. ; Shitamukai, A.* ; Reillo, I.* ; Pacary, E.* ; Schwausch, J. ; Stahl, R.* ; Ninkovic, J. ; Snippert, H.J.* ; Clevers, H.* ; Godinho, L. ; Guillemot, F.* ; Borrell, V.* ; Matsuzaki, F.* ; Götz, M.

Amplification of progenitors in the mammalian telencephalon includes a new radial glial cell type.

Nat. Commun. 4:2125 (2013)
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The mechanisms governing the expansion of neuron number in specific brain regions are still poorly understood. Enlarged neuron numbers in different species are often anticipated by increased numbers of progenitors dividing in the subventricular zone. Here we present live imaging analysis of radial glial cells and their progeny in the ventral telencephalon, the region with the largest subventricular zone in the murine brain during neurogenesis. We observe lineage amplification by a new type of progenitor, including bipolar radial glial cells dividing at subapical positions and generating further proliferating progeny. The frequency of this new type of progenitor is increased not only in larger clones of the mouse lateral ganglionic eminence but also in cerebral cortices of gyrated species, and upon inducing gyrification in the murine cerebral cortex. This implies key roles of this new type of radial glia in ontogeny and phylogeny.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Medial Ganglionic Eminence ; Outer Subventricular Zone ; Neural Stem-cells ; Cerebral-cortex ; Neocortical Interneurons ; Lissencephalic Primate ; Embryonic Neocortex ; Globus-pallidus ; Germinal Zones ; Neurons Arise
Language english
Publication Year 2013
HGF-reported in Year 2013
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Journal Nature Communications
Quellenangaben Volume: 4, Issue: , Pages: , Article Number: 2125 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed
Institute(s) Institute of Stem Cell Research (ISF)
POF-Topic(s) 30204 - Cell Programming and Repair
Research field(s) Stem Cell and Neuroscience
PSP Element(s) G-500800-001
PubMed ID 23839311
DOI 10.1038/ncomms3125
WOS ID WOS:000323715900005
Scopus ID 84880288834
Erfassungsdatum 2013-07-16
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