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

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 g...

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Veröffentlicht in:Nature communications 2013-07, Vol.4 (1), p.2125-2125, Article 2125
Hauptverfasser: Pilz, Gregor-Alexander, Shitamukai, Atsunori, Reillo, Isabel, Pacary, Emilie, Schwausch, Julia, Stahl, Ronny, Ninkovic, Jovica, Snippert, Hugo J., Clevers, Hans, Godinho, Leanne, Guillemot, Francois, Borrell, Victor, Matsuzaki, Fumio, Götz, Magdalena
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Sprache:eng
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Zusammenfassung: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. Amplification of neural progenitor cells mediates expansion of brain regions. Using imaging of progenitor cell amplification in the mouse ventral forebrain, the authors identify a new progenitor type with high frequency, which they also show to be present in expanded brain regions of other species.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms3125