The transition from radial glial to intermediate progenitor cell is inhibited by FGF signaling during corticogenesis

N/ACitations
Citations of this article
142Readers
Mendeley users who have this article in their library.

Abstract

During corticogenesis, the balance between the self-renewal of radial glial stem cells and the production of their descendent progenitor cells is essential in generating the correct size and cell composition of the neocortex. How the stem-to-progenitor cell transition is regulated is poorly understood. FGFs are commonly implicated in promoting proliferation of neural precursor cells, but it is unclear how they exert their effects on stem cells, progenitor cells, or both in vivo. Here, three FGF receptor genes are simultaneously deleted during cortical neurogenesis. In these mutants, radial glia are depleted due to an increased transition from an uncommitted state to a more differentiated one, initially causing an increase in progenitors, but ultimately resulting in a smaller cortex. The proliferation rate of progenitors themselves, however, is unchanged. These results indicate that FGFs normally repress the radial glia to progenitor cell transition during corticogenesis. Copyright © 2009 Society for Neuroscience.

Cite

CITATION STYLE

APA

Kang, W., Wong, L. C., Shi, S. H., & Hébert, J. M. (2009). The transition from radial glial to intermediate progenitor cell is inhibited by FGF signaling during corticogenesis. Journal of Neuroscience, 29(46), 14571–14580. https://doi.org/10.1523/JNEUROSCI.3844-09.2009

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free