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GSK-3 is a master regulator of neural progenitor homeostasis.

ABSTRACT: The development of the brain requires the exquisite coordination of progenitor proliferation and differentiation to achieve complex circuit assembly. It has been suggested that glycogen synthase kinase 3 (GSK-3) acts as an integrating molecule for multiple proliferation and differentiation signals because of its essential role in the RTK, Wnt and Shh signaling pathways. We created conditional mutations that deleted both the alpha and beta forms of GSK-3 in mouse neural progenitors. GSK-3 deletion resulted in massive hyperproliferation of neural progenitors along the entire neuraxis. Generation of both intermediate neural progenitors and postmitotic neurons was markedly suppressed. These effects were associated with the dysregulation of beta-catenin, Sonic Hedgehog, Notch and fibroblast growth factor signaling. Our results indicate that GSK-3 signaling is an essential mediator of homeostatic controls that regulate neural progenitors during mammalian brain development.

SUBMITTER: Kim WY

PROVIDER: S-EPMC5328673 | biostudies-literature | 2009 Nov

REPOSITORIES: biostudies-literature

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GSK-3 is a master regulator of neural progenitor homeostasis.

Kim Woo-Yang WY Wang Xinshuo X Wu Yaohong Y Doble Bradley W BW Patel Satish S Woodgett James R JR Snider William D WD

Nature neuroscience 20091004 11

The development of the brain requires the exquisite coordination of progenitor proliferation and differentiation to achieve complex circuit assembly. It has been suggested that glycogen synthase kinase 3 (GSK-3) acts as an integrating molecule for multiple proliferation and differentiation signals because of its essential role in the RTK, Wnt and Shh signaling pathways. We created conditional mutations that deleted both the alpha and beta forms of GSK-3 in mouse neural progenitors. GSK-3 deletio ...[more]

PMID: 19801986

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