GSK-3 is a master regulator of neural progenitor homeostasis

被引:314
作者
Kim, Woo-Yang [1 ]
Wang, Xinshuo [1 ]
Wu, Yaohong [1 ]
Doble, Bradley W. [2 ]
Patel, Satish [3 ,4 ]
Woodgett, James R. [3 ,4 ]
Snider, William D. [1 ]
机构
[1] Univ N Carolina, Sch Med, Ctr Neurosci, Chapel Hill, NC 27515 USA
[2] McMaster Univ, McMaster Stem Cell & Canc Res Inst, Hamilton, ON, Canada
[3] Univ Toronto, Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[4] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
CELL SELF-RENEWAL; NERVOUS-SYSTEM; STEM-CELLS; N-MYC; NEUROGENESIS; NOTCH; DIFFERENTIATION; PROLIFERATION; KINASE; PLURIPOTENCY;
D O I
10.1038/nn.2408
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. and. 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.
引用
收藏
页码:1390 / 1397
页数:8
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