赫斯1
Notch信号通路
神经发生
神经干细胞
生物
Hes3信号轴
细胞生物学
神经球
干细胞
大脑
槽口1
神经科学
祖细胞
成体干细胞
胚胎干细胞
信号转导
中枢神经系统
遗传学
基因
作者
Itaru Imayoshi,Masayuki Sakamoto,Masahiro Yamaguchi,Kensaku Mori,Ryoichiro Kageyama
标识
DOI:10.1523/jneurosci.4987-09.2010
摘要
Activation of Notch signaling induces the expression of transcriptional repressor genes such as Hes1 , leading to repression of proneural gene expression and maintenance of neural stem/progenitor cells. However, a requirement for Notch signaling in the telencephalon was not clear, because in Hes1;Hes3;Hes5 triple-mutant mice, neural stem/progenitor cells are depleted in most regions of the developing CNS, but not in the telencephalon. Here, we investigated a role for Notch signaling in the telencephalon by generating tamoxifen-inducible conditional knock-out mice that lack Rbpj , an intracellular signal mediator of all Notch receptors. When Rbpj was deleted in the embryonic brain, almost all telencephalic neural stem/progenitor cells prematurely differentiated into neurons and were depleted. When Rbpj was deleted in the adult brain, all neural stem cells differentiated into transit-amplifying cells and neurons. As a result, neurogenesis increased transiently, but 3 months later all neural stem cells were depleted and neurogenesis was totally lost. These results indicated an absolute requirement of Notch signaling for the maintenance of neural stem cells and a proper control of neurogenesis in both embryonic and adult brains.
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