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Notch激活通过p53依赖途径诱导神经祖细胞凋亡。

Notch activation induces apoptosis in neural progenitor cells through a p53-dependent pathway.

作者信息

Yang Xudong, Klein Rüdiger, Tian Xiaolin, Cheng Hui-Teng, Kopan Raphael, Shen Jie

机构信息

Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Dev Biol. 2004 May 1;269(1):81-94. doi: 10.1016/j.ydbio.2004.01.014.

Abstract

Notch signaling is involved in a variety of cell-fate decisions during development. Here we investigate the role of Notch signaling in apoptotic cell death of neural progenitors through the generation and analysis of cell type-specific conditional transgenic and knockout mice. We show that conditional expression of a constitutively active form of Notch1 in early neural progenitor cells, but not postmitotic neurons, selectively induces extensive apoptosis, resulting in a markedly reduced progenitor population. Conversely, attenuation of Notch signaling in Notch1 conditional knockout or Presenilin-1-/- mice results in reduced apoptosis of early neural progenitor cells. Furthermore, Notch activation in neural progenitor cells leads to elevated levels of nuclear p53 and transcriptional upregulation of the target genes Bax and Noxa, and the promotion of apoptotic cell death by Notch activation is completely suppressed by p53 deficiency. Together, these complementary gain-of-function and loss-of-function studies reveal a previously unappreciated role of Notch signaling in the regulation of apoptotic cell death during early mammalian neural development.

摘要

Notch信号通路在发育过程中参与多种细胞命运的决定。在此,我们通过构建和分析细胞类型特异性条件转基因和基因敲除小鼠,研究Notch信号通路在神经祖细胞凋亡性细胞死亡中的作用。我们发现,在早期神经祖细胞而非有丝分裂后神经元中条件性表达组成型激活形式的Notch1,可选择性地诱导广泛凋亡,导致祖细胞数量显著减少。相反,在Notch1条件性敲除或早老素1基因敲除小鼠中,Notch信号通路的减弱导致早期神经祖细胞凋亡减少。此外,神经祖细胞中的Notch激活导致核p53水平升高以及靶基因Bax和Noxa的转录上调,而p53缺陷完全抑制了Notch激活对凋亡性细胞死亡的促进作用。总之,这些互补的功能获得和功能缺失研究揭示了Notch信号通路在早期哺乳动物神经发育过程中对凋亡性细胞死亡调控的一个此前未被认识的作用。

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