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Wip1通过p53依赖的细胞周期调控来调节成体嗅球中新神经细胞的生成。

Wip1 regulates the generation of new neural cells in the adult olfactory bulb through p53-dependent cell cycle control.

作者信息

Zhu Yun-Hua, Zhang Cheng-Wu, Lu Li, Demidov Oleg N, Sun Li, Yang Lan, Bulavin Dmitry V, Xiao Zhi-Cheng

机构信息

Department of Clinical Research, Singapore General Hospital, Singapore.

出版信息

Stem Cells. 2009 Jun;27(6):1433-42. doi: 10.1002/stem.65.

Abstract

Continual generation of new neural cells from adult neural stem/progenitor cells (NPCs) is an important component of life-long brain plasticity. However, the intrinsic regulation of this process remains poorly defined. Here we report that Wip1 phosphatase, previously studied in oncogenesis, functions as a crucial physiological regulator in adult neural cell generation. Wip1 deficiency resulted in a 90% decrease in new cell formation in adult olfactory bulb, accompanied by aberrantly decreased NPC amplification, stem cell frequency, and self-renewal. At a cellular level, Wip1 knockout NPCs exhibit a prolonged cell cycle, an accumulation at G(2) to M phase transition, and enhanced p53 activity. Interestingly, the impaired M-phase entry and NPC amplification of Wip1-null mice can be reversed in Wip1/p53 double-null mice. Importantly, there is no difference in NPC amplification between p53-null and Wip1/p53 double-null mice. Our data demonstrate that Wip1 regulates the generation of new neural cells in adult olfactory bulb specifically through p53-dependent M-phase entry of the NPC cell cycle.

摘要

成年神经干细胞/祖细胞(NPCs)持续产生新的神经细胞是终身脑可塑性的重要组成部分。然而,这一过程的内在调节机制仍不清楚。在此我们报告,先前在肿瘤发生研究中涉及的Wip1磷酸酶在成年神经细胞生成中起关键的生理调节作用。Wip1缺陷导致成年嗅球新细胞形成减少90%,同时NPC扩增、干细胞频率和自我更新异常降低。在细胞水平上,Wip1基因敲除的NPCs表现出细胞周期延长,在G(2)到M期转换时积累,并增强p53活性。有趣的是,Wip1基因敲除小鼠的M期进入受损和NPC扩增在Wip1/p53双基因敲除小鼠中可以逆转。重要的是,p53基因敲除小鼠和Wip1/p53双基因敲除小鼠之间的NPC扩增没有差异。我们的数据表明,Wip1通过NPC细胞周期中依赖p53的M期进入,特异性调节成年嗅球新神经细胞的生成。

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