在成人神经发生中起重要作用。

Neurogenesis (Austin, Tex.) Pub Date : 2017-02-07 eCollection Date: 2017-01-01 DOI:10.1080/23262133.2016.1270382
Bensun C Fong, Ruth S Slack
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引用次数: 7

摘要

成人神经发生的基本机制尚不清楚。细胞周期机制的成员在调节成体神经干细胞(NSC)的静止和成体出生的神经元群体的大小方面发挥了关键作用。众所周知,视网膜母细胞瘤蛋白Rb具有独立于其作为肿瘤抑制因子的传统作用的中枢神经系统特异性需求。Vandenbosch等人最近的研究阐明了Rb在成体神经发生、增殖限制以及成体神经元长期存活过程中的不同需求。然而,Rb不再被认为是维持成年NSCs静止的主要细胞周期调节因子。未来的研究必须考虑Rb作为更大的调控效应物网络的一部分,包括Rb家族的其他成员,p107和p130。这将有助于阐明Rb和其他口袋蛋白在成人神经发生中的作用,并确定其在调节神经发生生态位的大小和命运中的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RB: An essential player in adult neurogenesis.

The fundamental mechanisms underlying adult neurogenesis remain to be fully clarified. Members of the cell cycle machinery have demonstrated key roles in regulating adult neural stem cell (NSC) quiescence and the size of the adult-born neuronal population. The retinoblastoma protein, Rb, is known to possess CNS-specific requirements that are independent from its classical role as a tumor suppressor. The recent study by Vandenbosch et al. has clarified distinct requirements for Rb during adult neurogenesis, in the restriction of proliferation, as well as long-term adult-born neuronal survival. However, Rb is no longer believed to be the main cell cycle regulator maintaining the quiescence of adult NSCs. Future studies must consider Rb as part of a larger network of regulatory effectors, including the other members of the Rb family, p107 and p130. This will help elucidate the contribution of Rb and other pocket proteins in the context of adult neurogenesis, and define its crucial role in regulating the size and fate of the neurogenic niche.

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