4.6 Article

Coupling cell cycle exit, neuronal differentiation and migration in cortical neurogenesis

期刊

CELL CYCLE
卷 5, 期 20, 页码 2314-2318

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.5.20.3381

关键词

p27(Kip1); radial migration; RhoA; neuronal differentiation; Ngn2

资金

  1. Medical Research Council [MC_U117570528] Funding Source: researchfish
  2. MRC [MC_U117570528] Funding Source: UKRI
  3. Medical Research Council [MC_U117570528] Funding Source: Medline

向作者/读者索取更多资源

The generation of new neurons in the cerebral cortex requires that progenitor cells leave the cell cycle and activate specific programs of differentiation and migration. Genetic studies have identified some of the molecules controlling these cellular events, but how the different aspects of neurogenesis are integrated into a coherent develop mental program remains unclear. One possible mechanism implicates multifunctional proteins that regulate, both cell cycle exit and cell differentiation.(1) A prime example is the cyclin-dependent kinase inhibitor p27(Kip1), which has recently been shown to function beyond cell cycle regulation and promote both neuronal differentiation and migration of newborn cortical neurons, through distinct and separable mechanisms. p27(Kip1) is there fore part of a machinery that couples the multiple events of neurogenesis in the cerebral cortex.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据