Suppr超能文献

哺乳动物神经干细胞的细胞周期调控:在 G1 期设置限速。

Cell cycle control of mammalian neural stem cells: putting a speed limit on G1.

机构信息

Samantha Dickson Brain Cancer Unit, UCL Cancer Institute, 72 Huntley Street, London WC1E 6BT, UK.

出版信息

Trends Cell Biol. 2010 May;20(5):233-43. doi: 10.1016/j.tcb.2010.01.006. Epub 2010 Feb 12.

Abstract

The potential to increase unlimitedly in number and to generate differentiated cell types is a key feature of somatic stem cells. Within the nervous system, cellular and environmental determinants tightly control the expansion and differentiation of neural stem cells. Importantly, a number of studies have indicated that changes in cell cycle length can influence development and physiopathology of the nervous system, and might have played a role during evolution of the mammalian brain. Specifically, it has been suggested that the length of G1 can directly influence the differentiation of neural precursors. This has prompted the proposal of a model to explain how manipulation of G1 length can be used to expand neural stem cells. If validated in non-neural systems, this model might provide the means to control the proliferation vs. differentiation of somatic stem cells, which will represent a significant advance in the field.

摘要

无限增殖和产生分化细胞类型的潜力是体干细胞的关键特征。在神经系统中,细胞和环境决定因素严格控制神经干细胞的扩增和分化。重要的是,许多研究表明,细胞周期长度的变化会影响神经系统的发育和病理生理学,并且在哺乳动物大脑的进化过程中可能发挥了作用。具体而言,有人提出 G1 期的长度可以直接影响神经前体细胞的分化。这促使人们提出了一个模型来解释如何操纵 G1 期长度来扩增神经干细胞。如果在非神经系统中得到验证,该模型可能为控制体干细胞的增殖与分化提供手段,这将是该领域的重大进展。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验