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成体干细胞的静息进入、维持和退出。

Quiescence Entry, Maintenance, and Exit in Adult Stem Cells.

机构信息

Department of Biology, Concordia University, 7141 Sherbrooke Street, West, SP Building, Room 501-13, Montreal, QC H4B 1R6, Canada.

出版信息

Int J Mol Sci. 2019 May 1;20(9):2158. doi: 10.3390/ijms20092158.

Abstract

Cells of unicellular and multicellular eukaryotes can respond to certain environmental cues by arresting the cell cycle and entering a reversible state of quiescence. Quiescent cells do not divide, but can re-enter the cell cycle and resume proliferation if exposed to some signals from the environment. Quiescent cells in mammals and humans include adult stem cells. These cells exhibit improved stress resistance and enhanced survival ability. In response to certain extrinsic signals, adult stem cells can self-renew by dividing asymmetrically. Such asymmetric divisions not only allow the maintenance of a population of quiescent cells, but also yield daughter progenitor cells. A multistep process of the controlled proliferation of these progenitor cells leads to the formation of one or more types of fully differentiated cells. An age-related decline in the ability of adult stem cells to balance quiescence maintenance and regulated proliferation has been implicated in many aging-associated diseases. In this review, we describe many traits shared by different types of quiescent adult stem cells. We discuss how these traits contribute to the quiescence, self-renewal, and proliferation of adult stem cells. We examine the cell-intrinsic mechanisms that allow establishing and sustaining the characteristic traits of adult stem cells, thereby regulating quiescence entry, maintenance, and exit.

摘要

单细胞和多细胞真核细胞的细胞可以通过停止细胞周期并进入可逆的静止状态来响应某些环境线索。静止细胞不分裂,但如果暴露于环境中的某些信号,它们可以重新进入细胞周期并恢复增殖。哺乳动物和人类中的静止细胞包括成体干细胞。这些细胞表现出增强的应激抗性和提高的生存能力。响应某些外在信号,成体干细胞可以通过不对称分裂进行自我更新。这种不对称分裂不仅允许维持静止细胞群体,还产生子代祖细胞。这些祖细胞的受控增殖的多步过程导致一种或多种完全分化细胞的形成。成体干细胞维持静止和调节增殖能力的年龄相关下降与许多与衰老相关的疾病有关。在这篇综述中,我们描述了不同类型的静止成体干细胞所共有的许多特征。我们讨论了这些特征如何有助于成体干细胞的静止、自我更新和增殖。我们研究了允许建立和维持成体干细胞特征的细胞内在机制,从而调节静止进入、维持和退出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dffa/6539837/3b4d055c6262/ijms-20-02158-g001.jpg

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