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细胞休眠可塑性:通过调光开关,静止深入衰老。

Cell dormancy plasticity: quiescence deepens into senescence through a dimmer switch.

机构信息

Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona.

Arizona Cancer Center, University of Arizona, Tucson, Arizona.

出版信息

Physiol Genomics. 2020 Nov 1;52(11):558-562. doi: 10.1152/physiolgenomics.00068.2020. Epub 2020 Sep 28.

Abstract

Both being dormant cellular states, quiescence and senescence are traditionally considered distinct. Quiescence is reversible to proliferation upon growth signals, whereas senescence is irreversible in physiological conditions. Recent findings, however, suggest that quiescence deepening with a decreased proliferative tendency, but not capability, is a common transition path toward senescence in many cell and tissue types. This transition is associated with the continuously increased activation threshold of an RB-E2F-CDK gene network switch.

摘要

静止和衰老都是休眠的细胞状态,传统上被认为是不同的。静止在生长信号作用下可恢复增殖,而衰老在生理条件下是不可逆的。然而,最近的发现表明,在许多细胞和组织类型中,静止状态加深,增殖倾向降低,但增殖能力不变,是向衰老转化的常见途径。这种转变与 RB-E2F-CDK 基因网络开关的激活阈值不断增加有关。

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