San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel.
Nat Rev Mol Cell Biol. 2021 Feb;22(2):75-95. doi: 10.1038/s41580-020-00314-w. Epub 2020 Dec 16.
Cellular senescence, first described in vitro in 1961, has become a focus for biotech companies that target it to ameliorate a variety of human conditions. Eminently characterized by a permanent proliferation arrest, cellular senescence occurs in response to endogenous and exogenous stresses, including telomere dysfunction, oncogene activation and persistent DNA damage. Cellular senescence can also be a controlled programme occurring in diverse biological processes, including embryonic development. Senescent cell extrinsic activities, broadly related to the activation of a senescence-associated secretory phenotype, amplify the impact of cell-intrinsic proliferative arrest and contribute to impaired tissue regeneration, chronic age-associated diseases and organismal ageing. This Review discusses the mechanisms and modulators of cellular senescence establishment and induction of a senescence-associated secretory phenotype, and provides an overview of cellular senescence as an emerging opportunity to intervene through senolytic and senomorphic therapies in ageing and ageing-associated diseases.
细胞衰老最早于 1961 年在体外被描述,目前已成为生物技术公司的研究重点,旨在改善各种人类疾病。细胞衰老的特征是永久性增殖停滞,它是对端粒功能障碍、致癌基因激活和持续 DNA 损伤等内源性和外源性应激的反应。细胞衰老也可以是一种发生在多种生物学过程中的受控程序,包括胚胎发育。衰老细胞的外在活性,与衰老相关的分泌表型的激活密切相关,放大了细胞内在增殖停滞的影响,并导致组织再生受损、慢性与年龄相关的疾病和机体衰老。本文讨论了细胞衰老的建立和衰老相关分泌表型诱导的机制和调节剂,并概述了细胞衰老作为一种通过衰老和与衰老相关疾病的溶胞和形态形成疗法进行干预的新兴机会。