Cellular senescence in aging and age-related disease: from mechanisms to therapy

被引:1699
作者
Childs, Bennett G. [1 ]
Durik, Matej [2 ]
Baker, Darren J. [1 ,2 ]
van Deursen, Jan M. [1 ,2 ]
机构
[1] Mayo Clin, Coll Med, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Pediat & Adolescent Med, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
NORMAL HUMAN FIBROBLASTS; SMOOTH-MUSCLE-CELLS; INSULIN-RESISTANCE; DNA-DAMAGE; SECRETORY PHENOTYPE; REPLICATIVE SENESCENCE; CHONDROCYTE SENESCENCE; APOPTOSIS RESISTANCE; BETA-GALACTOSIDASE; ENDOTHELIAL-CELLS;
D O I
10.1038/nm.4000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular senescence, a process that imposes permanent proliferative arrest on cells in response to various stressors, has emerged as a potentially important contributor to aging and age-related disease, and it is an attractive target for therapeutic exploitation. A wealth of information about senescence in cultured cells has been acquired over the past half century; however, senescence in living organisms is poorly understood, largely because of technical limitations relating to the identification and characterization of senescent cells in tissues and organs. Furthermore, newly recognized beneficial signaling functions of senescence suggest that indiscriminately targeting senescent cells or modulating their secretome for anti-aging therapy may have negative consequences. Here we discuss current progress and challenges in understanding the stressors that induce senescence in vivo, the cell types that are prone to senesce, and the autocrine and paracrine properties of senescent cells in the contexts of aging and age-related diseases as well as disease therapy.
引用
收藏
页码:1424 / 1435
页数:12
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