衰老
端粒
细胞老化
生物
体细胞
细胞生物学
细胞衰老
DNA损伤
长寿
端粒酶
遗传学
DNA
表型
基因
作者
Utz Herbig,Mark Ferreira,Laura Condel,Dee Carey,John M. Sedivy
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2006-02-03
卷期号:311 (5765): 1257-1257
被引量:1008
标识
DOI:10.1126/science.1122446
摘要
The aging of organisms is characterized by a gradual functional decline of all organ systems. Mammalian somatic cells in culture display a limited proliferative life span, at the end of which they undergo an irreversible cell cycle arrest known as replicative senescence. Whether cellular senescence contributes to organismal aging has been controversial. We investigated telomere dysfunction, a recently discovered biomarker of cellular senescence, and found that the number of senescent fibroblasts increases exponentially in the skin of aging baboons, reaching >15% of all cells in very old individuals. In addition, the same cells contain activated ataxia-telangiectasia mutated kinase and heterochromatinized nuclei, confirming their senescent status.
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