生物
蛋白质稳态
端粒
表观遗传学
基因组不稳定性
衰老
分区(防火)
端粒酶
炎症
长寿
细胞衰老
加速老化
成功老龄化
自噬
神经科学
细胞生物学
遗传学
免疫学
DNA损伤
老年学
细胞凋亡
表型
酶
可靠性工程
工程类
基因
DNA
医学
生物化学
作者
Carlos López-Otı́n,Marı́a A. Blasco,Linda Partridge,Manuel Serrano,Guido Kroemer
出处
期刊:Cell
[Elsevier]
日期:2023-01-01
卷期号:186 (2): 243-278
被引量:1886
标识
DOI:10.1016/j.cell.2022.11.001
摘要
Summary
Aging is driven by hallmarks fulfilling the following three premises: (1) their age-associated manifestation, (2) the acceleration of aging by experimentally accentuating them, and (3) the opportunity to decelerate, stop, or reverse aging by therapeutic interventions on them. We propose the following twelve hallmarks of aging: genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, disabled macroautophagy, deregulated nutrient-sensing, mitochondrial dysfunction, cellular senescence, stem cell exhaustion, altered intercellular communication, chronic inflammation, and dysbiosis. These hallmarks are interconnected among each other, as well as to the recently proposed hallmarks of health, which include organizational features of spatial compartmentalization, maintenance of homeostasis, and adequate responses to stress.
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