蛋白质稳态
皮肤老化
表观遗传学
端粒
医学
基因组不稳定性
衰老
表型
生物
DNA损伤
生物信息学
神经科学
生理学
遗传学
皮肤病科
基因
DNA
作者
Sheng Jin,Kezhu Li,Xiaonan Zong,Seok Chan Eun,Naoki Morimoto,Shu Guo
标识
DOI:10.14336/ad.2023.0321
摘要
Aging is defined as impaired physiological integrity, decreased function, increased susceptibility to external risk factors and various diseases. Skin, the largest organ in our body, may become more vulnerable to insult as time goes by and behave as aged skin. Here, we systemically reviewed three categories including seven hallmarks of skin aging. These hallmarks including genomic instability and telomere attrition, epigenetic alterations and loss of proteostasis, deregulated nutrient-sensing, mitochondrial damage and dysfunction, cellular senescence, stem cell exhaustion/dysregulation, and altered intercellular communication. These seven hallmarks can generally be divided into three categories including (i) causes of damages as primary hallmarks in skin aging; (ii) responses to damage as antagonistic hallmarks in skin aging; and (iii) culprits of the phenotype as integrative hallmarks in skin aging.
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