Xie Hao, Liu Xin, Zhou Qing, Huang Teng, Zhang Lu, Gao Jia, Wang Yuhan, Liu Yanjun, Yan Tong, Zhang Shu, Wang Cong-Yi
1The Center for Biomedical Research, Department of Respiratory and Critical Care Medicine, NHC Key Laboratory of Respiratory Disease, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
2Department of Interventional Radiology, Renmin Hospital of Wuhan University, Wuhan, China.
Aging Dis. 2022 Apr 1;13(2):433-446. doi: 10.14336/AD.2021.0904. eCollection 2022 Apr.
Aging has been recognized to be a highly complex biological health problem with a high risk of chronic diseases, including type 2 diabetes, atherosclerosis, chronic bronchitis or emphysema, cancer and Alzheimer's disease. Particularly, age-related turnover in adipose tissue is a major contributor to metabolic syndromes and shortened lifespan. Adipocytes undergo senescence in early stage, which results in adipose tissue metabolic dysfunction, redistribution, and inflammation. The well-established association between DNA methylation (DNAm) and aging has been observed in the past few decades. Indeed, age-related alteration in DNAm is highly tissue-specific. This review intends to summarize the advancements how DNAm changes coupled with aging process in adipose tissue, by which DNAm regulates cellular senescence, metabolic function, adipokine secretion and beiging process in adipocytes. Elucidation of the effect of DNAm on adipose aging would have great potential to the development of epigenetic therapeutic strategies against aging-related diseases in clinical settings.
衰老已被公认为是一个高度复杂的生物健康问题,患有包括2型糖尿病、动脉粥样硬化、慢性支气管炎或肺气肿、癌症和阿尔茨海默病在内的慢性疾病的风险很高。特别是,脂肪组织中与年龄相关的更新是代谢综合征和寿命缩短的主要原因。脂肪细胞在早期会发生衰老,这会导致脂肪组织代谢功能障碍、重新分布和炎症。在过去几十年中,人们已经观察到DNA甲基化(DNAm)与衰老之间存在着已确立的关联。事实上,DNAm中与年龄相关的变化具有高度的组织特异性。本综述旨在总结DNAm如何随着脂肪组织衰老过程而变化的研究进展,DNAm通过这些变化调节脂肪细胞中的细胞衰老、代谢功能、脂肪因子分泌和米色化过程。阐明DNAm对脂肪衰老的影响对于临床环境中针对衰老相关疾病的表观遗传治疗策略的开发具有巨大潜力。