Cellular and epigenetic drivers of stem cell ageing

被引:181
作者
Ermolaeva, Maria [1 ]
Neri, Francesco [1 ]
Ori, Alessandro [1 ]
Rudolph, K. Lenhard [1 ,2 ]
机构
[1] FLI, Leibniz Inst Aging, Jena, Germany
[2] Univ Hosp Jena UKJ, Med Fac Jena, Jena, Germany
基金
欧洲研究理事会;
关键词
MITOCHONDRIAL-DNA MUTATIONS; INTESTINAL-STEM; SKELETAL-MUSCLE; LIFE-SPAN; CLONAL HEMATOPOIESIS; PROGENITOR CELLS; SELF-RENEWAL; DIETARY RESTRICTION; GENE-EXPRESSION; P38; MAPK;
D O I
10.1038/s41580-018-0020-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adult tissue stem cells have a pivotal role in tissue maintenance and regeneration throughout the lifespan of multicellular organisms. Loss of tissue homeostasis during post-reproductive reproductive lifespan is caused, at least in part, by a decline in stem cell function and is associated with an increased incidence of diseases. Hallmarks of ageing include the accumulation of molecular damage, failure of quality control systems, metabolic changes and alterations in epigenome stability. In this Review, we discuss recent evidence in support of a novel concept whereby cell-intrinsic damage that accumulates during ageing and cell-extrinsic changes in ageing stem cell niches and the blood result in modifications of the stem cell epigenome. These cumulative epigenetic alterations in stem cells might be the cause of the deregulation of developmental pathways seen during ageing. In turn, they could confer a selective advantage to mutant and epigenetically drifted stem cells with altered self-renewal and functions, which contribute to the development of ageing-associated organ dysfunction and disease.
引用
收藏
页码:594 / 610
页数:17
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