Leibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Medical Faculty Jena, University Hospital Jena (UKJ), Jena, Germany.
Nat Rev Mol Cell Biol. 2018 Sep;19(9):594-610. doi: 10.1038/s41580-018-0020-3.
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 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.
成体组织干细胞在多细胞生物的整个生命周期中,对于组织的维持和再生起着关键作用。在生殖后生命期间,组织内稳态的丧失至少部分是由于干细胞功能的下降引起的,并且与疾病发病率的增加有关。衰老的特征包括分子损伤的积累、质量控制系统的失效、代谢变化和表观基因组稳定性的改变。在这篇综述中,我们讨论了最近的证据,支持这样一个新的概念,即在衰老过程中积累的细胞内在损伤以及衰老干细胞龛和血液中细胞外在变化导致干细胞表观基因组的改变。这些在干细胞中累积的表观遗传改变可能是衰老过程中发育途径失调的原因。反过来,它们可能为具有改变的自我更新和功能的突变体和表观遗传漂移的干细胞赋予选择性优势,从而导致与衰老相关的器官功能障碍和疾病的发展。
Nat Rev Mol Cell Biol. 2018-9
Nat Cell Biol. 2016-7-18
Brief Funct Genomics. 2022-1-25
Mamm Genome. 2016-8
J Cell Mol Med. 2019-6-17
Curr Pharm Des. 2012
Trends Cell Biol. 2019-4-25
Epigenomes. 2025-8-8
Int J Mol Sci. 2025-6-22
Nat Cell Biol. 2025-7-1
Cell Stem Cell. 2025-7-3
Nat Chem Biol. 2025-5-26
Front Cell Dev Biol. 2025-4-23
Cells. 2025-2-10