表观遗传学
间充质干细胞
生物
DNA甲基化
衰老
端粒
组蛋白
小RNA
细胞生物学
干细胞
DNA损伤
神经发生的表观遗传调控
表型
间质细胞
表观基因组
遗传学
癌症研究
DNA
基因表达
基因
组蛋白甲基转移酶
作者
Dimitrios Cakouros,Stan Gronthos
出处
期刊:Bone
[Elsevier BV]
日期:2020-08-01
卷期号:137: 115440-115440
被引量:25
标识
DOI:10.1016/j.bone.2020.115440
摘要
There is mounting evidence in the literature that mesenchymal stromal/stem cell (MSC) like populations derived from different tissues, undergo epigenetic changes during aging, leading to compromised connective tissue integrity and function. This body of work has linked the biological aging of MSC to changes in their epigenetic signatures affecting growth, lifespan, self-renewal and multi-potential, due to deregulation of processes such as cellular senescence, oxidative stress, DNA damage, telomere shortening and DNA damage. This review addresses recent findings examining DNA methylation, histone modifications and miRNA changes in aging MSC populations. Moreover, we explore how epigenetic factors alter cellular pathways and associated biological networks, contributing to the MSC aging phenotype. Finally we discuss the crucial areas requiring a greater understanding of these processes, in order to piece together a global picture of the changing epigenetic landscape in MSC during aging.
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