SOX2
生物
祖细胞
少突胶质细胞
细胞生物学
干细胞
细胞分化
KLF4公司
神经发生
背景(考古学)
再生(生物学)
表型
祖细胞
转录组
神经科学
胚胎干细胞
中枢神经系统
基因表达
遗传学
髓鞘
古生物学
基因
作者
Björn Neumann,Michael Segel,Tanay Ghosh,Chao Zhao,Panagiotis Tourlomousis,Adam M. H. Young,Sarah Förster,Amar Sharma,Civia Z. Chen,Juan F. Cubillos,Khalil S. Rawji,Kevin J. Chalut,Robin J.M. Franklin
出处
期刊:Nature Aging
日期:2021-09-14
卷期号:1 (9): 826-837
被引量:16
标识
DOI:10.1038/s43587-021-00109-4
摘要
Like many adult stem cell populations, the capacity of oligodendrocyte progenitor cells (OPCs) to proliferate and differentiate is substantially impaired with aging. Previous work has shown that tissue-wide transient expression of the pluripotency factors Oct4, Sox2, Klf4 and c-Myc extends lifespan and enhances somatic cell function. Here we show that just one of these factors, c-Myc, is sufficient to determine the age state of OPC: c-Myc expression in aged OPCs drives their functional rejuvenation, while its inhibition in neonatal OPCs induces an aged-like phenotype, as determined by in vitro assays and transcriptome analysis. Increasing c-Myc expression in aged OPCs in vivo restores their proliferation and differentiation capacity, thereby enhancing regeneration in an aged central nervous system environment. Our results directly link Myc to cellular activity and cell age state, with implications for understanding regeneration in the context of aging, and provide important insights into the biology of stem cell aging.
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