重编程
生物
细胞命运测定
细胞生物学
表观遗传学
后生
氧化磷酸化
胚胎干细胞
细胞内
细胞分化
厌氧糖酵解
细胞
糖酵解
遗传学
新陈代谢
生物化学
DNA甲基化
基因表达
转录因子
基因
作者
Tim S Cliff,Stephen Dalton
标识
DOI:10.1016/j.gde.2017.06.008
摘要
Cell fate decisions are closely linked to changes in metabolic activity. Over recent years this connection has been implicated in mechanisms underpinning embryonic development, reprogramming and disease pathogenesis. In addition to being important for supporting the energy demands of different cell types, metabolic switching from aerobic glycolysis to oxidative phosphorylation plays a critical role in controlling biosynthetic processes, intracellular redox state, epigenetic status and reactive oxygen species levels. These processes extend beyond ATP synthesis by impacting cell proliferation, differentiation, enzymatic activity, ageing and genomic integrity. This review will focus on how metabolic switching impacts decisions made by multipotent cells and discusses mechanisms by which this occurs.
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