造血
干细胞
造血干细胞
细胞分裂
调节器
平衡
祖细胞
合成代谢
细胞生物学
生物
细胞
遗传学
生物化学
基因
作者
Dirk Loeffler,Timm Schroeder
出处
期刊:Current Opinion in Hematology
[Ovid Technologies (Wolters Kluwer)]
日期:2021-02-26
卷期号:28 (4): 262-268
被引量:13
标识
DOI:10.1097/moh.0000000000000644
摘要
Purpose of review Hematopoietic stem cells (HSCs) are in an inactive quiescent state for most of their life. To replenish the blood system in homeostasis and after injury, they activate and divide. HSC daughter cells must then decide whether to return to quiescence and metabolic inactivity or to activate further to proliferate and differentiate and replenish lost blood cells. Although the regulation of HSC activation is not well understood, recent discoveries shed new light on involved mechanisms including asymmetric cell division (ACD). Recent findings HSC metabolism has emerged as a regulator of cell fates. Recent evidence suggests that cellular organelles mediating anabolic and catabolic processes can be asymmetrically inherited during HSC divisions. These include autophagosomes, mitophagosomes, and lysosomes, which regulate HSC quiescence. Their asymmetric inheritance has been linked to future metabolic and translational activity in HSC daughters, showing that ACD can regulate the balance between HSC (in)activity. Summary We discuss recent insights and remaining questions in how HSCs balance activation and quiescence, with a focus on ACD.
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