祖细胞
生物
细胞生物学
干细胞
造血
细胞分裂
细胞分化
细胞命运测定
胚胎干细胞
成体干细胞
髓样
诱导多能干细胞
免疫学
细胞
遗传学
基因
转录因子
作者
Tatyana Grinenko,Anne Eugster,Lars Thielecke,Beata Ramazs,A. P. Krueger,Sevina Dietz,Ingmar Glauche,Alexander Gerbaulet,Malte von Bonin,Onur Basak,Hans Clevers,Triantafyllos Chavakis,Ben Wielockx
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2018-01-29
摘要
Summary Hematopoietic stem cells (HSCs) continuously replenish all blood cell types through a series of differentiation steps that involve the generation of lineage-committed progenitors as well as necessary expansion due to repeated cell divisions. However, whether cell division in HSCs precedes differentiation is unclear. To this end, we used an HSC cell tracing approach and Ki67 RFP knock-in mice to assess simultaneously divisional history, cell cycle progression, and differentiation of adult HSCs in vivo . Our results reveal that HSCs are able to differentiate into restricted progenitors, especially common myeloid progenitors, restricted megakaryocyte-erythroid progenitors (PreMEs) and pre-megakaryocyte progenitors (PreMegs), without undergoing cell division and even before entering the S phase of the cell cycle. Additionally, the phenotype of the undivided but differentiated progenitors correlated with expression of lineage-specific genes that manifested as functional differences between HSCs and restricted progenitors. Thus, HSC fate decisions appear to be uncoupled from physical cell division. Our results facilitate a better understanding of the mechanisms that control fate decisions in hematopoietic cells. Our data, together with separate findings from embryonic stem cells, suggest that cell division and fate choice are independent processes in pluripotent and multipotent stem cells.
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