In the spotlight: the role of TGFβ signalling in haematopoietic stem and progenitor cell emergence

被引:3
作者
Thambyrajah, Roshana [1 ]
Monteiro, Rui [2 ,3 ,4 ]
机构
[1] IMIM, Stem Cell & Canc Grp, Barcelona, Spain
[2] Univ Birmingham, Inst Canc & Genom Sci, Coll Med & Dent Sci, Birmingham, W Midlands, England
[3] Univ Birmingham, Birmingham Ctr Genome Biol, Birmingham, W Midlands, England
[4] Canc Res UK Birmingham Ctr, Birmingham, W Midlands, England
关键词
AORTIC ENDOTHELIUM; RUNX1; EXPRESSION; KINASE; SPECIFICATION; PATHWAY; IDENTIFICATION; PROLIFERATION; TRANSITION; MATURATION; EMBRYO;
D O I
10.1042/BST20210363
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Haematopoietic stem and progenitor cells (HSPCs) sustain haematopoiesis by generating precise numbers of mature blood cells throughout the lifetime of an individual. In verte-brates, HSPCs arise during embryonic development from a specialised endothelial cell population, the haemogenic endothelium (HE). Signalling by the Transforming Growth Factor 0 (TGF0) pathway is key to regulate haematopoiesis in the adult bone marrow, but evidence for a role in the formation of HSPCs has only recently started to emerge. In this review, we examine recent work in various model systems that demonstrate a key role for TGF0 signalling in HSPC emergence from the HE. The current evidence underpins two seemingly contradictory views of TGF0 function: as a negative regulator of HSPCs by lim-iting haematopoietic output from HE, and as a positive regulator, by programming the HE towards the haematopoietic fate. Understanding how to modulate the requirement for TGF0 signalling in HSC emergence may have critical implications for the generation of these cells in vitro for therapeutic use.
引用
收藏
页码:703 / 712
页数:10
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