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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >GFI1 and GFI1B control the loss of endothelial identity of hemogenic endothelium during hematopoietic commitment
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GFI1 and GFI1B control the loss of endothelial identity of hemogenic endothelium during hematopoietic commitment

机译:GFI1和GFI1B控制着造血过程中造血内皮的内皮功能丧失

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Recent studies have established that during embryonic development, hematopoietic progenitors and stem cells are generated from hemogenic endothelium precursors through a process termed endothelial to hematopoietic transition (EHT). The transcription factor RUNX1 is essential for this process, but itsmaindownstreameffectors remain largely unknown. Here, we report the identification of Gfi1 and Gfi1b as direct targets of RUNX1 and critical regulators of EHT. GFI1 and GFI1B are able to trigger, in the absence of RUNX1, the down-regulation of endothelial markers and the formation of round cells, a morphologic change characteristic of EHT. Conversely, blood progenitors in Gfi1- and Gfi1b-deficient embryos maintain the expression of endothelial genes. Moreover, those cells are not released from the yolk sac and disseminated into embryonic tissues. Taken together, our findings demonstrate a critical and specific role of the GFI1 transcription factors in the first steps of the process leading to the generation of hematopoietic progenitors from hemogenic endothelium.
机译:最近的研究已经确定,在胚胎发育过程中,造血祖细胞和干细胞是通过称为内皮到造血转变(EHT)的过程从造血内皮前体产生的。转录因子RUNX1对于此过程至关重要,但其主要下游效应子仍然未知。在这里,我们报告鉴定Gfi1和Gfi1b作为RUNX1的直接目标和EHT的关键监管机构。在没有RUNX1的情况下,GFI1和GFI1B能够触发内皮标志物的下调和圆形细胞的形成,这是EHT的形态变化特征。相反,Gfi1和Gfi1b缺陷型胚胎中的血液祖细胞维持内皮基因的表达。而且,那些细胞不会从卵黄囊中释放出来,并不会传播到胚胎组织中。综上所述,我们的发现证明了GFI1转录因子在导致从造血内皮细胞生成造血祖细胞的过程的第一步中的关键和特定作用。

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