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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >cMyb regulates hematopoietic stem/progenitor cell mobilization during zebrafish hematopoiesis.
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cMyb regulates hematopoietic stem/progenitor cell mobilization during zebrafish hematopoiesis.

机译:cMyb调节斑马鱼造血过程中的造血干/祖细胞动员。

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摘要

The establishment of the HSC pool in vertebrates depends not only on the formation and the propagation of these stem cells but also on their proper trafficking among the defined hematopoietic organs. However, the physiologic mechanisms that regulate HSC mobilization remain elusive. Through analysis of the zebrafish cmyb mutant cmyb(hkz3), we show that the suppression of cMyb function abrogates larval and adult hematopoiesis, with concomitant accumulation of hematopoietic stem/progenitor cells (HSPCs) in their birthplace, the ventral wall of the dorsal aorta (VDA). Cell tracking and time-lapse recording reveal that the accumulation of HSPCs in cmyb(hkz3) mutants is caused by the impairment of HSPC egression from the VDA. Further analysis demonstrates that the HSPC migratory defects in cmyb(hkz3) mutants are at least partly because of adversely elevated levels of chemokine stromal cell-derived factor 1a (Sdf1a). Our study reveals that cMyb plays a hitherto unidentified role in dictating physiologic HSPC migration by modulating Sdf1a signaling.
机译:HSC池在脊椎动物中的建立不仅取决于这些干细胞的形成和繁殖,还取决于它们在确定的造血器官之间的适当运输。但是,调节HSC动员的生理机制仍然难以捉摸。通过对斑马鱼cmyb突变体cmyb(hkz3)的分析,我们发现抑制cMyb的功能消除了幼虫和成年造血功能,伴随着造血干/祖细胞(HSPC)在其出生地,背主动脉腹壁( VDA)。细胞跟踪和延时记录揭示了cmyb(hkz3)突变体中HSPC的积累是由VDA的HSPC出口受到损害引起的。进一步的分析表明,cmyb(hkz3)突变体中的HSPC迁移缺陷至少部分是由于趋化因子基质细胞衍生因子1a(Sdf1a)的水平升高所致。我们的研究表明,cMyb通过调节Sdf1a信号传导在指导生理性HSPC迁移中起着迄今未发现的作用。

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