Stem Cell Laboratory, UCL Cancer Institute, WC1E 6BT London, UK.
Dev Cell. 2013 Aug 12;26(3):237-49. doi: 10.1016/j.devcel.2013.06.023. Epub 2013 Aug 1.
Hematopoietic stem cells (HSCs) emerge during embryogenesis from hemogenic endothelium, but it remains unclear how the HSC lineage is initially established from mesoderm during ontogeny. In Xenopus, the definitive hemangioblast precursors of the HSC lineage have been identified in dorsal lateral plate (DLP) mesoderm, and a transcriptional gene regulatory network (GRN) controlling hemangioblast programming has been elucidated. Herein, we identify an essential role for microRNAs (miRNAs) in establishing the mesodermal lineage leading to both HSC emergence and vasculogenesis and determine that a single miRNA, miR-142-3p, is primarily responsible for initiation of definitive hemangioblast specification. miR-142-3p forms a double-negative gate unlocking entry into the hemangioblast program, in part by inhibiting TGFβ signaling. Our results table miR-142-3p as a master regulator of HSC lineage specification, sitting at the apex of the hierarchy programming the adult hemangioblast, thus illustrating that miRNAs can act as instructive determinants of cell fate during development.
造血干细胞 (HSCs) 是在胚胎发生过程中从造血内皮细胞中出现的,但造血干细胞谱系如何从个体发生过程中的中胚层最初建立仍不清楚。在非洲爪蟾中,HSC 谱系的明确血岛前体细胞已在背侧侧板(DLP)中胚层中被鉴定出来,并且控制血岛编程的转录基因调控网络(GRN)已经阐明。在这里,我们确定了 microRNAs(miRNAs)在建立中胚层谱系方面的重要作用,该谱系导致 HSC 的出现和血管生成,并确定单个 miRNA,miR-142-3p,主要负责启动明确的血岛特化。miR-142-3p 形成一个双重负门,部分通过抑制 TGFβ 信号通路,打开进入血岛程序的入口。我们的结果表明 miR-142-3p 作为 HSC 谱系特化的主调节因子,位于编程成年血岛的层次结构的顶点,因此表明 miRNAs 可以在发育过程中作为细胞命运的指令性决定因素发挥作用。