Menegatti Sara, Potts Bethany, Garcia-Alegria Eva, Paredes Roberto, Lie-A-Ling Michael, Lacaud Georges, Kouskoff Valerie
Developmental Hematopoiesis Group, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, United Kingdom.
CytoSeek Ltd., Bristol, United Kingdom.
Front Cell Dev Biol. 2021 Dec 16;9:812639. doi: 10.3389/fcell.2021.812639. eCollection 2021.
The transcription factor RUNX1 is a master regulator of blood cell specification. During embryogenesis, hematopoietic progenitors are initially generated from hemogenic endothelium through an endothelium-to-hematopoietic transition controlled by RUNX1. Several studies have dissected the expression pattern and role of RUNX1 isoforms at the onset of mouse hematopoiesis, however the precise pattern of RUNX1 isoform expression and biological output of RUNX1-expressing cells at the onset of human hematopoiesis is still not fully understood. Here, we investigated these questions using a RUNX1b:VENUS RUNX1c:TOMATO human embryonic stem cell line which allows multi-parameter single cell resolution flow cytometry and isolation of RUNX1b-expressing cells for further analysis. Our data reveal the sequential expression of the two RUNX1 isoforms with RUNX1b expressed first in a subset of endothelial cells and during the endothelial to hematopoietic transition while RUNX1c only becomes expressed in fully specified blood cells. Furthermore, our data show that RUNX1b marks endothelial cells endowed with hemogenic potential and that RUNX1b expression level determines hemogenic competency in a dose-dependent manner. Together our data reveal the dynamic of RUNX1 isoforms expression at the onset of human blood specification and establish RUNX1b isoform as the earliest known marker for hemogenic competency.
转录因子RUNX1是血细胞特化的主要调节因子。在胚胎发生过程中,造血祖细胞最初是通过由RUNX1控制的内皮细胞向造血细胞的转变从造血内皮细胞产生的。多项研究剖析了RUNX1异构体在小鼠造血起始阶段的表达模式和作用,然而,RUNX1异构体在人类造血起始阶段的精确表达模式以及表达RUNX1的细胞的生物学输出仍未完全了解。在这里,我们使用RUNX1b:VENUS RUNX1c:TOMATO人类胚胎干细胞系来研究这些问题,该细胞系允许进行多参数单细胞分辨率流式细胞术,并分离出表达RUNX1b的细胞进行进一步分析。我们的数据揭示了两种RUNX1异构体的顺序表达,其中RUNX1b首先在内皮细胞的一个亚群中表达,并在从内皮细胞向造血细胞的转变过程中表达,而RUNX1c仅在完全特化的血细胞中表达。此外,我们的数据表明,RUNX1b标记具有造血潜能的内皮细胞,并且RUNX1b的表达水平以剂量依赖的方式决定造血能力。我们的数据共同揭示了人类血液特化起始阶段RUNX1异构体表达的动态变化,并确定RUNX1b异构体是已知最早的造血能力标志物。