CRUK Stem Cell Biology Group, Cancer Research UK Manchester Institute, The University of Manchester, Wilmslow Road, Manchester M20 4BX, UK.
Haematological Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Nat Cell Biol. 2016 Jan;18(1):21-32. doi: 10.1038/ncb3276. Epub 2015 Nov 30.
In vertebrates, the first haematopoietic stem cells (HSCs) with multi-lineage and long-term repopulating potential arise in the AGM (aorta-gonad-mesonephros) region. These HSCs are generated from a rare and transient subset of endothelial cells, called haemogenic endothelium (HE), through an endothelial-to-haematopoietic transition (EHT). Here, we establish the absolute requirement of the transcriptional repressors GFI1 and GFI1B (growth factor independence 1 and 1B) in this unique trans-differentiation process. We first demonstrate that Gfi1 expression specifically defines the rare population of HE that generates emerging HSCs. We further establish that in the absence of GFI1 proteins, HSCs and haematopoietic progenitor cells are not produced in the AGM, revealing the critical requirement for GFI1 proteins in intra-embryonic EHT. Finally, we demonstrate that GFI1 proteins recruit the chromatin-modifying protein LSD1, a member of the CoREST repressive complex, to epigenetically silence the endothelial program in HE and allow the emergence of blood cells.
在脊椎动物中,具有多谱系和长期重编程潜力的第一批造血干细胞 (HSCs) 出现在 AGM(主动脉-性腺-中肾)区域。这些 HSCs 由称为造血内皮细胞(HE)的罕见和短暂的内皮细胞亚群产生,通过内皮细胞向造血细胞的过渡(EHT)。在这里,我们确定了转录抑制剂 GFI1 和 GFI1B(生长因子独立性 1 和 1B)在这个独特的转化过程中的绝对要求。我们首先证明 Gfi1 表达特异性地定义了产生新兴 HSCs 的罕见 HE 群体。我们进一步确定,在缺乏 GFI1 蛋白的情况下,AGM 中不会产生 HSCs 和造血祖细胞,这揭示了 GFI1 蛋白在胚胎内 EHT 中的关键需求。最后,我们证明 GFI1 蛋白募集染色质修饰蛋白 LSD1(CoREST 抑制复合物的成员),在 HE 中表观遗传沉默内皮程序,并允许血细胞的出现。