| Literature DB >> 26619147 |
Roshana Thambyrajah1, Milena Mazan1,2, Rahima Patel1, Victoria Moignard3, Monika Stefanska1, Elli Marinopoulou1, Yaoyong Li4, Christophe Lancrin1,5, Thomas Clapes6, Tarik Möröy7, Catherine Robin6, Crispin Miller4, Shaun Cowley8, Berthold Göttgens3, Valerie Kouskoff9, Georges Lacaud1.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26619147 DOI: 10.1038/ncb3276
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824