| Literature DB >> 31685991 |
Rodolphe Gautier1, Laurence Petit1, Laurent Yvernogeau1,2, Hanane Khoury1, Frédéric Relaix3, Vanessa Ribes4, Helen Sang5, Pierre Charbord1, Michèle Souyri1,6, Catherine Robin2,7, Thierry Jaffredo8.
Abstract
It is well established that haematopoietic stem and progenitor cells (HSPCs) are generated from a transient subset of specialized endothelial cells termed haemogenic, present in the yolk sac, placenta and aorta, through an endothelial-to-haematopoietic transition (EHT). HSPC generation via EHT is thought to be restricted to the early stages of development. By using experimental embryology and genetic approaches in birds and mice, respectively, we document here the discovery of a bone marrow haemogenic endothelium in the late fetus/young adult. These cells are capable of de novo producing a cohort of HSPCs in situ that harbour a very specific molecular signature close to that of aortic endothelial cells undergoing EHT or their immediate progenies, i.e., recently emerged HSPCs. Taken together, our results reveal that HSPCs can be generated de novo past embryonic stages. Understanding the molecular events controlling this production will be critical for devising innovative therapies.Entities:
Mesh:
Year: 2019 PMID: 31685991 DOI: 10.1038/s41556-019-0410-6
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824