| Literature DB >> 27421959 |
Céline Souilhol1, Javier G Lendinez1, Stanislav Rybtsov1, Fiona Murphy1, Heather Wilson1, David Hills1, Antoniana Batsivari1, Anahí Binagui-Casas1, Alison C McGarvey1, H Robson MacDonald2, Ryoichiro Kageyama3, Christian Siebel4, Suling Zhao1, Alexander Medvinsky1.
Abstract
The first definitive hematopoietic stem cells (dHSCs) in the mouse emerge in the dorsal aorta of the embryonic day (E) 10.5 to 11 aorta-gonad-mesonephros (AGM) region. Notch signaling is essential for early HSC development but is dispensable for the maintenance of adult bone marrow HSCs. How Notch signaling regulates HSC formation in the embryo is poorly understood. We demonstrate here that Notch signaling is active in E10.5 HSC precursors and involves both Notch1 and Notch2 receptors, but is gradually downregulated while they progress toward dHSCs at E11.5. This downregulation is accompanied by gradual functional loss of Notch dependency. Thus, as early as at final steps in the AGM region, HSCs begin acquiring the Notch independency characteristic of adult bone marrow HSCs as part of the maturation program. Our data indicate that fine stage-dependent tuning of Notch signaling may be required for the generation of definitive HSCs from pluripotent cells.Entities:
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Year: 2016 PMID: 27421959 PMCID: PMC5034738 DOI: 10.1182/blood-2016-03-708164
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476