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PDGFRβ+ cells play a dual role as hematopoietic precursors and niche cells during mouse ontogeny.
來源: | 作者:Diana Sá da Bandeira 1, Alastair Morris Kilpatrick 2, Madalena Marques 2, Mario Gomez-Salazar 2, Telma Ventura 2, Zaniah Nashira Gonzalez 1, Dorota Stefancova 2, Fiona Rossi 2, Matthieu Vermeren 2, Chris Sebastiaan Vink 3, Mariana Beltran 3, Neil Cowan He | 發(fā)布時(shí)間: 2022-08-01 | 417 次瀏覽 | 分享到:

Hematopoietic stem cell (HSC) generation in the aorta-gonad-mesonephros region requires HSC specification signals from the surrounding microenvironment. In zebrafish, PDGF-B/PDGFRβ signaling controls hematopoietic stem/progenitor cell (HSPC) generation and is required in the HSC specification niche. Little is known about murine HSPC specification in vivo and whether PDGF-B/PDGFRβ is involved. Here, we show that PDGFRβ is expressed in distinct perivascular stromal cell layers surrounding the mid-gestation dorsal aorta, and its deletion impairs hematopoiesis. We demonstrate that PDGFRβ+ cells play a dual role in murine hematopoiesis. They act in the aortic niche to support HSPCs, and in addition, PDGFRβ+ embryonic precursors give rise to a subset of HSPCs that persist into adulthood. These findings provide crucial information for the controlled production of HSPCs in vitro.

Keywords: AGM single-cell RNA-sequencing; Bmp4; CP: Developmental biology; CP: Stem cell research; HSPC precursor; MSCs; PDGFRβ; VSMCs; hematopoietic niche; osteogenesis; pericytes.


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