PDGFRβ+ cells play a dual role as hematopoietic precursors and niche cells during mouse ontogeny

PDGFRβ+细胞在小鼠个体发育过程中发挥着造血前体细胞和微环境细胞的双重作用。

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作者:Diana Sá da Bandeira,Alastair Morris Kilpatrick,Madalena Marques,Mario Gomez-Salazar,Telma Ventura,Zaniah Nashira Gonzalez,Dorota Stefancova,Fiona Rossi,Matthieu Vermeren,Chris Sebastiaan Vink,Mariana Beltran,Neil Cowan Henderson,Bongnam Jung,Reinier van der Linden,Harmen Jan George van de Werken,Wilfred F J van Ijcken,Christer Betsholtz,Stuart John Forbes,Henar Cuervo,Mihaela Crisan

Abstract

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.

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