BMP and Hedgehog Regulate Distinct AGM Hematopoietic Stem Cells Ex Vivo

Journal Article (2016)
Author(s)

Mihaela Crisan (The University of Edinburgh, Erasmus MC)

Parham Solaimani Kartalaei (Erasmus MC, The University of Edinburgh)

Alex Neagu (Erasmus MC)

Sofia Karkanpouna (Erasmus MC)

Tomoko Yamada-Inagawa (Erasmus MC)

Caterina Purini (Erasmus MC)

Chris S. Vink (The University of Edinburgh, Erasmus MC)

Reinier Van Der Linden (Erasmus MC)

Wilfred Van Ijcken (Erasmus MC)

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DOI related publication
https://doi.org/10.1016/j.stemcr.2016.01.016 Final published version
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Publication Year
2016
Language
English
Affiliation
External organisation
Issue number
3
Volume number
6
Pages (from-to)
383-395
Downloads counter
259

Abstract

Hematopoietic stem cells (HSC), the self-renewing cells of the adult blood differentiation hierarchy, are generated during embryonic stages. The first HSCs are produced in the aorta-gonad-mesonephros (AGM) region of the embryo through endothelial to a hematopoietic transition. BMP4 and Hedgehog affect their production and expansion, but it is unknown whether they act to affect the same HSCs. In this study using the BRE GFP reporter mouse strain that identifies BMP/Smad-activated cells, we find that the AGM harbors two types of adult-repopulating HSCs upon explant culture: One type is BMP-activated and the other is a non-BMP-activated HSC type that is indirectly controlled by Hedgehog signaling through the VEGF pathway. Transcriptomic analyses demonstrate that the two HSC types express distinct but overlapping genetic programs. These results revealing the bifurcation in HSC types at early embryonic stages in the AGM explant model suggest that their development is dependent upon the signaling molecules in the microenvironment.