RUNX1 EXPRESSION IN NG2+ PERIVASCULAR CELLS IS REQUIRED FOR PROPER AORTIC EMBRYONIC HAEMATOPOIETIC ACTIVITY IN VIVO
Author(s): ,
Zaniah N Gonzalez Galofre
Affiliations:
Centre for Cardiovascular Science,The University of Edinburgh,Edinburgh,United Kingdom;MRC Centre for Regenerative Medicine,The University of Edinburgh,Edinburgh,United Kingdom
,
Telma Ventura
Affiliations:
MRC Centre for Regenerative Medicine,The University of Edinburgh,Edinburgh,United Kingdom
Mihaela Crisan
Affiliations:
Centre for Cardiovascular Science,The University of Edinburgh,Edinburgh,United Kingdom;MRC Centre for Regenerative Medicine,The University of Edinburgh,Edinburgh,United Kingdom
EHA Library. Gonzalez Galofre Z. Jun 14, 2019; 266252; PF452
Dr. Zaniah Gonzalez Galofre
Dr. Zaniah Gonzalez Galofre
Contributions
Abstract

Abstract: PF452

Type: Poster Pitch

Presentation during EHA24: On Friday, June 14, 2019 from 17:30 - 19:00

Location: Poster area

Background

Insight into the role of the niche in which the first haematopoietic stem cells (HSCs) emerge in vivo is still lacking. These adult-type HSCs are generated in the ventral wall of the dorsal aorta within the aorta-gonad-mesonephros (AGM) region. In the bone marrow, HSCs are mainly located in close association with blood vessel walls. Cells expressing NG2, a cell surface proteoglycan found in both vasculogenic and angiogenic vasculature, have been shown to support adult HSC maintenance. Whether NG2+ cells also control HSC generation in the mouse embryo is still unknown. NG2 expression in the aortic mural cells starts shortly before HSC generation, and some NG2+ cells also express Runx1, a key haematopoietic transcription factor required for HSC generation.

Aims
To investigate whether NG2+Runx1+cells control embryonic haematopoiesis in vivo.

Methods

Runx1 was deleted in NG2 expressing cells by crossing Runx1fl/fl mice with mice containing a Cre transgene under the NG2 promoter. In vitro and in vivo functional assays were performed in E10 and E11 mouse embryos to assess haematopoietic activity. Three-dimensional (3D) confocal imaging of the intact aorta was further used to confirm our results. To investigate whether NG2+ and NG2+Runx1+ cells are haematopoietic and/or haematopoietic precursors, cell sorting and colony-forming assays were carried out on WT, Runx1 GFP and NG2Cre-TdTomato transgenic mice.

Results

By 3D confocal imaging, we found that intra-aortic haematopoietic clusters are dramatically reduced in number in homozygous KO mouse embryos (NG2Cre:Runx1fl/fl) compared to WT (NG2+:Runx1fl/+) controls. This was further confirmed by functional in vitro and in vivo assays. Both haematopoietic progenitors and haematopoietic stem cell activities are affected in the KO AGM.  Depletion of Runx1 in NG2+ cells drastically impairs all haematopoietic progenitor numbers in the dorsal aorta of both E10.5 and E11 mouse embryos and, in vivo, KO AGM had a reduced capacity of reconstituting adult irradiated recipient mice. NG2+ cells (or NG2+Runx1+) are not haematopoietic nor haematopoietic precursors suggesting that NG2+Runx1+ cells act as a supportive niche for haematopoietic progenitor and stem cell generation at this stage.

 

Conclusion

In conclusion, Runx1 expression in the hematopoietic niche is required prior to HPSC generation in the mouse embryo in vivo. Ongoing experiments aim to test whether this is time- and organ-dependent.

Session topic: 23. Hematopoiesis, stem cells and microenvironment

Keyword(s): Microenvironment

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