Author
Listed:
- Claudia Gerri
(Max Planck Institute for Heart and Lung Research)
- Rubén Marín-Juez
(Max Planck Institute for Heart and Lung Research)
- Michele Marass
(Max Planck Institute for Heart and Lung Research)
- Alora Marks
(Max Planck Institute for Heart and Lung Research)
- Hans-Martin Maischein
(Max Planck Institute for Heart and Lung Research)
- Didier Y R. Stainier
(Max Planck Institute for Heart and Lung Research)
Abstract
Macrophages are known to interact with endothelial cells during developmental and pathological angiogenesis but the molecular mechanisms modulating these interactions remain unclear. Here, we show a role for the Hif-1α transcription factor in this cellular communication. We generated hif-1aa;hif-1ab double mutants in zebrafish, hereafter referred to as hif-1α mutants, and find that they exhibit impaired macrophage mobilization from the aorta-gonad-mesonephros (AGM) region as well as angiogenic defects and defective vascular repair. Importantly, macrophage ablation is sufficient to recapitulate the vascular phenotypes observed in hif-1α mutants, revealing for the first time a macrophage-dependent angiogenic process during development. Further substantiating our observations of vascular repair, we find that most macrophages closely associated with ruptured blood vessels are Tnfα-positive, a key feature of classically activated macrophages. Altogether, our data provide genetic evidence that Hif-1α regulates interactions between macrophages and endothelial cells starting with the mobilization of macrophages from the AGM.
Suggested Citation
Claudia Gerri & Rubén Marín-Juez & Michele Marass & Alora Marks & Hans-Martin Maischein & Didier Y R. Stainier, 2017.
"Hif-1α regulates macrophage-endothelial interactions during blood vessel development in zebrafish,"
Nature Communications, Nature, vol. 8(1), pages 1-14, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15492
DOI: 10.1038/ncomms15492
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