Live imaging of wound angiogenesis reveals macrophage orchestrated vessel sprouting and regression
Diagnostic Imaging
Male
0301 basic medicine
wound
610
Neovascularization, Physiologic
Animals, Genetically Modified
angiogenesis
03 medical and health sciences
neutrophils
angiogenesis, inflammation, macrophages, neutrophils, wound
Human Umbilical Vein Endothelial Cells
Animals
Humans
Cells, Cultured
Zebrafish
Wound Healing
Macrophages
Articles
Fibroblasts
macrophages
3. Good health
Mice, Inbred C57BL
inflammation
Centre for Research in Biosciences
DOI:
10.15252/embj.201797786
Publication Date:
2018-06-04T12:39:58Z
AUTHORS (8)
ABSTRACT
Wound angiogenesis is an integral part of tissue repair and is impaired in many pathologies of healing. Here, we investigate the cellular interactions between innate immune cells and endothelial cells at wounds that drive neoangiogenic sprouting in real time and in vivo Our studies in mouse and zebrafish wounds indicate that macrophages are drawn to wound blood vessels soon after injury and are intimately associated throughout the repair process and that macrophage ablation results in impaired neoangiogenesis. Macrophages also positively influence wound angiogenesis by driving resolution of anti-angiogenic wound neutrophils. Experimental manipulation of the wound environment to specifically alter macrophage activation state dramatically influences subsequent blood vessel sprouting, with premature dampening of tumour necrosis factor-α expression leading to impaired neoangiogenesis. Complementary human tissue culture studies indicate that inflammatory macrophages associate with endothelial cells and are sufficient to drive vessel sprouting via vascular endothelial growth factor signalling. Subsequently, macrophages also play a role in blood vessel regression during the resolution phase of wound repair, and their absence, or shifted activation state, impairs appropriate vessel clearance.
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