4.8 Article

Emergent mechanical control of vascular morphogenesis

Journal

SCIENCE ADVANCES
Volume 9, Issue 32, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.adg9781

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Vascularization is driven by morphogen signals and mechanical cues that regulate cellular force generation, migration, and shape change. The developing vasculature actively regulates its own mechanical properties to achieve effective vascularization. Tissue stiffness increases during vascular morphogenesis resulting from interactions between endothelial cells, fibroblasts, and ECM, and correlates with enhanced vascular function. Contractile cellular forces, synergizing with ECM mechanical properties and mediated by YAP1, play a key role in emergent tissue stiffening and vascular function. Mouse embryos lacking YAP1 in fibroblasts exhibit reduced tissue stiffness and lethal vascular defects. Translating these findings through biology-inspired vascular tissue engineering approaches will have substantial implications in regenerative medicine.
Vascularization is driven by morphogen signals and mechanical cues that coordinately regulate cellular force generation, migration, and shape change to sculpt the developing vascular network. However, it remains unclear whether developing vasculature actively regulates its own mechanical properties to achieve effective vascularization. We engineered tissue constructs containing endothelial cells and fibroblasts to investigate the mechanics of vascularization. Tissue stiffness increases during vascular morphogenesis resulting from emergent interactions between endothelial cells, fibroblasts, and ECM and correlates with enhanced vascular function. Contractile cellular forces are key to emergent tissue stiffening and synergize with ECM mechanical properties to modulate the mechanics of vascularization. Emergent tissue stiffening and vascular function rely on mechanotransduction signaling within fibroblasts, mediated by YAP1. Mouse embryos lacking YAP1 in fibroblasts exhibit both reduced tissue stiffness and develop lethal vascular defects. Translating our findings through biology-inspired vascular tissue engineering approaches will have substantial implications in regenerative medicine.

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