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Emergent mechanical control of vascular morphogenesis

Whisler, Jordan; Shahreza, Somayeh; Schlegelmilch, Karin; Ege, Nil; Javanmardi, Yousef; Malandrino, Andrea; Agrawal, Ayushi; Fantin, Alessandro; Serwinski, Bianca; Azizgolshani, Hesham; Park, Clara; Shone, Victoria; Demuren, Olukunle O.; Del Rosario, Amanda; Butty, Vincent L.; Holroyd, Natalie; Domart, Marie-Charlotte; Hooper, Steven; Szita, Nicolas; Boyer, Laurie A.; Walker-Samuel, Simon; Djordjevic, Boris; Sheridan, Graham K.; Collinson, Lucy; Calvo, Fernando; Ruhrberg, Christiana; Sahai, Erik; Kamm, Roger; Moeendarbary, Emad

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Authors

Jordan Whisler

Somayeh Shahreza

Karin Schlegelmilch

Nil Ege

Yousef Javanmardi

Andrea Malandrino

Ayushi Agrawal

Alessandro Fantin

Bianca Serwinski

Hesham Azizgolshani

Clara Park

Victoria Shone

Olukunle O. Demuren

Amanda Del Rosario

Vincent L. Butty

Natalie Holroyd

Marie-Charlotte Domart

Steven Hooper

Nicolas Szita

Laurie A. Boyer

Simon Walker-Samuel

Boris Djordjevic

Lucy Collinson

Fernando Calvo

Christiana Ruhrberg

Erik Sahai

Roger Kamm

Emad Moeendarbary



Abstract

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.

Journal Article Type Article
Acceptance Date Jul 13, 2023
Publication Date Aug 11, 2023
Deposit Date Jan 31, 2024
Publicly Available Date Jan 31, 2024
Journal Science Advances
Publisher American Association for the Advancement of Science
Peer Reviewed Peer Reviewed
Volume 9
Issue 32
Article Number eadg9781
DOI https://doi.org/10.1126/sciadv.adg9781
Keywords Multidisciplinary
Public URL https://nottingham-repository.worktribe.com/output/24424136
Publisher URL https://www.science.org/doi/10.1126/sciadv.adg9781

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