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Integrin α4β1–VCAM-1–mediated adhesion between endothelial and mural cells is required for blood vessel maturation
Barbara Garmy-Susini, … , Rosa Hwang, Judy Varner
Barbara Garmy-Susini, … , Rosa Hwang, Judy Varner
Published June 1, 2005
Citation Information: J Clin Invest. 2005;115(6):1542-1551. https://doi.org/10.1172/JCI23445.
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Research Article Angiogenesis

Integrin α4β1–VCAM-1–mediated adhesion between endothelial and mural cells is required for blood vessel maturation

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Abstract

Neovascularization depends on vascular cell proliferation and on the stabilization of vessels by association of vascular smooth muscle–like pericytes with ECs. Here we show that integrin α4β1 (VLA-4) and VCAM-1 promote close intercellular adhesion between ECs and pericytes and that this interaction is required for blood vessel formation. Integrin α4β1 is expressed by proliferating but not quiescent ECs, while its ligand VCAM-1 is expressed by proliferating but not quiescent mural cells. Antagonists of this integrin-ligand pair block the adhesion of mural cells to proliferating endothelia in vitro and in vivo, thereby inducing apoptosis of ECs and pericytes and inhibiting neovascularization. These studies indicate that integrin α4β1 and VCAM-1 facilitate a critical cell-cell adhesion event required for survival of endothelial and mural cells during vascularization.

Authors

Barbara Garmy-Susini, Hui Jin, Yuhong Zhu, Rou-Jia Sung, Rosa Hwang, Judy Varner

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Figure 8

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Antagonists of VCAM-1 inhibit angiogenesis. (A) Angiogenesis was initiat...
Antagonists of VCAM-1 inhibit angiogenesis. (A) Angiogenesis was initiated in nude mice by subcutaneous injection of 400 μl growth factor–reduced Matrigel supplemented with 400 ng/ml of bFGF or VEGF-A containing saline, 200 μg rat anti–murine VCAM-1 (M/K-2), or 200 μg isotype-matched control antibodies (normal rat IgG1). After 5 days, tissues were resected and cryosections were immunostained with rat anti–murine CD31 (red structures indicated by arrowheads). Magnification, ×200. (B) CD31-positive vessels per microscopic field were quantified and graphed. Magnification, ×200. *P = 0.0001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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