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Vascular endothelial growth factor can signal through platelet-derived growth factor receptors

Vascular endothelial growth factor (VEGF-A) is a crucial stimulator of vascular cell migration and proliferation. Using bone marrow–derived human adult mesenchymal stem cells (MSCs) that did not express VEGF receptors, we provide evidence that VEGF-A can stimulate platelet-derived growth factor rece...

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Detalles Bibliográficos
Autores principales: Ball, Stephen G., Shuttleworth, C. Adrian, Kielty, Cay M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064818/
https://www.ncbi.nlm.nih.gov/pubmed/17470632
http://dx.doi.org/10.1083/jcb.200608093
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author Ball, Stephen G.
Shuttleworth, C. Adrian
Kielty, Cay M.
author_facet Ball, Stephen G.
Shuttleworth, C. Adrian
Kielty, Cay M.
author_sort Ball, Stephen G.
collection PubMed
description Vascular endothelial growth factor (VEGF-A) is a crucial stimulator of vascular cell migration and proliferation. Using bone marrow–derived human adult mesenchymal stem cells (MSCs) that did not express VEGF receptors, we provide evidence that VEGF-A can stimulate platelet-derived growth factor receptors (PDGFRs), thereby regulating MSC migration and proliferation. VEGF-A binds to both PDGFRα and PDGFRβ and induces tyrosine phosphorylation that, when inhibited, results in attenuation of VEGF-A–induced MSC migration and proliferation. This mechanism was also shown to mediate human dermal fibroblast (HDF) migration. VEGF-A/PDGFR signaling has the potential to regulate vascular cell recruitment and proliferation during tissue regeneration and disease.
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spelling pubmed-20648182007-11-29 Vascular endothelial growth factor can signal through platelet-derived growth factor receptors Ball, Stephen G. Shuttleworth, C. Adrian Kielty, Cay M. J Cell Biol Research Articles Vascular endothelial growth factor (VEGF-A) is a crucial stimulator of vascular cell migration and proliferation. Using bone marrow–derived human adult mesenchymal stem cells (MSCs) that did not express VEGF receptors, we provide evidence that VEGF-A can stimulate platelet-derived growth factor receptors (PDGFRs), thereby regulating MSC migration and proliferation. VEGF-A binds to both PDGFRα and PDGFRβ and induces tyrosine phosphorylation that, when inhibited, results in attenuation of VEGF-A–induced MSC migration and proliferation. This mechanism was also shown to mediate human dermal fibroblast (HDF) migration. VEGF-A/PDGFR signaling has the potential to regulate vascular cell recruitment and proliferation during tissue regeneration and disease. The Rockefeller University Press 2007-05-07 /pmc/articles/PMC2064818/ /pubmed/17470632 http://dx.doi.org/10.1083/jcb.200608093 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Ball, Stephen G.
Shuttleworth, C. Adrian
Kielty, Cay M.
Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title_full Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title_fullStr Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title_full_unstemmed Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title_short Vascular endothelial growth factor can signal through platelet-derived growth factor receptors
title_sort vascular endothelial growth factor can signal through platelet-derived growth factor receptors
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064818/
https://www.ncbi.nlm.nih.gov/pubmed/17470632
http://dx.doi.org/10.1083/jcb.200608093
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