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Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells

Vascular endothelial growth factor (VEGF) is a potent agonist of angiogenesis that induces proliferation and differentiation of endothelial progenitor cells (EPCs) after vascular injury. Previous studies have suggested that stromal cell-derived factor 1-alpha (SDF-1α) and VEGF have a synergistic eff...

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Autores principales: Yang, Haiyan, He, Cancan, Bi, Yang, Zhu, Xu, Deng, Dan, Ran, Tingting, Ji, Xiaojuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335858/
https://www.ncbi.nlm.nih.gov/pubmed/35910392
http://dx.doi.org/10.3389/fphar.2022.914347
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author Yang, Haiyan
He, Cancan
Bi, Yang
Zhu, Xu
Deng, Dan
Ran, Tingting
Ji, Xiaojuan
author_facet Yang, Haiyan
He, Cancan
Bi, Yang
Zhu, Xu
Deng, Dan
Ran, Tingting
Ji, Xiaojuan
author_sort Yang, Haiyan
collection PubMed
description Vascular endothelial growth factor (VEGF) is a potent agonist of angiogenesis that induces proliferation and differentiation of endothelial progenitor cells (EPCs) after vascular injury. Previous studies have suggested that stromal cell-derived factor 1-alpha (SDF-1α) and VEGF have a synergistic effect on vascular stenosis. The aim of the present study was to investigate whether VEGF and SDF-1α act synergistically in EPCs and vascular smooth muscle cells (VSMCs). In this study, EPCs were isolated from rat bone marrow and their morphology and function were studied. Subsequently, VEGF was delivered into EPCs using an adenoviral vector. Tube formation, migration, proliferation, and apoptosis of VEGF-overexpressing EPCs was analyzed. Then, EPCs were co-cultured with VSMCs in the presence or absence of SDF-1α, the migration, proliferation, apoptosis, and differentiation capacity of EPCs and VSMCs were analyzed respectively. The isolated EPCs showed typical morphological features, phagocytic capacity, and expressed surface proteins. While stable expression of VEGF remarkably enhanced tube formation, migration, and proliferation capacity of EPCs, apoptosis was decreased. Moreover, the proliferation, migration, and differentiation capacity of EPCs in the co-cultured model was enhanced in the presence of SDF-1α, and apoptosis was decreased. However, these effects were reversed in VSMCs. Therefore, our results showed that VEGF and SDF-1α synergistically increased the migration, differentiation, and proliferation capabilities of EPCs, but not VSMCs. This study suggests a promising strategy to prevent vascular stenosis.
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spelling pubmed-93358582022-07-30 Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells Yang, Haiyan He, Cancan Bi, Yang Zhu, Xu Deng, Dan Ran, Tingting Ji, Xiaojuan Front Pharmacol Pharmacology Vascular endothelial growth factor (VEGF) is a potent agonist of angiogenesis that induces proliferation and differentiation of endothelial progenitor cells (EPCs) after vascular injury. Previous studies have suggested that stromal cell-derived factor 1-alpha (SDF-1α) and VEGF have a synergistic effect on vascular stenosis. The aim of the present study was to investigate whether VEGF and SDF-1α act synergistically in EPCs and vascular smooth muscle cells (VSMCs). In this study, EPCs were isolated from rat bone marrow and their morphology and function were studied. Subsequently, VEGF was delivered into EPCs using an adenoviral vector. Tube formation, migration, proliferation, and apoptosis of VEGF-overexpressing EPCs was analyzed. Then, EPCs were co-cultured with VSMCs in the presence or absence of SDF-1α, the migration, proliferation, apoptosis, and differentiation capacity of EPCs and VSMCs were analyzed respectively. The isolated EPCs showed typical morphological features, phagocytic capacity, and expressed surface proteins. While stable expression of VEGF remarkably enhanced tube formation, migration, and proliferation capacity of EPCs, apoptosis was decreased. Moreover, the proliferation, migration, and differentiation capacity of EPCs in the co-cultured model was enhanced in the presence of SDF-1α, and apoptosis was decreased. However, these effects were reversed in VSMCs. Therefore, our results showed that VEGF and SDF-1α synergistically increased the migration, differentiation, and proliferation capabilities of EPCs, but not VSMCs. This study suggests a promising strategy to prevent vascular stenosis. Frontiers Media S.A. 2022-07-15 /pmc/articles/PMC9335858/ /pubmed/35910392 http://dx.doi.org/10.3389/fphar.2022.914347 Text en Copyright © 2022 Yang, He, Bi, Zhu, Deng, Ran and Ji. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Yang, Haiyan
He, Cancan
Bi, Yang
Zhu, Xu
Deng, Dan
Ran, Tingting
Ji, Xiaojuan
Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title_full Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title_fullStr Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title_full_unstemmed Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title_short Synergistic effect of VEGF and SDF-1α in endothelial progenitor cells and vascular smooth muscle cells
title_sort synergistic effect of vegf and sdf-1α in endothelial progenitor cells and vascular smooth muscle cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335858/
https://www.ncbi.nlm.nih.gov/pubmed/35910392
http://dx.doi.org/10.3389/fphar.2022.914347
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