Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.

OBJECTIVES: Recent findings suggest that in response to repair-to-injury bone marrow mesenchymal stem cells (BMSCs) participate in the process of angiogenesis. It is unclear what role BMSCs play in the structure of the vessel wall. In present study, we aimed to determine whether BMSCs had the capaci...

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Main Authors: Mincai Li, Suqin Li, Liangzhu Yu, Jiliang Wu, Tonghui She, Yaping Gan, Zhenwu Hu, Wenli Liao, Hongli Xia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3857273?pdf=render
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spelling doaj-75065a44a627492ebfac803cd1ccde0c2020-11-24T21:54:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8274310.1371/journal.pone.0082743Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.Mincai LiSuqin LiLiangzhu YuJiliang WuTonghui SheYaping GanZhenwu HuWenli LiaoHongli XiaOBJECTIVES: Recent findings suggest that in response to repair-to-injury bone marrow mesenchymal stem cells (BMSCs) participate in the process of angiogenesis. It is unclear what role BMSCs play in the structure of the vessel wall. In present study, we aimed to determine whether BMSCs had the capacity of endothelial cells (ECs). METHODS: BMSCs were separated and cultured. FACS and RT-PCR analysis confirmed the gene expression phenotype. The capacity of migration and adhesion and the ultrastructure of BMSCs were examined. The effect of BMSCs transplantation on the vascular repair was investigated in a murine carotid artery-injured model. RESULTS: BMSCs could express some markers and form the tube-like structure. The migration and adhesion capacity of BMSCs increased significantly after stimulated. In addition, BMSCs had the intact cell junction. In vivo the local transfer of BMSCs differentiated into neo-endothelial cells in the injury model for carotid artery and contributed to the vascular remodeling. CONCLUSION: These results showed that BMSCs could contribute to neointimal formation for vascular lesion and might be associated with the differentiation into ECs, which indicated the important therapeutic implications for vascular diseases.http://europepmc.org/articles/PMC3857273?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mincai Li
Suqin Li
Liangzhu Yu
Jiliang Wu
Tonghui She
Yaping Gan
Zhenwu Hu
Wenli Liao
Hongli Xia
spellingShingle Mincai Li
Suqin Li
Liangzhu Yu
Jiliang Wu
Tonghui She
Yaping Gan
Zhenwu Hu
Wenli Liao
Hongli Xia
Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
PLoS ONE
author_facet Mincai Li
Suqin Li
Liangzhu Yu
Jiliang Wu
Tonghui She
Yaping Gan
Zhenwu Hu
Wenli Liao
Hongli Xia
author_sort Mincai Li
title Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
title_short Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
title_full Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
title_fullStr Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
title_full_unstemmed Bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
title_sort bone mesenchymal stem cells contributed to the neointimal formation after arterial injury.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description OBJECTIVES: Recent findings suggest that in response to repair-to-injury bone marrow mesenchymal stem cells (BMSCs) participate in the process of angiogenesis. It is unclear what role BMSCs play in the structure of the vessel wall. In present study, we aimed to determine whether BMSCs had the capacity of endothelial cells (ECs). METHODS: BMSCs were separated and cultured. FACS and RT-PCR analysis confirmed the gene expression phenotype. The capacity of migration and adhesion and the ultrastructure of BMSCs were examined. The effect of BMSCs transplantation on the vascular repair was investigated in a murine carotid artery-injured model. RESULTS: BMSCs could express some markers and form the tube-like structure. The migration and adhesion capacity of BMSCs increased significantly after stimulated. In addition, BMSCs had the intact cell junction. In vivo the local transfer of BMSCs differentiated into neo-endothelial cells in the injury model for carotid artery and contributed to the vascular remodeling. CONCLUSION: These results showed that BMSCs could contribute to neointimal formation for vascular lesion and might be associated with the differentiation into ECs, which indicated the important therapeutic implications for vascular diseases.
url http://europepmc.org/articles/PMC3857273?pdf=render
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