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The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization

Coronary stent placement inevitably causes mechanical damage to the endothelium, leading to endothelial denudation and in-stent restenosis (ISR). Re-endothelialization depends mainly on the migration of vascular endothelial cells (VECs) adjacent to the damaged intima, as well as the mobilization and...

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Autores principales: Wang, Xiaoli, Fang, Fei, Ni, Yinghao, Yu, Hongchi, Ma, Jia, Deng, Li, Li, Chunli, Shen, Yang, Liu, Xiaoheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969796/
https://www.ncbi.nlm.nih.gov/pubmed/33748131
http://dx.doi.org/10.3389/fcell.2021.641382
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author Wang, Xiaoli
Fang, Fei
Ni, Yinghao
Yu, Hongchi
Ma, Jia
Deng, Li
Li, Chunli
Shen, Yang
Liu, Xiaoheng
author_facet Wang, Xiaoli
Fang, Fei
Ni, Yinghao
Yu, Hongchi
Ma, Jia
Deng, Li
Li, Chunli
Shen, Yang
Liu, Xiaoheng
author_sort Wang, Xiaoli
collection PubMed
description Coronary stent placement inevitably causes mechanical damage to the endothelium, leading to endothelial denudation and in-stent restenosis (ISR). Re-endothelialization depends mainly on the migration of vascular endothelial cells (VECs) adjacent to the damaged intima, as well as the mobilization and adhesion of circulating VECs. To evaluate the combined contribution of VEC migration and adhesion to re-endothelialization under flow and the influence of stent, in vitro models were constructed to simulate various endothelial denudation scales (2 mm/5 mm/10 mm) and stent deployment depths (flat/groove/bulge). Our results showed that (1) in 2 mm flat/groove/bulge models, both VEC migration and adhesion combined completed the percentage of endothelial recovery about 27, 16, and 12%, and migration accounted for about 21, 15, and 7%, respectively. It was suggested that the flat and groove models were in favor of VEC migration. (2) With the augmentation of the injury scales (5 and 10 mm), the contribution of circulating VEC adhesion on endothelial repair increased. Taken together, endothelial restoration mainly depended on the migration of adjacent VECs when the injury scale was 2 mm. The adhered cells contributed to re-endothelialization in an injury scale-dependent way. This study is helpful to provide new enlightenment for surface modification of cardiovascular implants.
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spelling pubmed-79697962021-03-19 The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization Wang, Xiaoli Fang, Fei Ni, Yinghao Yu, Hongchi Ma, Jia Deng, Li Li, Chunli Shen, Yang Liu, Xiaoheng Front Cell Dev Biol Cell and Developmental Biology Coronary stent placement inevitably causes mechanical damage to the endothelium, leading to endothelial denudation and in-stent restenosis (ISR). Re-endothelialization depends mainly on the migration of vascular endothelial cells (VECs) adjacent to the damaged intima, as well as the mobilization and adhesion of circulating VECs. To evaluate the combined contribution of VEC migration and adhesion to re-endothelialization under flow and the influence of stent, in vitro models were constructed to simulate various endothelial denudation scales (2 mm/5 mm/10 mm) and stent deployment depths (flat/groove/bulge). Our results showed that (1) in 2 mm flat/groove/bulge models, both VEC migration and adhesion combined completed the percentage of endothelial recovery about 27, 16, and 12%, and migration accounted for about 21, 15, and 7%, respectively. It was suggested that the flat and groove models were in favor of VEC migration. (2) With the augmentation of the injury scales (5 and 10 mm), the contribution of circulating VEC adhesion on endothelial repair increased. Taken together, endothelial restoration mainly depended on the migration of adjacent VECs when the injury scale was 2 mm. The adhered cells contributed to re-endothelialization in an injury scale-dependent way. This study is helpful to provide new enlightenment for surface modification of cardiovascular implants. Frontiers Media S.A. 2021-03-04 /pmc/articles/PMC7969796/ /pubmed/33748131 http://dx.doi.org/10.3389/fcell.2021.641382 Text en Copyright © 2021 Wang, Fang, Ni, Yu, Ma, Deng, Li, Shen and Liu. http://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 Cell and Developmental Biology
Wang, Xiaoli
Fang, Fei
Ni, Yinghao
Yu, Hongchi
Ma, Jia
Deng, Li
Li, Chunli
Shen, Yang
Liu, Xiaoheng
The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title_full The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title_fullStr The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title_full_unstemmed The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title_short The Combined Contribution of Vascular Endothelial Cell Migration and Adhesion to Stent Re-endothelialization
title_sort combined contribution of vascular endothelial cell migration and adhesion to stent re-endothelialization
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969796/
https://www.ncbi.nlm.nih.gov/pubmed/33748131
http://dx.doi.org/10.3389/fcell.2021.641382
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