Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783666300336209920 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7969796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangxiaoli thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT fangfei thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT niyinghao thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT yuhongchi thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT majia thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT dengli thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT lichunli thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT shenyang thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT liuxiaoheng thecombinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT wangxiaoli combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT fangfei combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT niyinghao combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT yuhongchi combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT majia combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT dengli combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT lichunli combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT shenyang combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization AT liuxiaoheng combinedcontributionofvascularendothelialcellmigrationandadhesiontostentreendothelialization |