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A stage-specific cell-manipulation platform for inducing endothelialization on demand

Endothelialization is of great significance for vascular remodeling, as well as for the success of implanted vascular grafts/stents in cardiovascular disease treatment. However, desirable endothelialization on synthetic biomaterials remains greatly challenging owing to extreme difficulty in offering...

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Detalles Bibliográficos
Autores principales: Zhao, Qilong, Wang, Juan, Wang, Yunlong, Cui, Huanqing, Du, Xuemin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289041/
https://www.ncbi.nlm.nih.gov/pubmed/34692082
http://dx.doi.org/10.1093/nsr/nwz188
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author Zhao, Qilong
Wang, Juan
Wang, Yunlong
Cui, Huanqing
Du, Xuemin
author_facet Zhao, Qilong
Wang, Juan
Wang, Yunlong
Cui, Huanqing
Du, Xuemin
author_sort Zhao, Qilong
collection PubMed
description Endothelialization is of great significance for vascular remodeling, as well as for the success of implanted vascular grafts/stents in cardiovascular disease treatment. However, desirable endothelialization on synthetic biomaterials remains greatly challenging owing to extreme difficulty in offering dynamic guidance on endothelial cell (EC) functions resembling the native extracellular matrix-mediated effects. Here, we demonstrate a bilayer platform with near-infrared-triggered transformable topographies, which can alter the geometries and functions of human ECs by tunable topographical cues in a remote-controlled manner, yet cause no damage to the cell viability. The migration and the adhesion/spreading of human ECs are respectively promoted by the temporary anisotropic and permanent isotropic topographies of the platform in turn, which appropriately meet the requirements of stage-specific EC manipulation for endothelialization. In addition to the potential of promoting the development of a new generation of vascular grafts/stents enabling rapid endothelialization, this stage-specific cell-manipulation platform also holds promise in various biomedical fields, since the needs for stepwise control over different cell functions are common in wound healing and various tissue-regeneration processes.
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spelling pubmed-82890412021-10-21 A stage-specific cell-manipulation platform for inducing endothelialization on demand Zhao, Qilong Wang, Juan Wang, Yunlong Cui, Huanqing Du, Xuemin Natl Sci Rev Research Article Endothelialization is of great significance for vascular remodeling, as well as for the success of implanted vascular grafts/stents in cardiovascular disease treatment. However, desirable endothelialization on synthetic biomaterials remains greatly challenging owing to extreme difficulty in offering dynamic guidance on endothelial cell (EC) functions resembling the native extracellular matrix-mediated effects. Here, we demonstrate a bilayer platform with near-infrared-triggered transformable topographies, which can alter the geometries and functions of human ECs by tunable topographical cues in a remote-controlled manner, yet cause no damage to the cell viability. The migration and the adhesion/spreading of human ECs are respectively promoted by the temporary anisotropic and permanent isotropic topographies of the platform in turn, which appropriately meet the requirements of stage-specific EC manipulation for endothelialization. In addition to the potential of promoting the development of a new generation of vascular grafts/stents enabling rapid endothelialization, this stage-specific cell-manipulation platform also holds promise in various biomedical fields, since the needs for stepwise control over different cell functions are common in wound healing and various tissue-regeneration processes. Oxford University Press 2020-03 2019-11-21 /pmc/articles/PMC8289041/ /pubmed/34692082 http://dx.doi.org/10.1093/nsr/nwz188 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Qilong
Wang, Juan
Wang, Yunlong
Cui, Huanqing
Du, Xuemin
A stage-specific cell-manipulation platform for inducing endothelialization on demand
title A stage-specific cell-manipulation platform for inducing endothelialization on demand
title_full A stage-specific cell-manipulation platform for inducing endothelialization on demand
title_fullStr A stage-specific cell-manipulation platform for inducing endothelialization on demand
title_full_unstemmed A stage-specific cell-manipulation platform for inducing endothelialization on demand
title_short A stage-specific cell-manipulation platform for inducing endothelialization on demand
title_sort stage-specific cell-manipulation platform for inducing endothelialization on demand
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289041/
https://www.ncbi.nlm.nih.gov/pubmed/34692082
http://dx.doi.org/10.1093/nsr/nwz188
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