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Extracellular Matrix Molecules Facilitating Vascular Biointegration
All vascular implants, including stents, heart valves and graft materials exhibit suboptimal biocompatibility that significantly reduces their clinical efficacy. A range of biomolecules in the subendothelial space have been shown to play critical roles in local regulation of thrombosis, endothelial...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031001/ https://www.ncbi.nlm.nih.gov/pubmed/24955633 http://dx.doi.org/10.3390/jfb3030569 |
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author | Wise, Steven G. Waterhouse, Anna Michael, Praveesuda Ng, Martin K.C. |
author_facet | Wise, Steven G. Waterhouse, Anna Michael, Praveesuda Ng, Martin K.C. |
author_sort | Wise, Steven G. |
collection | PubMed |
description | All vascular implants, including stents, heart valves and graft materials exhibit suboptimal biocompatibility that significantly reduces their clinical efficacy. A range of biomolecules in the subendothelial space have been shown to play critical roles in local regulation of thrombosis, endothelial growth and smooth muscle cell proliferation, making these attractive candidates for modulation of vascular device biointegration. However, classically used biomaterial coatings, such as fibronectin and laminin, modulate only one of these components; enhancing endothelial cell attachment, but also activating platelets and triggering thrombosis. This review examines a subset of extracellular matrix molecules that have demonstrated multi-faceted vascular compatibility and accordingly are promising candidates to improve the biointegration of vascular biomaterials. |
format | Online Article Text |
id | pubmed-4031001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40310012014-06-12 Extracellular Matrix Molecules Facilitating Vascular Biointegration Wise, Steven G. Waterhouse, Anna Michael, Praveesuda Ng, Martin K.C. J Funct Biomater Review All vascular implants, including stents, heart valves and graft materials exhibit suboptimal biocompatibility that significantly reduces their clinical efficacy. A range of biomolecules in the subendothelial space have been shown to play critical roles in local regulation of thrombosis, endothelial growth and smooth muscle cell proliferation, making these attractive candidates for modulation of vascular device biointegration. However, classically used biomaterial coatings, such as fibronectin and laminin, modulate only one of these components; enhancing endothelial cell attachment, but also activating platelets and triggering thrombosis. This review examines a subset of extracellular matrix molecules that have demonstrated multi-faceted vascular compatibility and accordingly are promising candidates to improve the biointegration of vascular biomaterials. MDPI 2012-08-14 /pmc/articles/PMC4031001/ /pubmed/24955633 http://dx.doi.org/10.3390/jfb3030569 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Wise, Steven G. Waterhouse, Anna Michael, Praveesuda Ng, Martin K.C. Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title | Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title_full | Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title_fullStr | Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title_full_unstemmed | Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title_short | Extracellular Matrix Molecules Facilitating Vascular Biointegration |
title_sort | extracellular matrix molecules facilitating vascular biointegration |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031001/ https://www.ncbi.nlm.nih.gov/pubmed/24955633 http://dx.doi.org/10.3390/jfb3030569 |
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