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J. Funct. Biomater. 2012, 3(3), 569-587; doi:10.3390/jfb3030569

Extracellular Matrix Molecules Facilitating Vascular Biointegration

1
The Heart Research Institute, Eliza Street, Newtown, NSW 2042, Australia
2
Wyss Institute for Biologically Inspired Engineering at Harvard, Boston, MA 02115, USA
*
Author to whom correspondence should be addressed.
Received: 29 June 2012 / Revised: 1 August 2012 / Accepted: 6 August 2012 / Published: 14 August 2012
(This article belongs to the Special Issue Biocompatibility of Biomaterials)
View Full-Text   |   Download PDF [351 KB, uploaded 14 August 2012]   |  

Abstract

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. View Full-Text
Keywords: vascular; biointegration; tropoelastin; fibrillin-1; perlecan; fibulin-5 vascular; biointegration; tropoelastin; fibrillin-1; perlecan; fibulin-5
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Wise, S.G.; Waterhouse, A.; Michael, P.; Ng, M.K. Extracellular Matrix Molecules Facilitating Vascular Biointegration. J. Funct. Biomater. 2012, 3, 569-587.

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