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

Extracellular Matrix Molecules Facilitating Vascular Biointegration

Received: 29 June 2012; in revised form: 1 August 2012 / Accepted: 6 August 2012 / Published: 14 August 2012
(This article belongs to the Special Issue Biocompatibility of Biomaterials)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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.
Keywords: vascular; biointegration; tropoelastin; fibrillin-1; perlecan; fibulin-5
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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.

AMA Style

Wise SG, Waterhouse A, Michael P, Ng MK. Extracellular Matrix Molecules Facilitating Vascular Biointegration. Journal of Functional Biomaterials. 2012; 3(3):569-587.

Chicago/Turabian Style

Wise, Steven G.; Waterhouse, Anna; Michael, Praveesuda; Ng, Martin K.C. 2012. "Extracellular Matrix Molecules Facilitating Vascular Biointegration." J. Funct. Biomater. 3, no. 3: 569-587.

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