Open AccessThis article is
- freely available
Extracellular Matrix Molecules Facilitating Vascular Biointegration
The Heart Research Institute, Eliza Street, Newtown, NSW 2042, Australia
Wyss Institute for Biologically Inspired Engineering at Harvard, Boston, MA 02115, USA
* Author to whom correspondence should be addressed.
Received: 29 June 2012; in revised form: 1 August 2012 / Accepted: 6 August 2012 / Published: 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.
Keywords: vascular; biointegration; tropoelastin; fibrillin-1; perlecan; fibulin-5
Article StatisticsClick here to load and display the download statistics.
Notes: Multiple requests from the same IP address are counted as one view.
Cite This Article
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.
Wise SG, Waterhouse A, Michael P, Ng MK. Extracellular Matrix Molecules Facilitating Vascular Biointegration. Journal of Functional Biomaterials. 2012; 3(3):569-587.
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.