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促进血管生物整合的细胞外基质分子

Extracellular matrix molecules facilitating vascular biointegration.

作者信息

Wise Steven G, Waterhouse Anna, Michael Praveesuda, Ng Martin K C

机构信息

The Heart Research Institute, Eliza Street, Newtown, NSW 2042, Australia.

Wyss Institute for Biologically Inspired Engineering at Harvard, Boston, MA 02115, USA.

出版信息

J Funct Biomater. 2012 Aug 14;3(3):569-87. doi: 10.3390/jfb3030569.

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.

摘要

所有血管植入物,包括支架、心脏瓣膜和移植材料,都表现出不理想的生物相容性,这显著降低了它们的临床疗效。已表明内皮下空间中的一系列生物分子在血栓形成、内皮生长和平滑肌细胞增殖的局部调节中起关键作用,这使得它们成为调节血管装置生物整合的有吸引力的候选者。然而,传统使用的生物材料涂层,如纤连蛋白和层粘连蛋白,只调节这些成分中的一种;增强内皮细胞附着,但也激活血小板并引发血栓形成。本综述研究了一部分已证明具有多方面血管相容性的细胞外基质分子,因此它们是改善血管生物材料生物整合的有前途的候选者。

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