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ARTIFICIAL EXTRACELLULAR MATRIX PROTEINS FOR VASCULAR GR

ARTIFICIAL EXTRACELLULAR MATRIX PROTEINS FOR VASCULAR GR
用于血管 GR 的人工细胞外基质蛋白
批准号:
2897320
负责人:
DAVID A TIRRELL
金额:
$21.73万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-08-01 至 2002-07-31

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中文摘要
翻译
这项工作的长期目标是开发新的基因工程材料,用于血管移植物的制造,其特点是改善长期通畅。该方法基于以下假设:现有的合成血管移植物材料——特别是膨胀聚四氟乙烯(ePTFE)和涤纶——在表面化学或机械性能方面都不是最佳的,ii)合成移植物的愈合机制至少部分由细胞与移植物表面或与沉积在该表面的大分子(包括血浆蛋白或细胞外基质(ECM)蛋白)的相互作用控制,iii)通过为特定的细胞表面受体提供配体,可以获得对移植物表面细胞行为的控制措施,iv) ECM蛋白的工程变体将允许控制移植物的关键机械性能和移植物表面配体的呈现。该项目将包括:i).编码含有特定细胞结合和交联结构域的人造ECM蛋白的人工基因的微生物表达,ii).由这些蛋白质制备的交联膜的制备和力学特性,iii).测定在生理相关剪切应力下培养的内皮细胞表面的粘附性。iv)人工细胞外基质培养内皮细胞单层的行为分析。
英文摘要
The long-term objective of this work is the development of new genetically engineered materials to be used in the fabrication of vascular grafts characterized by improving long-term patency. The approach is predicated on the following hypotheses: i). that existing synthetic vascular graft materials - specifically expanded polytetrafluoroethylene (ePTFE) and Dacron - are not optimal, either in terms of surface chemistry or with respect to mechanical properties, ii). that the mechanisms of healing of synthetic grafts are controlled at least in part by cellular interactions with the graft surface or with macromolecules, including plasma proteins or extracellular matrix (ECM) proteins, deposited on that surface, iii). that a measure of control of cellular behavior at the graft surface can be gained by presentation of ligands for specific cell- surface receptors, and iv). that engineered variants of ECM proteins will allow control, both of the key mechanical properties of the graft, and of the presentation of ligands at the graft surface. The project will include: i). microbial expression of artificial genes encoding artificial ECM proteins that incorporate specific cell-binding and crosslinking domains, ii). fabrication and mechanical characterization of crosslinked films prepared from these proteins, iii). determination of the adhesivity of these surfaces with respect to endothelial cells cultured under physiologically relevant shear stresses, and iv). analysis of the behavior of endothelial cell monolayers cultured on artificial extracellular matrices.
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