Engineering enhancement of endothelial cell retention on arterial substitutes
Engineering enhancement of endothelial cell retention on arterial substitutes
批准号:
0932131
负责人:
Shu Liu
金额:
$29.95万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2013-08-31
中文摘要
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英文摘要
This award is funded under the American Recovery and Reinvestment Act of 2009 (Public Law 111-5)0932131LiuBiomaterial-based arterial reconstruction is an effective approach for the treatment of atherosclerosis, the leading cause of human death. However, biomaterials induce thrombosis and intimal hyperplasia, vascular disorders contributing to the failure of reconstructed arteries. While seeding endothelial cells to arterial substitutes is considered a potential approach for preventing these disorders, endothelial cells often detach from the arterial substitute. Thus, an important issue in arterial reconstruction is to enhance the retention of endothelial cells on arterial substitutes. The objective of the proposed research is to establish a molecular engineering approach to enhance endothelial cell retention, reduce thrombosis and intimal hyperplasia, and improve the performance of arterial substitutes. This investigation is focused on two specific aims: enhance endothelial cell retention on biological matrix scaffold- and polytetrafluoroethylene-based arterial substitutes by siRNA-mediated suppression of adhesion-inhibiting molecules, and test the effectiveness of this approach in a rat model of arterial reconstruction. In addition, we propose to improve education technologies by applying the "lab-lecture integration" concept to biomedical engineering curriculum. The intellectual merit of this research stems from the fact that the proposed work may improve the performance of reconstructed arteries by using novel technologies, providing fundamental information for the development of therapeutic approaches for human arterial disorders. This research will exert broad impacts in the following aspects. First, given the high failure rate of reconstructed arteries, results from this research may potentially benefit a large number of patients. Second, the cross-disciplinary collaboration between investigators in biomedical science and bioengineering will broaden the impact of the proposed research and facilitate engineering-life science integration in research and education. Third, this investigation will provide information for improving bioengineering education technologies by integrating research components and lab experiments into lecture topics, an approach potentially influencing future scientific and non-scientific communities through undergraduate and graduate education.
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