Enhanced neovasculature formation in ischemic myocardium following delivery of pleiotrophin plasmid in a biopolymer

被引:73
作者
Christman, KL
Fang, QZ
Yee, MS
Johnson, KR
Sievers, RE
Lee, RJ
机构
[1] Univ Calif Berkeley, San Francisco, CA 94143 USA
[2] San Francisco Joint Bioengn Grad Grp, San Francisco, CA 94143 USA
[3] Angiogenix Inc, Burlingame, CA 94010 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
关键词
angiogenesis; fibrin; gene therapy; cardiac tissue engineering;
D O I
10.1016/j.biomaterials.2004.04.025
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Coronary heart disease is currently the leading killer in the western world. Therapeutic angiogenic agents are currently being examined for treatment of this disease. We have recently demonstrated the effective use of Pleiotrophin (PTN) as a therapeutic agent for treatment of ischemic myocardium. We have also shown that injection of the biopolymer fibrin glue preserves left ventricular geometry and prevents a deterioration of cardiac function following myocardial infarction. Due to the low transfection efficiency of naked plasmid injections, we examined the use of PTN plasmid and the biopolymer as a gene-activated matrix in the myocardium. In this study, we demonstrate that delivery of PTN plasmid in fibrin glue increases neovasculature formation compared to injection of the naked plasmid in saline. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1139 / 1144
页数:6
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