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Electroporation-mediated delivery of a naked DNA plasmid expressing VEGF to the porcine heart enhances protein expression.

机译:将表达VEGF的裸DNA质粒的递送介导的递送至猪心脏增强了蛋白质表达。

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摘要

Gene therapy is an attractive method for the treatment of cardiovascular disease. However, using current strategies, induction of gene expression at therapeutic levels is often inefficient. In this study, we show a novel electroporation (EP) method to enhance the delivery of a plasmid expressing an angiogenic growth factor (vascular endothelial growth factor, VEGF), which is a molecule previously documented to stimulate revascularization in coronary artery disease. DNA expression plasmids were delivered in vivo to the porcine heart with or without coadministered EP to determine the potential effect of electrically mediated delivery. The results showed that plasmid delivery through EP significantly increased cardiac expression of VEGF compared with injection of plasmid alone. This is the first report showing successful intracardiac delivery, through in vivo EP, of a protein expressing plasmid in a large animal.
机译:基因治疗是一种有吸引力的治疗心血管疾病的方法。 然而,使用当前策略,治疗水平的基因表达诱导往往效率低下。 在该研究中,我们展示了一种新型电穿孔(EP)方法,以增强表达血管生成生长因子(血管内皮生长因子,VEGF)的质粒的递送,这是先前记录刺激冠状动脉疾病中血运重建的分子。 DNA表达质粒在体内递送至猪心脏,或没有共同静电EP以确定电介导的递送的潜在效果。 结果表明,与单独的质粒注射质粒,通过EP的质粒递送显着增加了VEGF的心脏表达。 这是第一份表明在大型动物中表达蛋白质的蛋白质中成功的心内递送的报告。

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