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Cardiac Usage of Reducible Poly(oligo-D-arginine) As a Gene Carrier for Vascular Endothelial Growth Factor Expression

机译:可还原的聚(寡聚-D-精氨酸)作为血管内皮生长因子表达的基因载体的心脏用途。

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摘要

Developments of non-viral carriers have headed toward reducing cytotoxicity, which results from the use of conventional gene carriers, and enhancing gene delivery efficiency. Cys-(d-R9)-Cys repeated reducible poly(oligo-D-arginine) (rPOA) is one of the most efficient non-viral carriers for gene therapy; however, while its efficiency has been verified in the lung and brain, it is necessary to confirm its activity in each organ or tissue since there are differences of gene carrier susceptibility to among tissue types. We therefore tested the compatibility of rPOA in cardiac tissue by in vitro or in vivo experiments and confirmed its high transfection efficiency and low cytotoxicity. Moreover, substantial regenerative effects were observed following transfection with rPOA/pVEGF expression vector complexes (79% decreased infarct size) compared to polyethyleneimine (PEI) (34% decreased infarct size) in a rat myocardial infarction (MI) model. These findings suggest that rPOA efficiently enables DNA transfection in cardiac tissue and can be used as a useful non-viral therapeutic gene carrier for gene therapy in ischemic heart disease.
机译:非病毒载体的发展已朝着减少由于使用常规基因载体而导致的细胞毒性和提高基因传递效率的方向发展。 Cys-(d-R9)-Cys重复还原型聚(寡聚-D-精氨酸)(rPOA)是基因治疗中最有效的非病毒载体之一;然而,尽管已经在肺和脑中验证了其有效性,但是由于不同组织类型之间基因载体敏感性的差异,因此有必要确认其在每个器官或组织中的活性。因此,我们通过体外或体内实验测试了rPOA在心脏组织中的相容性,并证实了其高转染效率和低细胞毒性。此外,在大鼠心肌梗死(MI)模型中,与聚乙烯亚胺(PEI)(梗死面积减少34%)相比,用rPOA / pVEGF表达载体复合物转染(梗死面积减少了79%)观察到了显着的再生作用。这些发现表明,rPOA有效地使心脏组织中的DNA转染,并可用作缺血性心脏病的基因治疗的有用的非病毒治疗基因载体。

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