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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Targeting REDV peptide functionalized polycationic gene carrier for enhancing the transfection and migration capability of human endothelial cells
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Targeting REDV peptide functionalized polycationic gene carrier for enhancing the transfection and migration capability of human endothelial cells

机译:靶向REDV肽功能化的聚阳离子基因载体以增强人内皮细胞的转染和迁移能力

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摘要

Targeting gene engineering should be considered as an effective method for promoting endothelialization of vascular grafts. Herein, we developed a targeting REDV peptide functionalized polycationic gene carrier for carrying the pEGFP-ZNF580 plasmid with the aim of enhancing the transfection and migration capability of human endothelial cells. This polycationic gene carrier with the REDV peptide (mPEG-P(LA-co-CL)-PEI-REDV) was prepared by the conjugation of the Cys-Arg-Glu-Asp-Val-Trp (CREDVW) peptide with the amphiphilic block copolymer methoxy poly(ethylene glycol) ether-poly(L-lactide-co-epsilon-caprolactone)-poly(ethyleneimine) (mPEG-P(LA-co-CL)-PEI). mPEG-P(LA-co-CL)-PEI nanoparticles (NP) and mPEG-P(LA-co-CL)-PEI-REDV nanoparticles (REDV-NP) were formed by the self-assembly of the corresponding polycationic polymers, and then their pEGFP-ZNF580 complexes were prepared via the electrostatic interaction with pEGFP-ZNF580 plasmids, respectively. Gel electrophoresis results show that the targeted REDV-NPs could compress pEGFP-ZNF580 plasmids into stable complexes and protect the plasmids against desoxyribonuclease degradation. MTT assay indicates that these targeted REDV-NP/pEGFP-ZNF580 complexes exhibit better cyto-compatibility than the non-targeted NP/pEGFP-ZNF580 complexes and the control PEI 1800 Da/pEGFP-ZNF580 complexes. In vitro transfection experiments and western blot analysis of EA.hy926 endothelial cells show that the pEGFP-ZNF580 plasmid expression and the relative protein level transfected by targeted REDV-NP/pEGFP-ZNF580 complexes are roughly consistent with that transfected by PEI 25 kDa/pEGFP-ZNF580 complexes. More importantly, the scratch wound assay results demonstrate that the migration capability of EA. hy926 cells has been improved significantly by the expression of the pEGFP-ZNF580 plasmid. Our results indicate that the polycationic polymer with functional REDV peptides can be a potential candidate as a pEGFP-ZNF580 plasmid delivery carrier and may be used in the endothelialization of vascular grafts.
机译:靶向基因工程应被视为促进血管移植物内皮化的有效方法。在本文中,我们开发了一种靶向REDV肽功能化的聚阳离子基因载体,用于携带pEGFP-ZNF580质粒,目的是增强人内皮细胞的转染和迁移能力。通过将Cys-Arg-Glu-Asp-Val-Trp(CREDVW)肽与两亲性嵌段缀合来制备带有REDV肽(mPEG-P(LA-co-CL)-PEI-REDV)的多阳离子基因载体共聚物甲氧基聚(乙二醇)醚-聚(L-丙交酯-ε-己内酯)-聚(乙烯亚胺)(mPEG-P(LA-co-CL)-PEI)。 mPEG-P(LA-co-CL)-PEI纳米颗粒(NP)和mPEG-P(LA-co-CL)-PEI-REDV纳米颗粒(REDV-NP)是通过相应聚阳离子聚合物的自组装形成的,然后分别通过与pEGFP-ZNF580质粒的静电相互作用制备它们的pEGFP-ZNF580复合物。凝胶电泳结果表明,靶向的REDV-NPs可以将pEGFP-ZNF580质粒压缩成稳定的复合物,并保护质粒免受脱氧核糖核酸酶降解。 MTT分析表明,这些靶向REDV-NP / pEGFP-ZNF580复合物表现出比非靶向NP / pEGFP-ZNF580复合物和对照PEI 1800 Da / pEGFP-ZNF580复合物更好的细胞相容性。 EA.hy926内皮细胞的体外转染实验和Western印迹分析表明,靶向REDV-NP / pEGFP-ZNF580复合物转染的pEGFP-ZNF580质粒表达和相对蛋白水平与PEI 25 kDa / pEGFP转染的质粒大致一致-ZNF580复合物。更重要的是,刮擦试验的结果证明了EA的迁移能力。通过pEGFP-ZNF580质粒的表达,hy926细胞得到了显着改善。我们的结果表明,具有功能性REDV肽的聚阳离子聚合物可以作为pEGFP-ZNF580质粒递送载体的潜在候选者,并可以用于血管移植物的内皮化。

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