Neurogenic inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Medical Biotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Division of Pharmacology, Department of Basic Sciences, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.
Life Sci. 2018 Mar 15;197:101-108. doi: 10.1016/j.lfs.2018.02.008. Epub 2018 Feb 8.
Gene therapy is a promising strategy for the treatment of various diseases. Polyethylenimine (PEI) has received considerable attention for gene delivery applications due to their appropriate properties. However, their toxicity has raised concerns which cause to be used with cautious. This study aimed to prepare different complexes of PEI/DNA and evaluate their parameters affecting in vitro cytotoxicity. Also, apoptosis rate was measured to determine the mechanism of cell toxicity.
The complexes were prepared through conjugation and characterized using dynamic light scattering, MTT and flow cytometry techniques.
The particles' size was from 81 nm to 2785 nm and was increased in the HBS buffer compared to HBG buffer. In the case of branched PEIs, the size of particles was inversely associated with molecular weight. The cytotoxicity results showed that linear 250 KDa PEI was non-toxic whereas branched PEIs with lower molecular weights showed toxicity effects in a concentration dependent manner. Also, the cytotoxicity effects of branched PEIs were proportional with carrier/plasmid (C/P) ratio and were more for the polyplexes prepared in HBG buffer compared to HBS buffer after 24 h incubation. Flow cytometry results confirmed that apoptosis is the main mechanism of cell toxicity produced by polyplexes.
The results showed the effect of PEI size on its cytotoxicity. Also, the toxicity effects of PEI-derived polyplexes in vivo environment was evaluated.
基因治疗是治疗各种疾病的一种很有前途的策略。聚乙稀亚胺(PEI)由于其适当的性质,在基因传递应用中受到了相当多的关注。然而,其毒性引起了人们的关注,因此使用时需要谨慎。本研究旨在制备不同的 PEI/DNA 复合物,并评价其影响体外细胞毒性的参数。同时,测量细胞凋亡率以确定细胞毒性的机制。
通过缀合制备复合物,并使用动态光散射、MTT 和流式细胞术技术进行表征。
颗粒的大小从 81nm 到 2785nm,在 HBS 缓冲液中比在 HBG 缓冲液中有所增加。对于支化 PEI,颗粒的大小与分子量成反比。细胞毒性结果表明,线性 250kDa PEI 无毒性,而分子量较低的支化 PEI 则以浓度依赖的方式表现出毒性作用。此外,支化 PEI 的细胞毒性作用与载体/质粒(C/P)的比例成正比,在 24 小时孵育后,在 HBG 缓冲液中制备的聚集体比在 HBS 缓冲液中更为明显。流式细胞术结果证实,细胞凋亡是多聚物引起细胞毒性的主要机制。
结果表明了 PEI 大小对其细胞毒性的影响。同时,还评价了体内环境中 PEI 衍生的聚集体的毒性作用。