Hanzlíková Martina, Soininen Päivi, Lampela Pasi, Männistö Pekka T, Raasmaja Atso
Division of Pharmacology & Toxicology, Faculty of Pharmacy, University of Helsinki, Finland.
Plasmid. 2009 Jan;61(1):15-21. doi: 10.1016/j.plasmid.2008.08.003. Epub 2008 Oct 5.
Polyethylenimines (PEIs) and cationic liposomes are widely used for nonviral gene delivery. When PEIs have been used alone, the transfection efficiency has been higher for larger or linear than smaller or branched PEIs. We have reported previously that a combination of small PEIs and liposomes results in a potentiation of transfection efficiency in vitro. Here, the role of PEI size and structure in this synergism has been clarified further. Therefore, two structurally different high MW PEIs, i.e. the linear PEI22K and branched PEI25K, were studied in the SMC cells. We found that both linear PEI22K and branched PEI25K resulted in a similar synergism and comparable transfection efficiencies. However, the potentiation for larger PEIs found in the present study was weaker than that for smaller PEIs obtained in our previous studies. In conclusion, our present and previous results demonstrate that the increment of PEI/liposome-mediated gene transfection by different types of PEIs in vitro is a common attribute that is rather associated with their size than the structure. Interestingly, the effect of PEI size seems to be opposite when combined with liposome or given alone, i.e. the small PEIs are more effective when combined and less effective when alone than the larger ones.
聚乙烯亚胺(PEIs)和阳离子脂质体被广泛用于非病毒基因递送。当单独使用PEIs时,较大或线性的PEIs比小的或分支状的PEIs转染效率更高。我们之前报道过,小的PEIs与脂质体联合使用可增强体外转染效率。在此,PEI大小和结构在这种协同作用中的作用得到了进一步阐明。因此,在平滑肌细胞中研究了两种结构不同的高分子量PEIs,即线性PEI22K和分支状PEI25K。我们发现线性PEI22K和分支状PEI25K都产生了相似的协同作用和相当的转染效率。然而,本研究中发现的较大PEIs的增强作用比我们之前研究中获得的较小PEIs的增强作用弱。总之,我们目前和之前的结果表明,不同类型的PEIs在体外增强PEI/脂质体介导的基因转染是一个共同特性,这与其大小而非结构有关。有趣的是,当与脂质体联合使用或单独使用时,PEI大小的影响似乎相反,即小的PEIs联合使用时更有效,单独使用时比大的PEIs效果更差。