Ogris Manfred, Wagner Ernst
Cold Spring Harb Protoc. 2012 Feb 1;2012(2):246-50. doi: 10.1101/pdb.prot067868.
Linear polyethylenimine (LPEI) is an efficient transfection reagent for a broad range of cell lines and primary cells and is also useful for local or systemic gene delivery in vivo. In contrast to many other nonviral transfection methods, LPEI is less dependent on mitosis and also transfects postmitotic cells. Transfections can be performed with a simple protocol, as described here. The presence of serum (up to 10%) during transfection does not markedly decrease transfection efficiency, but it significantly reduces toxicity, especially to primary cells. This is a major advantage compared to most lipidic transfection systems. Toxicity can also be kept to a minimum using low, optimized amounts of the transfection reagent. However, LPEI can be quite toxic when applied at elevated doses in vitro or in vivo. LPEI is a fully synthetic product that can be easily synthesized from rather inexpensive precursors and is suitable for large-scale transfections. This protocol describes the synthesis of LPEI from a precursor polymer and the generation of DNA/LPEI polyplexes. Transfection protocols for cells adherent to tissue culture dishes or grown in suspension are given, as are in vivo applications.
线性聚乙烯亚胺(LPEI)是一种适用于多种细胞系和原代细胞的高效转染试剂,也可用于体内局部或全身基因递送。与许多其他非病毒转染方法不同,LPEI对有丝分裂的依赖性较小,还能转染有丝分裂后的细胞。转染可按照此处所述的简单方案进行。转染过程中血清(高达10%)的存在不会显著降低转染效率,但能显著降低毒性,尤其是对原代细胞的毒性。与大多数脂质转染系统相比,这是一个主要优势。使用低剂量、优化用量的转染试剂也可将毒性降至最低。然而,在体外或体内以高剂量应用时,LPEI可能具有相当大的毒性。LPEI是一种完全合成的产品,可由相当廉价的前体轻松合成,适用于大规模转染。本方案描述了由前体聚合物合成LPEI以及生成DNA/LPEI多聚体的过程。还给出了贴壁于组织培养皿或悬浮生长细胞的转染方案以及体内应用方法。