Institute of Genetics and Plant Experimental Biology, Uzbek Academy of Science Tashkent region, Qibray district, Yuqori-Yuz, 702151, Uzbekistan.
Cytotechnology. 2006 Jun;51(2):89-98. doi: 10.1007/s10616-006-9022-7. Epub 2006 Nov 2.
Insect cell lines have been widely used in recombinant baculovirus expression systems and transient gene expression studies. Critical to these applications have been the transfection of foreign DNA. This has been frequently done using labor intensive and cytotoxic liposome-based transfection reagents. In the current study we have optimized a new kind of polyethylenimine-based DNA transfection reagent on the Spodoptera frugiperda Sf9 insect cell line. A plasmid vector that transiently expresses green fluorescent protein (GFP) was effectively delivered into Sf9 cells. A transfection efficiency of 54% and cell viability of 85-90% were obtained for Sf9 cells. The developed transfection protocol has now been successfully used to transfect eight insect cell lines derived from Bombyx mori, Trichoplusia ni, Helicoverpa zea, Heliothis virescens and S. frugiperda with GFP and GUS with transfection efficiencies of at least 45%. This method provides high heterologous protein expression levels, transfection efficacy and cell viability, and could be used for transient gene expression in other lepidopteran cell lines.
昆虫细胞系已广泛应用于重组杆状病毒表达系统和瞬时基因表达研究。这些应用的关键是外源 DNA 的转染。这通常是通过使用劳动密集型和细胞毒性的脂质体转染试剂来完成的。在本研究中,我们对 Spodoptera frugiperda Sf9 昆虫细胞系上的一种新型聚乙烯亚胺基 DNA 转染试剂进行了优化。一个瞬时表达绿色荧光蛋白 (GFP) 的质粒载体被有效地递送到 Sf9 细胞中。Sf9 细胞的转染效率为 54%,细胞活力为 85-90%。该转染方案现已成功用于转染来自家蚕、棉铃虫、玉米螟、烟青虫和 S. frugiperda 的八种昆虫细胞系,转染 GFP 和 GUS 的效率至少为 45%。该方法提供了高的异源蛋白表达水平、转染效率和细胞活力,可用于其他鳞翅目细胞系的瞬时基因表达。