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Effects of Lipofectamine 2000/siRNA Complexes on Autophagy in Hepatoma Cells

机译:Lipofectamine 2000 / siRNA复合物对肝癌细胞自噬的影响

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摘要

Lipofectamine 2000 is commonly used for siRNA transfections. However, few studies have examined cellular responses to this delivery system. The purpose of this study is to evaluate the effect of siRNA transfection using Lipofectamine 2000 on cellular autophagy. Huh7.5 cells, stably-transfected to express GFP-LC3, were treated with Lipofectamine 2000egative control siRNA (NC siRNA) complexes. At different time points after treatment, cells were lysed and analyzed by immunoblotting and fluorescence spectroscopy. Cells were also observed using confocal microscopy. An increase of endogenous LC3 lipidation, GFP-LC3 fluorescence, and autophagosomal puncta was observed in cells treated with Lipofectamine 2000/NC siRNA complexes. The kinetics of the increase of GFP-LC3 fluorescence correlated with the concentration of NC siRNA transfected, where 50, 100, and 200 nM NC siRNA caused a significant increase at 72, 48 and 24 hours, respectively, after transfection. A similar effect on the GFP-LC3 signal was also observed for cells treated with Lipofectamine 2000 complexed with two other NC siRNAs. Lipofectamine 2000-mediated transport of NC siRNAs led to an increase of autophagosomes in a dose- and time-dependent manner. Thus, this effect on cells should be taken into consideration when using this approach for intracellular delivery of siRNA.
机译:Lipofectamine 2000通常用于siRNA转染。然而,很少有研究已经检查了对该递送系统的细胞反应。本研究的目的是评估siRNA转染在细胞自噬上的脂质凝乳胺2000的效果。 Huh7.5稳定转染表达GFP-LC3的细胞用Lipofectamine 2000 /阴性对照siRNA(NC siRNA)配合物处理。在处理后的不同时间点,通过免疫印迹和荧光光谱裂解细胞并分析。还使用共聚焦显微镜观察细胞。在用Lipofectamine 2000 / NC siRNA复合物处理的细胞中观察到内源性LC3脂质,GFP-LC3荧光和自噬体斑点的增加。与转染50,100和200nM的NC siRNA浓度相关的GFP-LC3荧光的动力学与转染后分别在72,48和24小时内显着增加。还观察到对用脂质切积胺2000与另外两个NC siRNA络合的细胞对GFP-LC3信号的影响。 Lipofectamine 2000介导的NC siRNA的传输导致剂量和时间依赖性的自噬体增加。因此,在使用这种方法的分细胞分娩时,应考虑对细胞对细胞的这种影响。

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