Rheiner Steven, Reichel Derek, Rychahou Piotr, Izumi Tadahide, Yang Hsin-Sheng, Bae Younsoo
Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone, Lexington, KY 40536, USA.
Markey Cancer Center, University of Kentucky, 800 Rose Street, CC140, Lexington, KY 40536, USA; Department of Surgery, College of Medicine, University of Kentucky, 741 South Limestone, Lexington, KY 40536, USA.
Int J Pharm. 2017 Aug 7;528(1-2):536-546. doi: 10.1016/j.ijpharm.2017.06.056. Epub 2017 Jun 16.
Poly(ethylene glycol)-conjugated polyethylenimine (PEG-PEI) is a widely studied cationic polymer used to develop non-viral vectors for siRNA therapy of genetic disorders including cancer. Cell lines stably expressing luciferase reporter protein typically evaluate the transfection efficacy of siRNA/PEG-PEI complexes, however recent findings revealed that PEG-PEI can reduce luciferase expression independent of siRNA. This study elucidates a cause of the false positive effect in luciferase assays by using polymer nanoassemblies (PNAs) made from PEG, PEI, poly-(l-lysine) (PLL), palmitate (PAL), and deoxycholate (DOC): PEG-PEI (2P), PEG-PEI-PAL (3P), PEG-PLL (2P'), PEG-PLL-PAL (3P'), and PEG-PEI-DOC (2PD). In vitro transfection and western blot assays of luciferase using a colorectal cancer cell line expressing luciferase (HT29/LUC) concluded that 2P and 2P' caused no luciferase expression reduction while hydrophobically modified PNAs induced a 35-50% reduction (3P'<2PD<3P). Although cell viability remained stagnant, 3P triggered cellular stress responses including increased membrane porosity and decreased ATP and cellular protein concentrations. Raman spectroscopy suggested that hydrophobic groups influence PNA conformation changes, which may have caused over-ubiquitination and degradation of luciferase in the cells. These results indicate that hydrophobically modified PEG-PEI induces cellular distress causing over-ubiquitination of the luciferase protein, producing false positive siRNA transfection in the luciferase assay.
聚乙二醇共轭聚乙烯亚胺(PEG-PEI)是一种被广泛研究的阳离子聚合物,用于开发用于遗传疾病(包括癌症)的siRNA治疗的非病毒载体。稳定表达荧光素酶报告蛋白的细胞系通常用于评估siRNA/PEG-PEI复合物的转染效率,然而最近的研究发现PEG-PEI可以独立于siRNA降低荧光素酶的表达。本研究通过使用由PEG、PEI、聚-L-赖氨酸(PLL)、棕榈酸酯(PAL)和脱氧胆酸盐(DOC)制成的聚合物纳米组装体(PNA),即PEG-PEI(2P)、PEG-PEI-PAL(3P)、PEG-PLL(2P')、PEG-PLL-PAL(3P')和PEG-PEI-DOC(2PD),阐明了荧光素酶测定中假阳性效应的原因。使用表达荧光素酶的结肠癌细胞系(HT29/LUC)进行的荧光素酶体外转染和蛋白质印迹分析得出结论,2P和2P'不会导致荧光素酶表达降低,而疏水修饰的PNA会导致35-50%的降低(3P'<2PD<3P)。尽管细胞活力保持不变,但3P引发了细胞应激反应,包括膜孔隙率增加以及ATP和细胞蛋白浓度降低。拉曼光谱表明疏水基团影响PNA构象变化,这可能导致细胞内荧光素酶过度泛素化和降解。这些结果表明,疏水修饰的PEG-PEI会诱导细胞应激,导致荧光素酶蛋白过度泛素化,从而在荧光素酶测定中产生假阳性siRNA转染。