Efficient delivery of siRNA using dendritic poly(l-lysine) for loss-of-function analysis

• DOI: 10.1016/j.jconrel.2007.10.022
• Publication Date: 2007-12-01T05:14:59Z
• Authors: Yusuke Inoue; Ryosuke Kurihara; Akiko Tsuchida; Mino Hasegawa; Takeyuki Nagashima; Takeshi Mori; Takuro Niidome; Yoshiki Katayama; Osamu Okitsu
• Keywords: 0301 basic medicine; Dendrimers; Drug Carriers; Cell Survival; Gluconeogenesis; Protein Serine-Threonine Kinases; Transfection; Metformin; Rats; 03 medical and health sciences; Cell Line, Tumor; Animals; Polylysine; RNA Interference; Catecholamine Plasma Membrane Transport Proteins; RNA, Small Interfering; Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)

RNA interference (RNAi) is a valuable tool for the validation of gene identification and functional genomics. Previously, it was reported that 6th generation dendritic poly(L-lysine) (KG6) transfected DNA into several cultivated cell lines with high efficiency and without any cytotoxic effects. In this study, the potential of KG6 to be an efficient siRNA carrier is investigated. KG6 showed effective knockdown of GAPDH with low cytotoxicity in combination with the weak-base amphiphilic peptide, Endo-Porter. In addition, the knockdown of PEPCK, which is the rate-limiting enzyme for gluconeogenesis, led to a reduction in glucose production in rat hepatoma H4IIEC3 cells. Knockdown of organic cation transporter 1 (OCT1), which is thought to be the gene that influences metformin action, was shown to successfully diminish the ability of metformin to inhibit gluconeogenesis in H4IIEC3 cells. In conclusion, using a combination of KG6 and Endo-Porter, a model system in which genes that influence metformin action can be identified was successfully constructed.