TY - JOUR
T1 - Efficient delivery of siRNA using dendritic poly(l-lysine) for loss-of-function analysis
AU - Inoue, Yusuke
AU - Kurihara, Ryosuke
AU - Tsuchida, Akiko
AU - Hasegawa, Mino
AU - Nagashima, Takeyuki
AU - Mori, Takeshi
AU - Niidome, Takuro
AU - Katayama, Yoshiki
AU - Okitsu, Osamu
N1 - Funding Information:
This work was financially supported by a grant-in-aid from the New Energy and Industrial Technology Development Organization (NEDO).
PY - 2008/2/18
Y1 - 2008/2/18
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=38549099191&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=38549099191&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2007.10.022
DO - 10.1016/j.jconrel.2007.10.022
M3 - Article
C2 - 18055057
AN - SCOPUS:38549099191
SN - 0168-3659
VL - 126
SP - 59
EP - 66
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 1
ER -