Local delivery of siRNA using a biodegradable polymer application to enhance BMP-induced bone formation

被引:67
|
作者
Manaka, Tomoya [1 ]
Suzuki, Akinobu [1 ]
Takayama, Kazushi [1 ]
Imai, Yuuki [1 ]
Nakamura, Hiroaki [1 ]
Takaoka, Kunio [1 ]
机构
[1] Osaka City Univ, Grad Sch Med, Dept Orthopaed Surg, Osaka 5458585, Japan
关键词
siRNA; Polymer; BMP; Noggin; Bone regeneration; MORPHOGENETIC PROTEIN-2; PHOSPHODIESTERASE INHIBITOR; ADENOSINE-MONOPHOSPHATE; PARATHYROID-HORMONE; RNA INTERFERENCE; NOGGIN; NANOPARTICLES; EXPRESSION; OSTEOBLAST; SYSTEM;
D O I
10.1016/j.biomaterials.2011.08.026
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Small interfering RNA (siRNA) is useful tool for specific and efficient knockdown of disease-related genes. However, in vivo applications of siRNA are limited due to difficulty in its efficient delivery to target cells. In this study, we investigated the efficacy of a biodegradable hydrogel, poly-D,L-lactic acid-p-dioxanone-polyethylene glycol block co-polymer (PLA-DX-PEG), as a siRNA carrier. PLA-DX-PEG pellets with or without fluorescein-labeled dsRNA were implanted into mouse dosal muscle pouches. The cellular uptake of dsRNA surround the polymer was confirmed by fluorescent microscopy. The fluorescence intensity was dose-dependent of the dsRNA, and exhibited a time-dependent decrease. To investigate its biological efficiency, noggin (antagonoist to BMPs) gene-silencing with siRNA (siRNA/Noggin) was examined by the amount of suppression of BMP-2-induced noggin expression and the level of performance of BMP, indicated by ectopic bone formation. Noggin gene expression induced by BMP-2 was suppressed by addition of siRNA/Noggin to the implant, and the ectopic bone formation induced by implants with both BMP-2 and siRNA/Noggin was significantly greater than those induced by implants with BMP-2 alone. These results indicate the efficacy of local delivery of siRNAs by PLA-DX-PEG polymer, which intensified bone-inducing effects of BMP and promoted new bone formation by suppressing gene expression of Noggin. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9642 / 9648
页数:7
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