Murata R, Nakagawa K, Ohtori S, Ochiai N, Arai M, Saisu T, Sasho T, Takahashi K, Moriya H
Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Osteoarthritis Cartilage. 2007 Nov;15(11):1275-82. doi: 10.1016/j.joca.2007.04.001. Epub 2007 May 29.
The purpose of this study was to develop a new technique of gene transfer utilizing radial shock waves. The effects of radial shock waves on gene transfer in rabbit chondrocytes were examined by varying the parameters of exposure conditions in vitro.
Chondrocytes were obtained from New Zealand white rabbits and cultured in a monolayer. A luciferase-encoding gene expression vector, or vector alone, was added to chondrocyte cell suspensions, and the cells were then exposed to radial shock waves. Parameters such as pressure amplitude, number of pulses, frequency, and DNA concentration were varied, and luciferase activity was measured 48h after transfection. Transfection efficiency of radial shock waves was compared with the FuGENE6 transfection method using a green fluorescence protein (GFP)-encoding gene vector by fluorescent-activated cell sorter (FACS) analysis.
Radial shock wave exposure significantly increased luciferase activity over 140-fold as compared to the control under the optimal exposure conditions. Both pressure amplitude and number of pulses were relevant to transfection efficiency and cell viability, but frequency was not. Transfection efficiency increased in a dose-dependent manner with DNA concentration. FACS analysis showed 4.74% of GFP-encoding gene using radial shock waves. FuGENE6 transfection was almost similar in transfection efficiency to radial shock wave.
In spite of certain degree of cell disruption, radial shock waves significantly augmented reporter gene transfection in rabbit chondrocytes in vitro. Radial shock waves may potentially contribute to the treatment of the cartilage morbidities by enhancing the potency of tissue healing and gene transfection of growth factors.
本研究旨在开发一种利用径向冲击波的基因转移新技术。通过在体外改变暴露条件参数,研究径向冲击波对兔软骨细胞基因转移的影响。
从新西兰白兔获取软骨细胞并进行单层培养。将编码荧光素酶的基因表达载体或单独的载体添加到软骨细胞悬液中,然后使细胞暴露于径向冲击波。改变诸如压力幅值、脉冲数、频率和DNA浓度等参数,并在转染后48小时测量荧光素酶活性。使用荧光激活细胞分选仪(FACS)分析,将径向冲击波的转染效率与使用绿色荧光蛋白(GFP)编码基因载体的FuGENE6转染方法进行比较。
在最佳暴露条件下,与对照组相比,径向冲击波暴露使荧光素酶活性显著增加超过140倍。压力幅值和脉冲数均与转染效率和细胞活力相关,但频率无关。转染效率随DNA浓度呈剂量依赖性增加。FACS分析显示,使用径向冲击波时,4.74%的细胞转染了GFP编码基因。FuGENE6转染的转染效率与径向冲击波几乎相似。
尽管存在一定程度的细胞破坏,但径向冲击波在体外显著增强了兔软骨细胞中报告基因的转染。径向冲击波可能通过增强组织愈合能力和生长因子的基因转染,对软骨疾病的治疗有潜在贡献。