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作 者:赵砚丽[1] 郭娜[1] 岳立辉[1] 彭彦辉[2] 陈静[3] 卢大儒[3]
机构地区:[1]河北省人民医院麻醉科,石家庄市050051 [2]河北省人民医院普外科 [3]复旦大学遗传所
出 处:《中华麻醉学杂志》2008年第5期444-447,共4页Chinese Journal of Anesthesiology
基 金:国家自然科学基金资助项目(30672024)
摘 要:目的观察TAT-血红素氧合酶-1(HO-1)融合蛋白对L-02细胞的转导能力、细胞毒性和转导后细胞内HO-1活性,评价其转导效果。方法L-02细胞与FITC标记的TAT-HO-1融合蛋白孵育4h后,荧光显微镜下观察TAT-HO-1融合蛋白转导入L-02细胞的情况。L-02细胞与TAT-HO-1融合蛋白孵育4h后,采用CCK-8方法测定L-02细胞的活力,采用化学法测定HO-1活性。结果与FITC标记的TAT-HO-1融合蛋白孵育后,L-02细胞内均匀分布绿色荧光;与TAT-HO-1融合蛋白孵育后,L-02细胞活力无明显改变,HO-1活性明显升高。结论TAT-HO-1融合蛋白可有效地转导入L-02细胞,可明显提高细胞内HO-1活性,且无细胞毒性。Objective To investigate the transduction ability, cytotoxicity and intracellular heine oxygenase-1 (HO-1) activity of TAT-HO-1 fusion protein transduced into L-02 cells. Methods L-02 cells were incubated with FITC-labeled TAT-HO-1 fusion protein for 4 h and were then examined with fluorescence microscope for the transduction ability. After 4 h incubation with TAT-HO-1 fusion protein, viability of L-02 cells was detected by CCK-8 assay and HO-1 activity by chemical method. Results After incubation with FITC-labeled TAT:HO-1 fusion protein, green fluorescence could be observed in L-02 cells. The viability of L-02 cells did not change and HO-1 activity was significantly increased after incubation with TAT-HO-1 fusion protein. Conclusion TAT-HO-1 fusion protein can be effectively, transduced into L-02 ceils and HO-1 activity in L-02 cells is increased without cytotoxicity.
关 键 词:血红素氧化酶(脱环) 基因产物 tat 肝细胞
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