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首页> 外文期刊>Pharmacological research: The official journal of The Italian Pharmacological Society >Bacterial redox protein azurin induce apoptosis in human osteosarcoma U2OS cells.
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Bacterial redox protein azurin induce apoptosis in human osteosarcoma U2OS cells.

机译:细菌氧化还原蛋白天青蛋白诱导人骨肉瘤U2OS细胞凋亡。

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摘要

As a low molecular weight redox protein elaborated from the pathogenic bacteria Pseudomonas aeruginosa, azurin is one of representative bacterial products applied in the treatment of tumour. We found that the growth of U2OS cells was significantly inhibited by azurin in a dose-dependent manner with the IC(50) value of 114.54+/-7.65 mgl(-1). But the growth of MG63 cells or L02 cells was almost not inhibited by azurin (P<0.05). Moreover, when treated with azurin, U2OS cells showed typical apoptotic morphological features observed by fluorescent microscopy (AO and Hoechst 33258) and transmission electron microscopy. Typical DNA "ladder" bands were also observed. The apoptosis rate was 35.8% tested by fluorescence-activated cell sorter (Annexin-V-FITC(+)/PI(-)) and the cell-cycle arrested in G(1) phase. But no apoptotic features were observed in control cells. The down-regulation of Bcl-2 (an inhibitor of apoptosis) were detected in U2OS cells when azurin was added for 24h. In contrast, the level of Bax and caspase-3 were significantly up-regulated. So we concluded that azurin could selectively induce apoptosis of human osteosarcoma U2OS cells and the induction of apoptosis by azurin was closely associated with down-regulation of Bcl-2, up-regulation of Bax and activation of caspase-3.
机译:作为从致病性细菌铜绿假单胞菌(Pseudomonas aeruginosa)精制的低分子量氧化还原蛋白,天青素是用于治疗肿瘤的代表性细菌产品之一。我们发现Azurin以剂量依赖性方式显着抑制U2OS细胞的生长,其IC(50)值为114.54 +/- 7.65 mgl(-1)。但是,天青蛋白几乎没有抑制MG63细胞或L02细胞的生长(P <0.05)。此外,用天青蛋白处理后,U2OS细胞表现出典型的凋亡形态特征,这是通过荧光显微镜(AO和Hoechst 33258)和透射电子显微镜观察到的。还观察到典型的DNA“阶梯”带。通过荧光激活细胞分选仪(Annexin-V-FITC(+)/ PI(-))测试的细胞凋亡率为35.8%,细胞周期停滞在G(1)期。但在对照细胞中未观察到凋亡特征。加入天青素24h后,在U2OS细胞中检测到Bcl-2(凋亡抑制剂)的下调。相反,Bax和caspase-3的水平显着上调。因此我们得出结论,天青蛋白可以选择性诱导人骨肉瘤U2OS细胞凋亡,天青蛋白诱导的凋亡与Bcl-2的下调,Bax的上调和caspase-3的激活密切相关。

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