首页> 外文期刊>Photochemistry and Photobiology: An International Journal >ELEVATION OF GRP-78 AND LOSS OF HSP-70 FOLLOWING PHOTODYNAMIC TREATMENT OF V79 CELLS - SENSITIZATION BY NIGERICIN
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ELEVATION OF GRP-78 AND LOSS OF HSP-70 FOLLOWING PHOTODYNAMIC TREATMENT OF V79 CELLS - SENSITIZATION BY NIGERICIN

机译:光敏处理V79细胞后GRP-78升高和HSP-70缺失-尼日利亚霉素致敏

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摘要

Chinese hamster V79 cells were treated with photodynamic therapy (PDT) sensitized by aluminum phthalocyanine (AlPc) or with the ionophore nigericin or with combinations of PDT and nigericin. We previously showed that PDT and nigericin interact synergistically in the killing of these cells; i.e. doses of PDT that kill no more than 10% of the cells in combination with nontoxic exposures to nigericin lead to a loss of clonogenicity of three to five orders of magnitude. Photodynamic therapy induces an enhanced rate of expression of the stress gene grp-78 both at the transcriptional and translational levels and causes a decrease in the synthesis of the constitutive heat shock protein HSP-70 as well as in expression of HSP-70 mRNA. When the cells are exposed to PDT in the presence of nigericin, these effects are elicited at three- to four-fold lower PDT doses. Thus, PDT in the presence of nigericin is much more effective in inducing the changes in gene expression than is PDT alone. In the absence of nigericin the PDT dose inducing a two-fold increase in GRP-78 accumulation causes little or no loss of clonogenicity. In the presence of nigericin, however, the PDT dose leading to a similar change in GRP-78 level produces up to a 50% loss of clonogenicity. The fact that nigericin is dose-modifying for both cell killing and stress responses suggests that nigericin either increases the yield of oxidative damage from a given dose of PDT or magnifies the cellular response to a constant level of oxidative stress. [References: 45]
机译:对中国仓鼠V79细胞进行光动力学疗法(PDT),以铝酞菁(AlPc)敏化,或以离子载体尼日利亚菌素或PDT和尼日利亚菌素组合治疗。先前我们显示,PDT和尼日利亚霉素在杀死这些细胞中具有协同作用。即,杀死不超过10%的细胞的PDT剂量与无毒暴露于黑霉素的组合会导致三到五个数量级的克隆形成性丧失。光动力疗法在转录和翻译水平上均诱导了应激基因grp-78的表达率提高,并导致组成型热休克蛋白HSP-70的合成以及HSP-70 mRNA的表达下降。当细胞在尼日利亚菌素存在下暴露于PDT时,这些作用是在较低PDT剂量的三至四倍时引起的。因此,在存在尼日利亚霉素的情况下,PDT比单独的PDT更有效地诱导基因表达的变化。在缺乏尼日利亚霉素的情况下,PDT剂量诱导GRP-78积累增加两倍,导致克隆形成性的降低很小或没有。但是,在存在尼日利亚霉素的情况下,导致类似的GRP-78水平变化的PDT剂量会导致克隆形成性损失高达50%。黑霉菌素对细胞杀伤和应激反应均具有剂量调节性的事实表明,黑霉菌素可增加给定剂量的PDT产生的氧化损伤的产生,或将细胞应答放大至恒定水平的氧化应激。 [参考:45]

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