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首页> 外文期刊>Comparative biochemistry and physiology, Part A. Molecular and integrative physiology >Comparison of the effect of heat shock factor inhibitor, KNK437, on heat shock- and chemical stress-induced hsp30 gene expression in Xenopus laevis A6 cells
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Comparison of the effect of heat shock factor inhibitor, KNK437, on heat shock- and chemical stress-induced hsp30 gene expression in Xenopus laevis A6 cells

机译:热休克因子抑制剂KNK437对热休克和化学应激诱导的非洲爪蟾A6细胞中hsp30基因表达影响的比较

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In this study, we compared the effect of KNK437 (N-formyl-3, 4-methylenedioxy-benzylidene-γ-butyrolactam), a benzylidene lactam compound, on heat shock and chemical stressor-induced hsp30 gene expression in Xenopus laevis A6 kidney epithelial cells. Previously, KNK437 was shown to inhibit HSE-HSF1 binding activity and heat-induced hsp gene expression. In the present study, Northern and Western blot analysis revealed that pretreatment of A6 cells with KNK437 inhibited hsp30 mRNA and HSP30 and HSP70 protein accumulation induced by chemical stressors including sodium arsenite, cadmium chloride and herbimycin A. In A6 cells subjected to sodium arsenite, cadmium chloride, herbimycin A or a 33 °C heat shock treatment, immunocytochemistry and confocal microscopy revealed that HSP30 accumulated primarily in the cytoplasm. However, incubation of A6 cells at 35 °C resulted in enhanced HSP30 accumulation in the nucleus. Pre-treatment with 100 μM KNK437 completely inhibited HSP30 accumulation in A6 cells heat shocked at 33 or 35 °C as well as cells treated with 10 μM sodium arsenite, 100 μM cadmium chloride or 1 μg/mL herbimycin A. These results show that KNK437 is effective at inhibiting both heat shock- and chemical stress-induced hsp gene expression in amphibian cells.
机译:在这项研究中,我们比较了亚苄基内酰胺化合物KNK437(N-甲酰基-3,4-亚甲二氧基-亚苄基-γ-丁内酰胺)对非洲爪蟾A6肾上皮热休克和化学应激诱导的hsp30基因表达的影响。细胞。以前,已显示KNK437抑制HSE-HSF1结合活性和热诱导的hsp基因表达。在本研究中,Northern和Western印迹分析显示,用KNK437预处理A6细胞可抑制由化学应激物(包括亚砷酸钠,氯化镉和除草霉素A)诱导的hsp30 mRNA和HSP30和HSP70蛋白积累。在受亚砷酸钠,镉污染的A6细胞中氯化物,除草素A或33°C的热休克处理,免疫细胞化学和共聚焦显微镜检查表明,HSP30主要在细胞质中积累。但是,在35°C下孵育A6细胞会导致HSP30在细胞核中的积累增强。用100μMKNK437预处理可以完全抑制HSP30在33或35°C热激的A6细胞以及用10μM亚砷酸钠,100μM氯化镉或1μg/ mL除草霉素A处理的细胞中的HSP30积累。这些结果表明,KNK437在抑制热休克和化学应激诱导的两栖动物热休克蛋白基因表达方面有效。

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