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热休克蛋白27(HSP27)增强成纤维细胞中超氧化物的产生并抵御热休克

Enhancement of superoxide production and protection against heat shock by HSP27 in fibroblasts.

作者信息

Souren J E, Van Aken H, Van Wijk R

机构信息

Department of Molecular Cell Biology, Utrecht University, The Netherlands.

出版信息

Biochem Biophys Res Commun. 1996 Oct 23;227(3):816-21. doi: 10.1006/bbrc.1996.1590.

Abstract

Extracellular superoxide production in the Chinese hamster CCL39 fibroblast cell line was detected by direct counting of luminol-enhanced chemiluminescence in the presence of horseradish peroxidase (HRP). This superoxide production, which is directly related to cell density, can be inhibited by diphenylene iodonium, a specific inhibitor of NADPH-oxidase. The O2- generation is transiently inhibited following exposure of the cells to elevated temperatures. To study the possible relationship between HSP27 and its modulation of NADPH-oxidase activity we measured the generation of O2- activity in CCL39 cells containing either the gene coding for human HSP27 or a mutant form of this gene leading to HSP27 unable to be phosphorylated. Cells with the enhanced expression of normal human HSP27 as well as the non-phosphorylatable protein exhibited a 20-fold higher superoxide production than control CCL39 cells. Furthermore, we demonstrate that accumulation of normal HSP27 appears to play a role in prevention of NADPH-oxidase inhibition by heat.

摘要

在中国仓鼠CCL39成纤维细胞系中,通过在辣根过氧化物酶(HRP)存在的情况下直接计数鲁米诺增强的化学发光来检测细胞外超氧化物的产生。这种与细胞密度直接相关的超氧化物产生可被二苯基碘鎓(一种NADPH氧化酶的特异性抑制剂)抑制。细胞暴露于高温后,O₂⁻的产生会被短暂抑制。为了研究热休克蛋白27(HSP27)与其对NADPH氧化酶活性的调节之间的可能关系,我们测量了含有编码人HSP27基因或该基因导致HSP27无法磷酸化的突变形式的CCL39细胞中O₂⁻活性的产生。正常人类HSP27以及不可磷酸化蛋白表达增强的细胞,其超氧化物产生量比对照CCL39细胞高20倍。此外,我们证明正常HSP27的积累似乎在预防热对NADPH氧化酶的抑制中起作用。

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