Cho S, Urata Y, Iida T, Goto S, Yamaguchi M, Sumikawa K, Kondo T
Department of Biochemistry and Molecular Biology in Disease, Nagasaki University School of Medicine, Japan.
Biochem Biophys Res Commun. 1998 Dec 9;253(1):104-8. doi: 10.1006/bbrc.1998.9697.
Nuclear factor-kappa B (NF-kappa B) regulates gene expression upon immune and inflammatory responses. It has been demonstrated that redox regulation by thiols is involved in the signal-transduction cascade. In this study, we examined the effect of glutathione (GSH) on the NF-kappa B activity and the expression of NF-kappa B subunits induced by tumor necrosis factor-alpha (TNF-alpha) using mouse vascular endothelial cells. GSH inhibited the serine phosphorylation of I kappa B-alpha by TNF-alpha, leading to the downregulation of NF-kappa B-DNA binding activity followed by decreased expression of p65/p50 and I kappa B mRNAs. The regulation of the autoregulatory loop for the NF-kappa B activation and the expression of NF-kappa B subunits may be important in endothelial cells in response to cytokines.
核因子-κB(NF-κB)在免疫和炎症反应中调节基因表达。已有研究表明,硫醇的氧化还原调节参与信号转导级联反应。在本研究中,我们使用小鼠血管内皮细胞研究了谷胱甘肽(GSH)对肿瘤坏死因子-α(TNF-α)诱导的NF-κB活性及NF-κB亚基表达的影响。GSH抑制TNF-α诱导的IκB-α丝氨酸磷酸化,导致NF-κB-DNA结合活性下调,随后p65/p50和IκB mRNA表达降低。NF-κB激活的自动调节环及NF-κB亚基的表达调控在内皮细胞对细胞因子的反应中可能很重要。