Peng H B, Libby P, Liao J K
Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.
J Biol Chem. 1995 Jun 9;270(23):14214-9. doi: 10.1074/jbc.270.23.14214.
To determine the mechanism(s) by which the endogenous mediator nitric oxide (NO) inhibits the activation of transcription factor NF-kappa B, we stimulated human vascular endothelial cells with tumor necrosis factor-alpha in the presence of two NO donors, sodium nitroprusside and S-nitrosoglutathione. Electrophoretic mobility shift assays demonstrated that both NO donors inhibited NF-kappa B activation by tumor necrosis factor-alpha. This effect was not mediated by guanylyl cyclase activation since the cGMP analogue 8-bromo-cGMP had no similar effect. Inhibition of endogenous constitutive NO production by L-N-monomethylarginine, however, activated NF-kappa B, suggesting tonic inhibition of NF-kappa B under basal conditions. NO had little or no effects on other nuclear binding proteins such as AP-1 and GATA. Immunoprecipitation studies showed that NO stabilized the NF-kappa B inhibitor, I kappa B alpha, by preventing its degradation from NF-kappa B. NO also increased the mRNA expression of I kappa B alpha, but not NF-kappa B subunits, p65 or p50, and transfection experiments with a chloramphenicol acetyltransferase reporter gene linked to the I kappa B alpha promoter suggested transcriptional induction of I kappa B alpha by NO. We propose that the induction and stabilization of I kappa B alpha by NO are important mechanisms by which NO inhibits NF-kappa B and attenuate atherogenesis.
为了确定内源性介质一氧化氮(NO)抑制转录因子NF-κB激活的机制,我们在两种NO供体硝普钠和S-亚硝基谷胱甘肽存在的情况下,用肿瘤坏死因子-α刺激人血管内皮细胞。电泳迁移率变动分析表明,两种NO供体均抑制肿瘤坏死因子-α诱导的NF-κB激活。由于环磷酸鸟苷(cGMP)类似物8-溴-cGMP没有类似作用,因此这种效应不是由鸟苷酸环化酶激活介导的。然而,L-N-单甲基精氨酸抑制内源性组成型NO生成可激活NF-κB,这表明在基础条件下NF-κB受到张力抑制。NO对其他核结合蛋白如活化蛋白-1(AP-1)和GATA几乎没有影响。免疫沉淀研究表明,NO通过防止NF-κB抑制因子IκBα降解来使其稳定。NO还增加了IκBα的mRNA表达,但不影响NF-κB亚基p65或p50的表达,并且用与IκBα启动子相连的氯霉素乙酰转移酶报告基因进行的转染实验表明NO可转录诱导IκBα。我们提出,NO诱导和稳定IκBα是NO抑制NF-κB并减轻动脉粥样硬化形成的重要机制。