首页> 外文期刊>Free radical research >Monochloramine inhibits the expression of E-selectin and intercellular adhesion molecule-1 induced by TNF-alpha through the suppression of NF-kappaB activation in human endothelial cells.
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Monochloramine inhibits the expression of E-selectin and intercellular adhesion molecule-1 induced by TNF-alpha through the suppression of NF-kappaB activation in human endothelial cells.

机译:一氯胺通过抑制人内皮细胞中NF-κB的活化来抑制TNF-α诱导的E-选择蛋白和细胞间粘附分子1的表达。

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Reactive oxygen species have various effects on the expression of cell adhesion molecules induced by proinflammatory cytokines, such as tumor necrosis factor a (T-NF-alpha). We studied the effects of monochloramine (NH2Cl), a physiological oxidant derived from activated neutrophils, on the TNF-alpha-induced expression of e-selectin and intercellular adhesion molecule-1 (ICAM-1) in human umbilical vein endothelial cells (HUVEC). HUVEC were pretreated with or without NH2Cl (20-90 microM for 20 min), then stimulated with TNF-alpha (10 ng/ml), and the expression of e-selectin and ICAM-1 was measured. Without NH2Cl, TNF-alpha induced marked expression of e-selectin and ICAM-1. Pretreatment with NH2Cl resulted in a significant, but transient inhibition of the expression of adhesion molecules. Higher dose of NH2Cl showed more pronounced inhibition, and the inhibitory effect lasted for 8h when 70 microM of NH2Cl was added. TNF-alpha stimulation also induced marked activation of nuclear factor KB (NF-kappaB). Notably, NH2Cl also inhibited this NF-kappaB activation in a dose- and time-dependent manner, which was similar to the inhibition of e-selectin and ICAM-1 expression. In addition, IkappaB-alpha phosphorylation and degradation were also inhibited by NH2Cl pretreatment. These observations indicated that NH2Cl inhibited TNF-alpha-induced expression of e-selectin and ICAM-1 through the inhibition of NF-kappaB activation. We speculate that neutrophil-derived chloramines may have a regulatory role in the recruitment of leukocytes.
机译:活性氧对促炎细胞因子(例如肿瘤坏死因子a(T-NF-alpha))诱导的细胞粘附分子的表达具有多种影响。我们研究了一氯胺(NH2Cl),一种由活化的中性粒细胞衍生的生理氧化剂,对人脐静脉内皮细胞(HUVEC)TNF-α诱导的e-选择素和细胞间粘附分子1(ICAM-1)表达的影响。 。在有或没有NH2Cl(20-90 microM持续20分钟)的情况下对HUVEC进行预处理,然后用TNF-α(10 ng / ml)刺激,并测量e-选择素和ICAM-1的表达。没有NH2Cl,TNF-α诱导e-选择素和ICAM-1的明显表达。用NH2Cl预处理可显着但短暂地抑制粘附分子的表达。较高剂量的NH2Cl表现出更明显的抑制作用,当添加70 microM NH2Cl时抑制作用持续8h。 TNF-α刺激还诱导了核因子KB(NF-κB)的明显活化。值得注意的是,NH2Cl还以剂量和时间依赖性的方式抑制了NF-κB的活化,这与抑制e-选择素和ICAM-1的表达相似。此外,NH2Cl预处理还抑制了IkappaB-α的磷酸化和降解。这些观察结果表明,NH 2 Cl通过抑制NF-κB活化而抑制了TNF-α诱导的e-选择素和ICAM-1的表达。我们推测中性粒细胞来源的氯胺可能在白细胞募集中具有调节作用。

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