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Viral Induction of Inflammatory Cytokines in Human Epithelial Cells Follows a p38 Mitogen-Activated Protein Kinase-Dependent but NF-κB-Independent Pathway

机译:人体上皮细胞中炎性细胞因子的病毒诱导遵循p38丝裂原活化的蛋白激酶依赖性,但不依赖NF-κB的途径。

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The initial step in an immune response toward a viral infection is the induction of inflammatory cytokines. This innate immune response is mediated by expression of a variety of cytokines exemplified by TNF-α and IL-1β. A key signal for the recognition of intracellular viral infections is the presence of dsRNA. Viral infections and dsRNA treatment can activate several signaling pathways including the protein kinase R pathway, mitogen-activated protein kinase (MAPK) pathways, and NF-κB, which are important in the expression of inflammatory cytokines. We previously reported that activation of protein kinase R was required for dsRNA induction of TNF-α, but not for IL-1β. In this study, we report that activation of the p38 MAPK pathway by respiratory viral infections is necessary for induction of inflammatory cytokines in human bronchial epithelial cells. Inhibition of p38 MAPK by two different pharmacological inhibitors showed that expression of both TNF-α and IL-1β required activation of this signaling pathway. Interestingly, inhibition of NF-κB did not significantly reduce viral induction of either cytokine. Our data show that, during the initial infections of epithelial cells with respiratory viruses, activation of the p38 MAPK pathway is associated with induction of inflammation, and NF-κB activation may be less important than previously suggested.
机译:对病毒感染的免疫反应的第一步是诱导炎性细胞因子。这种先天的免疫应答是由多种细胞因子的表达介导的,例如TNF-α和IL-1β。识别细胞内病毒感染的关键信号是dsRNA的存在。病毒感染和dsRNA处理可以激活几种信号传导途径,包括蛋白激酶R途径,促分裂原活化蛋白激酶(MAPK)途径和NF-κB,这在炎症性细胞因子的表达中很重要。我们先前曾报道过,dsRNA诱导TNF-α需要激活蛋白激酶R,而IL-1β则不需要。在这项研究中,我们报道呼吸道病毒感染激活p38 MAPK通路对于诱导人支气管上皮细胞中的炎性细胞因子是必要的。两种不同的药理抑制剂对p38 MAPK的抑制作用表明,TNF-α和IL-1β的表达都需要激活该信号通路。有趣的是,对NF-κB的抑制并没有显着降低任一细胞因子的病毒诱导。我们的数据表明,在呼吸道病毒感染上皮细胞的初始过程中,p38 MAPK途径的激活与炎症的诱导有关,而NF-κB的激活可能不如先前所建议的重要。

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