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鼠伤寒沙门氏菌孔蛋白诱导U937细胞中细胞因子mRNA表达受不同磷酸化途径调控。

Induction of cytokine mRNA expression in U937 cells by Salmonella typhimurium porins is regulated by different phosphorylation pathways.

作者信息

Galdiero Marilena, Tortora Annalisa, Damiano Nicola, Vitiello Mariateresa, Longanella Anna, Galdiero Emilia

机构信息

Dipartimento di Medicina Sperimentale, Facoltà di Medicina e Chirurgia, Seconda Università degli Studi di Napoli, via De Crecchio, Napoli, Italy.

出版信息

Med Microbiol Immunol. 2005 Jan;194(1-2):13-23. doi: 10.1007/s00430-003-0209-7.

Abstract

Lipopolysaccharide (LPS) and porins of Gram-negative outer membranes are the main pathogenic factors implicated in the clinical syndrome of septic shock. The biological activity of porins and LPS are similar, but they occur by different mechanisms. It seems that porins act through different intracellular pathways with respect to LPS. In this study we analyzed the role of several inhibitors of the MEK/ERK signal pathway on the induction of proinflammatory and immunological cytokines in U937 cell line stimulated by Salmonella typhimurium porins and compared it to the cytokine induction after LPS stimulation. We investigated the effects of p38 MAP kinase inhibitor SB-203580, MEK/ERK kinase inhibitor PD-098059 and Raf-1 inhibitor forskolin, and demonstrated that they modulate cytokine mRNA expression in a different manner as a consequence of the use of porins or LPS as stimuli. TNF-alpha and IL-1beta mRNA expression is decreased by PD-098059 after stimulation with LPS but not with porins in differentiated U937 cells. IL-10 mRNA expression is inhibited by SB-203580 and PD-098059 after stimulation with porins in U937 cells. IL-6 and IL-8 mRNA expression is not changed by PD-098059 or SB-203580, after stimulation either with porins or LPS. Furthermore, mRNA expression of the studied cytokines, except for GM-CSF, is not changed using forskolin.

摘要

革兰氏阴性菌外膜的脂多糖(LPS)和孔蛋白是脓毒症休克临床综合征的主要致病因素。孔蛋白和LPS的生物活性相似,但作用机制不同。与LPS相比,孔蛋白似乎通过不同的细胞内途径发挥作用。在本研究中,我们分析了几种MEK/ERK信号通路抑制剂对鼠伤寒沙门氏菌孔蛋白刺激的U937细胞系中促炎和免疫细胞因子诱导的作用,并将其与LPS刺激后的细胞因子诱导作用进行比较。我们研究了p38丝裂原活化蛋白激酶抑制剂SB - 203580、MEK/ERK激酶抑制剂PD - 098059和Raf - 1抑制剂福斯可林的作用,结果表明,由于使用孔蛋白或LPS作为刺激物,它们以不同方式调节细胞因子mRNA表达。在分化的U937细胞中,用LPS刺激后,PD - 098059可降低TNF-α和IL - 1β mRNA表达,但用孔蛋白刺激则无此效果。在U937细胞中,用孔蛋白刺激后,SB - 203580和PD - 098059可抑制IL - 10 mRNA表达。用孔蛋白或LPS刺激后,PD - 098059或SB - 203580对IL - 6和IL - 8 mRNA表达无影响。此外,除GM - CSF外,使用福斯可林对所研究细胞因子的mRNA表达无影响。

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