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Regulation of interleukin 6 production in a human gastric epithelial cell line MKN-28.

机译:人胃上皮细胞系MKN-28中白介素6产生的调节。

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Interleukin (IL-) 6 is closely related to gastrointestinal diseases. The question of whether gastric epithelial cell contributes to IL-6 production remains undefined. We aim to evaluate the regulatory pathway of IL-6 expression in gastric epithelial cells, by using different inflammatory cytokines, endotoxin, or protein kinase modulators. IL-6 was measured by ELISA. Phorbol-12-myristate-13-acetate (PMA), calcium ionophore A23187, TNF-alpha, IL-1beta, oncostatin M (OSM) but not lipopolysaccharide stimulated IL-6 production from gastric epithelial cell line MKN-28. Blocking protein tyrosine kinase (PTK) activation by herbimycin A or genistein, or blocking NF-kappaB activation by pyrrolidinedithiocarbamate, reduced the IL-6 expression induced by TNF-alpha, IL-1beta and OSM. Dexamethasone mimicked this effect. Protein kinase (PK) C inhibitor only reduced the PMA and OSM induced IL-6 production. Both inhibitors and activators for PKA and G-protein as well as IL-10 had no effects on IL-6 expression. These results indicate that inflammatory cytokines are crucial for IL-6 regulation in gastric epithelial cells. The IL-6 signal pathway is mediated through PTK, NF-kappaB, and also involve PKC, intracellular calcium and sensitive to dexamethasone, but is not related to PKA, G-protein and IL-10. Copyright 2000 Academic Press.
机译:白介素(IL-)6与胃肠道疾病密切相关。胃上皮细胞是否有助于IL-6产生的问题仍然不确定。我们旨在通过使用不同的炎症细胞因子,内毒素或蛋白激酶调节剂来评估胃上皮细胞中IL-6表达的调控途径。通过ELISA测量IL-6。 Phorbol-12-肉豆蔻酸酯-13-乙酸酯(PMA),钙离子载体A23187,TNF-α,IL-1beta,抑瘤素M(OSM)而非脂多糖刺激胃上皮细胞系MKN-28分泌IL-6。通过除草霉素A或染料木黄酮阻止蛋白酪氨酸激酶(PTK)激活,或通过吡咯烷二硫代氨基甲酸酯阻止NF-κB激活,降低了TNF-α,IL-1beta和OSM诱导的IL-6表达。地塞米松模仿了这种作用。蛋白激酶(PK)C抑制剂只能减少PMA和OSM诱导的IL-6产生。 PKA和G蛋白以及IL-10的抑制剂和激活剂对IL-6的表达均无影响。这些结果表明,炎性细胞因子对于胃上皮细胞中IL-6的调节至关重要。 IL-6信号途径是通过PTK,NF-κB介导的,并且还涉及PKC,细胞内钙和对地塞米松敏感,但与PKA,G蛋白和IL-10不相关。版权所有2000学术出版社。

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