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首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >The Effect of IL-26 on TNF-?-Induced CXCL8 Responses by Colonic Epithelial Cell Lines
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The Effect of IL-26 on TNF-?-Induced CXCL8 Responses by Colonic Epithelial Cell Lines

机译:IL-26对TNF - α - 诱导的结肠上皮细胞系CXCL8响应的影响

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Th17 cells of the intestine and colon can produce several important cytokines during mucosal inflammation. However, few studies have focused on the role of IL-26 in intestinal inflammations. Colonic epithelial cells express receptors for IL-26, and this cytokine has been shown to induce the HT-29 colonic epithelial cell line to produce the chemokine CXCL8. However, epithelial cells would function in a cytokine network environment during mucosal inflammation and any effect of IL-26 on colonic epithelial cell chemokine responses could be affected by the presence of other potent pro-inflammatory cytokines like TNF-? and IL-1. Therefore, we investigated the effect of IL-26 with TNF-? or IL-1 on colonic epithelial cell line secretion of CXCL8. IL-26 alone had no effect on HT-29 or DLD1 cell line CXCL8 secretion. Yet, IL-26 was found to significantly enhance TNF-?-induced, but not IL-1-induced, CXCL8 secretion, but only at high levels of TNF-?. Similar results were seen with DLD1 cells. IL-26 did not enhance TNF-?-induced CXCL8 mRNA levels and did not affect TNF-?-induced I?B? phosphorylation or degradation. However, signaling through ERK and p38 MAPK were determined to be involved in the enhancing effect of IL-26 on the TNF-?-induced CXCL8 secretion, perhaps through known post-translational effects. These results suggest that the role of IL-26 in intestinal inflammation may be limited to enhancing CXCL8 secretion in the presence high levels of TNF-?, such as may occur in inflammatory bowel disease.
机译:肠和结肠的Th17细胞可以在粘膜炎症期间产生几个重要的细胞因子。然而,很少有研究专注于IL-26在肠道炎症中的作用。表达IL-26的结肠上皮细胞表达受体,并且已经显示该细胞因子诱导HT-29结肠上皮细胞系以产生趋化因子CXCL8。然而,上皮细胞在粘膜炎症期间在细胞因子网络环境中起作用,并且IL-26对结肠上皮细胞趋化因子的任何影响可能受到其他有效的促炎细胞因子(如TNF)的存在影响和IL-1。因此,我们调查了IL-26与TNF-的影响 - ?或IL-1关于结肠上皮细胞系CXCL8的分泌。单独对IL-26对HT-29或DLD1细胞系CXCL8分泌没有影响。然而,发现IL-26显着增强TNF - ? - 诱导的,但不是IL-1诱导的CXCL8分泌,但仅在高水平的TNF-?用DLD1细胞看到类似的结果。 IL-26没有增强TNF - ? - 诱导的CXCL8 mRNA水平,并没有影响TNF - ? - 诱导I?B?磷酸化或降解。然而,通过ERK和P38 MAPK的信号传导涉及IL-26对TNF - 诱导的CXCL8分泌的增强作用,或许通过已知的翻译后效应。这些结果表明IL-26在肠炎中的作用可能限于在存在高水平的TNF-β中增强CXCL8分泌,例如可能在炎性肠病中发生。

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