首页> 外文期刊>International journal of medical microbiology: IJMM >Enterohemorrhagic Escherichia coli O157 outer membrane vesicles induce interleukin 8 production in human intestinal epithelial cells by signaling via Toll-like receptors TLR4 and TLR5 and activation of the nuclear factor NF-kappa B
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Enterohemorrhagic Escherichia coli O157 outer membrane vesicles induce interleukin 8 production in human intestinal epithelial cells by signaling via Toll-like receptors TLR4 and TLR5 and activation of the nuclear factor NF-kappa B

机译:Enterohemorlagic大肠杆菌O157外膜囊泡通过通过Toll样受体TLR4和TLR5发信号传导和核因子NF-Kappa B的激活来诱导人肠道上皮细胞中的白细胞介素8产生。NF-Kappa B的激活

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摘要

Proinflammatory cytokines play important roles in the pathogenesis of diseases caused by enterohemorrhagic Escherichia calf (EHEC) O157, but the spectrum of bacterial components involved in the proinflammatory responses is not fully understood. Here, we investigated the abilities of outer membrane vesicles (OMVs), nanoparticles released by EHEC O157 during growth, to induce production of proinflammatory cytokines in human intestinal epithelial cells. OMVs from both EHEC O157:H7 and sorbitol-fermenting (SF) EHEC O157:H- induced production of interleukin-8 (IL-8) in Caco-2, HCT-8, and HT-29 intestinal epithelial cell lines. H7 flagellin was the key IL-8-inducing component of EHEC O157:H7 OMVs, whereas cytolethal distending toxin V and O157 lipopolysaccharide (LPS) largely contributed to IL-8 production elicited by flagellin-lacking OMVs from SF EHEC O157:H-. The H7 flagellin-mediated signaling via Toll-like receptor (TLR) 5, and O157 LPS-mediated signaling via TLR4/MD-2 complex, which were followed by activation of the nuclear factor NE-kappa B were major pathways underlying IL-8 production induced by EHEC O157 OMVs. The proinflammatory and immunomodulatory capacities of EHEC O157 OMVs have pathogenetic implications and support the OMVs as suitable vaccine candidates.
机译:促炎细胞因子在肠溶性大肠杆菌(EHEC)O157引起的疾病发病机制中起重要作用,但临床反应中涉及的细菌组分的光谱尚未完全理解。在这里,我们研究了在生长期间通过EHEC O157释放的外膜囊泡(OMV),纳米颗粒的能力,诱导人肠上皮细胞中促炎细胞因子的产生。来自EHEC O157:H7和山梨糖醇发酵(SF)EHEC O157:H-诱导在Caco-2,HCT-8和HT-29肠上皮细胞系中产生白细胞介素-8(IL-8)的产生。 H7鞭毛蛋白是EHEC O157:H7 OMV的关键IL-8诱导组分,而细胞素伸长的毒素V和O157脂多糖(LPS)主要导致由SF EHEC O157的鞭毛蛋白缺失的OMV引发的IL-8产生:H-。通过TLR4 / MD-2复合物通过Toll样受体(TLR)5和O157 LPS介导的信号传导H7鞭毛蛋白介导的信号传导,然后通过TLR4 / MD-2复合物进行核因子Ne-Kappa B的激活是IL-8的主要途径EHEC O157 OMV引起的生产。 EHEC O157 OMV的促炎和免疫调节能力具有致病性意义并支持OMV作为合适的疫苗候选者。

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