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肠出血性大肠杆菌 O157 外膜囊泡通过 Toll 样受体 TLR4 和 TLR5 信号转导和核因子 NF-κB 的激活诱导人肠道上皮细胞产生白细胞介素 8。

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-κB.

机构信息

Institute for Hygiene and the National Consulting Laboratory for Hemolytic Uremic Syndrome, University of Münster, Münster, 48149, Germany; National Institute of Public Health, National Reference Laboratory for E. coli and Shigella, Prague, 100 42, Czech Republic.

National Institute of Public Health, National Reference Laboratory for E. coli and Shigella, Prague, 100 42, Czech Republic.

出版信息

Int J Med Microbiol. 2018 Oct;308(7):882-889. doi: 10.1016/j.ijmm.2018.06.004. Epub 2018 Jun 19.

Abstract

Proinflammatory cytokines play important roles in the pathogenesis of diseases caused by enterohemorrhagic Escherichia coli (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 NF-κB 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.

摘要

促炎细胞因子在肠出血性大肠杆菌 (EHEC) O157 引起的疾病发病机制中发挥重要作用,但涉及促炎反应的细菌成分谱尚不完全清楚。在这里,我们研究了在生长过程中由 EHEC O157 释放的外膜囊泡 (OMV),即纳米颗粒,在诱导人肠上皮细胞产生促炎细胞因子方面的能力。EHEC O157:H7 和山梨醇发酵 (SF) EHEC O157:H 的 OMV 均可诱导 Caco-2、HCT-8 和 HT-29 肠上皮细胞系产生白细胞介素-8 (IL-8)。H7 鞭毛蛋白是 EHEC O157:H7 OMV 诱导 IL-8 的关键成分,而细胞毒性扩张毒素 V 和 O157 脂多糖 (LPS) 则主要导致 SF EHEC O157:H 的鞭毛蛋白缺失 OMV 诱导的 IL-8 产生。H7 鞭毛蛋白通过 Toll 样受体 (TLR) 5 介导的信号转导,以及 O157 LPS 通过 TLR4/MD-2 复合物介导的信号转导,随后 NF-κB 核因子被激活,这是 EHEC O157 OMV 诱导 IL-8 产生的主要途径。EHEC O157 OMV 的促炎和免疫调节能力具有发病意义,并支持 OMV 作为合适的疫苗候选物。

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