• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

霍乱弧菌外膜蛋白U诱导人肠上皮细胞中白细胞介素-8的表达。

Vibrio cholerae OmpU induces IL-8 expression in human intestinal epithelial cells.

作者信息

Yang Jae Seung, Jeon Jun Ho, Jang Mi Seon, Kang Seok-Seong, Ahn Ki Bum, Song Manki, Yun Cheol-Heui, Han Seung Hyun

机构信息

Clinical Research Laboratory, Sciences Unit, International Vaccine Institute, Seoul, Republic of Korea.

Division of High-Risk Pathogen Research, Center for Infectious Diseases, Korea National Institute of Health, Cheongju, Republic of Korea.

出版信息

Mol Immunol. 2018 Jan;93:47-54. doi: 10.1016/j.molimm.2017.11.005. Epub 2017 Nov 13.

DOI:10.1016/j.molimm.2017.11.005
PMID:29145158
Abstract

Although Vibrio cholerae colonizes the small intestine and induces acute inflammatory responses, less is known about the molecular mechanisms of V. cholerae-induced inflammatory responses in the intestine. We recently reported that OmpU, one of the most abundant outer membrane proteins of V. cholerae, plays an important role in the innate immunity of the whole bacteria. In this study, we evaluated the role of OmpU in induction of IL-8, a representative chemokine that recruits various inflammatory immune cells, in the human intestinal epithelial cell (IEC) line, HT-29. Recombinant OmpU (rOmpU) of V. cholerae induced IL-8 expression at the mRNA and protein levels in a dose- and time-dependent manner. Interestingly, IL-8 was secreted through both apical and basolateral sides of the polarized HT-29 cells upon apical exposure to rOmpU but not upon basolateral exposure. rOmpU-induced IL-8 expression was inhibited by interference of lipid raft formation with nystatin, but not by blocking the formation of clathrin-coated pits with chlorpromazine. In addition, rOmpU-induced IL-8 expression was mediated via ERK1/2 and p38 kinase pathways, but not via JNK signaling pathway. Finally, V. cholerae lacking ompU elicited decreased IL-8 expression and adherence to HT-29 cells compared to the parental strain. Collectively, these results suggest that V. cholerae OmpU might play an important role in intestinal inflammation by inducing IL-8 expression in human IECs.

摘要

尽管霍乱弧菌定殖于小肠并引发急性炎症反应,但关于霍乱弧菌在肠道中诱导炎症反应的分子机制,我们了解得还较少。我们最近报道,霍乱弧菌最丰富的外膜蛋白之一OmpU在整个细菌的固有免疫中发挥重要作用。在本研究中,我们评估了OmpU在人肠上皮细胞系HT-29中诱导白细胞介素-8(IL-8,一种招募各种炎性免疫细胞的代表性趋化因子)的作用。霍乱弧菌的重组OmpU(rOmpU)以剂量和时间依赖性方式诱导IL-8在mRNA和蛋白质水平的表达。有趣的是,在顶端暴露于rOmpU时,IL-8通过极化的HT-29细胞的顶端和基底外侧分泌,但在基底外侧暴露时则不然。用制霉菌素干扰脂筏形成可抑制rOmpU诱导的IL-8表达,但用氯丙嗪阻断网格蛋白包被小窝的形成则不能。此外,rOmpU诱导的IL-8表达是通过ERK1/2和p38激酶途径介导的,而不是通过JNK信号通路。最后,与亲本菌株相比,缺乏ompU的霍乱弧菌引起的IL-8表达和对HT-29细胞的粘附减少。总的来说,这些结果表明霍乱弧菌OmpU可能通过在人肠上皮细胞中诱导IL-8表达而在肠道炎症中发挥重要作用。

相似文献

1
Vibrio cholerae OmpU induces IL-8 expression in human intestinal epithelial cells.霍乱弧菌外膜蛋白U诱导人肠上皮细胞中白细胞介素-8的表达。
Mol Immunol. 2018 Jan;93:47-54. doi: 10.1016/j.molimm.2017.11.005. Epub 2017 Nov 13.
2
IFN-γ renders human intestinal epithelial cells responsive to lipopolysaccharide of Vibrio cholerae by down-regulation of DMBT1.IFN-γ 通过下调 DMBT1 使人类肠道上皮细胞对霍乱弧菌脂多糖产生反应。
Comp Immunol Microbiol Infect Dis. 2012 Jul;35(4):345-54. doi: 10.1016/j.cimid.2012.02.003. Epub 2012 Mar 20.
3
Characterization of the role of the ToxR-modulated outer membrane porins OmpU and OmpT in Vibrio cholerae virulence.霍乱弧菌毒力中ToxR调节的外膜孔蛋白OmpU和OmpT的作用特征
J Bacteriol. 2001 Jun;183(12):3652-62. doi: 10.1128/JB.183.12.3652-3662.2001.
4
Characterization of outer membrane protein OmpU of Vibrio cholerae O1.霍乱弧菌O1型外膜蛋白OmpU的特性分析
Infect Immun. 1998 Oct;66(10):4726-8. doi: 10.1128/IAI.66.10.4726-4728.1998.
5
Vibrio cholerae porin OmpU induces LPS tolerance by attenuating TLR-mediated signaling.霍乱弧菌孔蛋白OmpU通过减弱TLR介导的信号传导诱导脂多糖耐受性。
Mol Immunol. 2015 Dec;68(2 Pt A):312-24. doi: 10.1016/j.molimm.2015.09.021. Epub 2015 Oct 9.
6
The OmpU outer membrane protein, a potential adherence factor of Vibrio cholerae.外膜蛋白OmpU是霍乱弧菌的一种潜在黏附因子。
Infect Immun. 1995 Nov;63(11):4433-8. doi: 10.1128/iai.63.11.4433-4438.1995.
7
Vibrio cholerae porin OmpU mediates M1-polarization of macrophages/monocytes via TLR1/TLR2 activation.霍乱弧菌孔蛋白OmpU通过激活TLR1/TLR2介导巨噬细胞/单核细胞的M1极化。
Immunobiology. 2015 Nov;220(11):1199-209. doi: 10.1016/j.imbio.2015.06.009. Epub 2015 Jun 5.
8
The Vibrio cholerae ToxR-regulated porin OmpU confers resistance to antimicrobial peptides.霍乱弧菌ToxR调控的孔蛋白OmpU赋予对抗菌肽的抗性。
Infect Immun. 2004 Jun;72(6):3577-83. doi: 10.1128/IAI.72.6.3577-3583.2004.
9
Interleukin-8 gene regulation in epithelial cells by Vibrio cholerae: role of multiple promoter elements, adherence and motility of bacteria and host MAPKs.霍乱弧菌调控上皮细胞中白细胞介素-8 基因的表达:多个启动子元件、细菌黏附和运动以及宿主 MAPK 的作用。
FEBS J. 2012 Apr;279(8):1464-73. doi: 10.1111/j.1742-4658.2012.08539.x. Epub 2012 Mar 14.
10
Antimicrobial peptides activate the Vibrio cholerae sigmaE regulon through an OmpU-dependent signalling pathway.抗菌肽通过依赖于外膜蛋白U(OmpU)的信号通路激活霍乱弧菌的σE调节子。
Mol Microbiol. 2007 Feb;63(3):848-58. doi: 10.1111/j.1365-2958.2006.05544.x. Epub 2006 Dec 20.

引用本文的文献

1
Characterization of bacteria colonizing the mucosal layer of the gastrointestinal tract of Atlantic salmon farmed in a warm water region.对在温水区域养殖的大西洋鲑鱼胃肠道粘膜层定殖细菌的特性分析。
Front Microbiol. 2025 Jul 23;16:1564052. doi: 10.3389/fmicb.2025.1564052. eCollection 2025.
2
Secretome of adipose derived-mesenchymal stem cells reduces the attachment to Caco-2 cells and subsequent inflammatory responses.脂肪来源间充质干细胞的分泌组可减少对Caco-2细胞的附着及随后的炎症反应。
Iran J Microbiol. 2024 Feb;16(1):79-89. doi: 10.18502/ijm.v16i1.14875.
3
Outer membrane vesicles and the outer membrane protein OmpU govern biofilm matrix assembly.
外膜囊泡和外膜蛋白 OmpU 控制生物膜基质的组装。
mBio. 2024 Feb 14;15(2):e0330423. doi: 10.1128/mbio.03304-23. Epub 2024 Jan 11.
4
Dynamic Interactions between Diarrhoeagenic Enteroaggregative and Presumptive Probiotic Bacteria: Implications for Gastrointestinal Health.致泻性聚集性大肠杆菌与推定益生菌之间的动态相互作用:对胃肠道健康的影响
Microorganisms. 2023 Dec 8;11(12):2942. doi: 10.3390/microorganisms11122942.
5
, classification, pathogenesis, immune response, and trends in vaccine development.分类、发病机制、免疫反应及疫苗研发趋势。
Front Med (Lausanne). 2023 May 5;10:1155751. doi: 10.3389/fmed.2023.1155751. eCollection 2023.
6
Vibrio cholerae senses human enteric α-defensin 5 through a CarSR two-component system to promote bacterial pathogenicity.霍乱弧菌通过 CarSR 双组分系统感知人体肠道防御素 5,从而促进细菌的致病性。
Commun Biol. 2022 Jun 8;5(1):559. doi: 10.1038/s42003-022-03525-3.
7
Neutrophil-Associated Responses to Vibrio cholerae Infection in a Natural Host Model.天然宿主模型中霍乱弧菌感染相关中性粒细胞反应。
Infect Immun. 2022 Mar 17;90(3):e0046621. doi: 10.1128/iai.00466-21. Epub 2022 Jan 24.
8
Plasmid-Encoded CPSIT_P7 Elicits Inflammatory Response in Human Monocytes via TLR4/Mal/MyD88/NF-κB Signaling Pathway.质粒编码的CPSIT_P7通过TLR4/Mal/MyD88/NF-κB信号通路在人单核细胞中引发炎症反应。
Front Microbiol. 2020 Dec 3;11:578009. doi: 10.3389/fmicb.2020.578009. eCollection 2020.
9
Virulence Regulation and Innate Host Response in the Pathogenicity of .毒力调控与固有宿主反应在致病性中的作用
Front Cell Infect Microbiol. 2020 Sep 30;10:572096. doi: 10.3389/fcimb.2020.572096. eCollection 2020.
10
Characterization of Vibrio cholerae isolates from freshwater sources in northwest Ohio.俄亥俄州西北部淡水源分离的霍乱弧菌的特性研究。
PLoS One. 2020 Sep 3;15(9):e0238438. doi: 10.1371/journal.pone.0238438. eCollection 2020.