Yang Jae Seung, Jeon Jun Ho, Jang Mi Seon, Kang Seok-Seong, Ahn Ki Bum, Song Manki, Yun Cheol-Heui, Han Seung Hyun
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.
Mol Immunol. 2018 Jan;93:47-54. doi: 10.1016/j.molimm.2017.11.005. Epub 2017 Nov 13.
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.
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。