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淋病奈瑟菌的脂蛋白以Toll样受体2依赖的方式刺激上皮细胞释放细胞因子并激活核因子κB。

The Lip lipoprotein from Neisseria gonorrhoeae stimulates cytokine release and NF-kappaB activation in epithelial cells in a Toll-like receptor 2-dependent manner.

作者信息

Fisette Philip L, Ram Sanjay, Andersen Jorunn M, Guo Wen, Ingalls Robin R

机构信息

Division of Infectious Diseases, Department of Physiology and Biophysics, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA.

出版信息

J Biol Chem. 2003 Nov 21;278(47):46252-60. doi: 10.1074/jbc.M306587200. Epub 2003 Sep 9.

Abstract

The human pathogen Neisseria gonorrhoeae produces an array of diseases ranging from urethritis to disseminated gonococcal infections. Early events in the establishment of infection involve interactions between N. gonorrhoeae and the mucosal epithelium, which leads to the local release of inflammatory mediators. Because of this, it is important to identify the bacterial virulence factors and host cell components that contribute to inflammation. Using a series of column chromatography steps, we purified a lipoprotein from N. gonorrhoeae strain F62 called Lip. This outer membrane antigen expresses a conserved epitope known as H.8, which is common to all pathogenic Neisseria species. We found the purified preparation of Lip to be a potent inflammatory mediator capable of inducing the release of the chemokine interleukin (IL)-8 and the cytokine IL-6 by immortalized human endocervical epithelial cells and the production of IL-8 and the activation of the transcription factor NF-kappaB by human embryonic kidney 293 (HEK) cells transfected with toll-like receptor (TLR) 2. Upon removal of Lip by immunoprecipitation, the ability of the H.8/Lip preparation to stimulate NF-kappaB activation was abolished. In addition to TLR2, the activation of NF-kappaB by H.8/Lip in HEK cells was enhanced upon coexpression of TLR1 but not TLR6. These observations provide evidence that Lip is capable of inducing the release of inflammatory mediators from epithelial cells in a TLR2-dependent manner.

摘要

人类病原体淋病奈瑟菌可引发一系列疾病,从尿道炎到播散性淋球菌感染。感染初期事件涉及淋病奈瑟菌与黏膜上皮之间的相互作用,这会导致炎症介质在局部释放。因此,识别促成炎症的细菌毒力因子和宿主细胞成分很重要。通过一系列柱层析步骤,我们从淋病奈瑟菌F62菌株中纯化出一种名为Lip的脂蛋白。这种外膜抗原表达一种名为H.8的保守表位,所有致病性奈瑟菌属物种都有该表位。我们发现纯化后的Lip制剂是一种强效炎症介质,能够诱导永生化人宫颈上皮细胞释放趋化因子白细胞介素(IL)-8和细胞因子IL-6,并能诱导转染了Toll样受体(TLR)2的人胚肾293(HEK)细胞产生IL-8以及激活转录因子核因子κB。通过免疫沉淀去除Lip后,H.8/Lip制剂刺激核因子κB激活的能力就被消除了。除了TLR2外,在HEK细胞中,H.8/Lip与TLR1共表达时,其激活核因子κB的能力增强,但与TLR6共表达时则不然。这些观察结果证明,Lip能够以TLR2依赖的方式诱导上皮细胞释放炎症介质。

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