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表皮葡萄球菌胞间多糖黏附素通过涉及Toll样受体2(TLR2)的机制诱导人星形胶质细胞表达白细胞介素-8(IL-8)。

Staphylococcus epidermidis polysaccharide intercellular adhesin induces IL-8 expression in human astrocytes via a mechanism involving TLR2.

作者信息

Stevens Niall T, Sadovskaya Irina, Jabbouri Said, Sattar Tafiq, O'Gara James P, Humphreys Hilary, Greene Catherine M

机构信息

Department of Clinical Microbiology, Royal College of Surgeons in Ireland Education & Research Centre, Beaumont Hospital, Dublin, Ireland.

出版信息

Cell Microbiol. 2009 Mar;11(3):421-32. doi: 10.1111/j.1462-5822.2008.01264.x. Epub 2008 Nov 7.

DOI:10.1111/j.1462-5822.2008.01264.x
PMID:19016779
Abstract

Staphylococcus epidermidis is an opportunistic biofilm-forming pathogen associated with neurosurgical device-related meningitis. Expression of the polysaccharide intercellular adhesin (PIA) on its surface promotes S. epidermidis biofilm formation. Here we investigated the pro-inflammatory properties of PIA against primary and transformed human astrocytes. PIA induced IL-8 expression in a dose- and/or time-dependent manner from U373 MG cells and primary normal human astrocytes. This effect was inhibited by depletion of N-acetyl-beta-d-glucosamine polymer from the PIA preparation with Lycopersicon esculentum lectin or sodium meta-periodate. Expression of dominant-negative versions of the TLR2 and TLR4 adaptor proteins MyD88 and Mal in U373 MG cells inhibited PIA-induced IL-8 production. Blocking IL-1 had no effect. PIA failed to induce IL-8 production from HEK293 cells stably expressing TLR4. However, in U373 MG cells which express TLR2, neutralization of TLR2 impaired PIA-induced IL-8 production. In addition to IL-8, PIA also induced expression of other cytokines from U373 MG cells including IL-6 and MCP-1. These data implicate PIA as an important immunogenic component of the S. epidermidis biofilm that can regulate pro-inflammatory cytokine production from human astrocytes, in part, via TLR2.

摘要

表皮葡萄球菌是一种与神经外科器械相关脑膜炎有关的机会性生物膜形成病原体。其表面多糖细胞间黏附素(PIA)的表达促进表皮葡萄球菌生物膜的形成。在此,我们研究了PIA对原代和转化人星形胶质细胞的促炎特性。PIA以剂量和/或时间依赖性方式诱导U373 MG细胞和原代正常人星形胶质细胞表达IL-8。用番茄凝集素或偏高碘酸钠从PIA制剂中去除N-乙酰-β-D-葡萄糖胺聚合物可抑制这种效应。在U373 MG细胞中表达TLR2和TLR4衔接蛋白MyD88和Mal的显性负性变体可抑制PIA诱导的IL-8产生。阻断IL-1没有效果。PIA不能诱导稳定表达TLR4的HEK293细胞产生IL-8。然而,在表达TLR2的U373 MG细胞中,中和TLR2会损害PIA诱导的IL-8产生。除了IL-8,PIA还诱导U373 MG细胞表达包括IL-6和MCP-1在内的其他细胞因子。这些数据表明PIA是表皮葡萄球菌生物膜的一种重要免疫原性成分,它可以部分通过TLR2调节人星形胶质细胞促炎细胞因子的产生。

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