The Major Outer Membrane Protein of a Periodontopathogen Induces IFN-β and IFN-Stimulated Genes in Monocytes via Lipid Raft and TANK-Binding Kinase 1/IFN Regulatory Factor-3

被引:11
|
作者
Lee, Sung-Hoon [1 ]
Kim, Joong Su [3 ]
Jun, Hye-Kyoung [1 ]
Lee, Hae-Ri [1 ]
Lee, Daesil [3 ]
Choi, Bong-Kyu [1 ,2 ]
机构
[1] Seoul Natl Univ, Sch Dent, Dept Oral Microbiol & Immunol, Seoul 110749, South Korea
[2] Seoul Natl Univ, Sch Dent, Dent Res Inst, Seoul 110749, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Genome Res Ctr, Taejon, South Korea
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 182卷 / 09期
关键词
GINGIVAL CREVICULAR FLUID; INDUCED CELL ACTIVATION; TREPONEMA-LECITHINOLYTICUM; PORPHYROMONAS-GINGIVALIS; MYCOBACTERIUM-TUBERCULOSIS; INTERFERON RESPONSE; OSTEOCLAST DIFFERENTIATION; EPITHELIAL-CELLS; T-CELLS; INFECTIONS;
D O I
10.4049/jimmunol.0802765
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Surface molecules of pathogens play an important role in stimulating host immune responses. Elucidation of file signaling pathways activated by critical surface molecules in host cells provides insight into the molecular pathogenesis resulting from bacteria-host interactions. MspTL is the most abundant outer membrane protein of Treponema lecithinolyticum, which is associated with periodontitis, and induces expression of a variety of proinflammatory factors. Although bacteria and bacterial components like LPS and flagellin are known to induce IFN-beta, induction by bacterial surface proteins has not been reported. In the present study, we investigated MspTL-mediated activation of signaling pathways stimulating up-regulation of IFN-beta and IFN-stinlulated genes in a human monocytic cell line, THP-1 cells, and primary cultured human gingival fibroblasts. MspTL treatment of the cells induced IFN-beta and the IFN-stimulated genes IFN-gamma-inducible protein-10 (IP-10) and RANTES. A neutralizing anti-IFN-beta Ab significantly reduced the expression of IP-10 and RANTES, as well as STAT-1 activation, which was also induced by MspTL Experiments using specific small interfering RNA showed that mspTL activated TANK-binding kinase 1 (TBK1), but not inducible IKB kinase (IKKi). MspTL also induced dimerization of IFN regulatory factor-3 (IRF-3) and translocation into the nucleus. The lipid rapid-disrupting agents methyl-beta-cyclodextrin, nystatin, and filipin inhibited the MspTL, internalization and cellular responses, demonstrating that lipid raft activation was a prerequisite for MspTL cellular signaling. Our results demonstrate that MspTL, the major outer protein of T. lecithinolyticum, induced IFN-beta expression and subsequent up-regulation of IP-10 and RANTES via TBK1/IRF-3/STAT-1 signaling secondary to lipid raft activation. The Journal of Immunology, 2009, 182: 5823-5835.
引用
收藏
页码:5823 / 5835
页数:13
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