Leptospiral lipopolysaccharide activates cells through a TLR2-dependent mechanism

被引:556
作者
Werts, C
Tapping, RI
Mathison, JC
Chuang, TH
Kravchenko, V
Saint Girons, I
Haake, DA
Godowski, PJ
Hayashi, F
Ozinsky, A
Underhill, DM
Kirschning, CJ
Wagner, H
Aderem, A
Tobias, PS
Ulevitch, RJ [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] Inst Pasteur, Unite Bacteriol Mol & Med, F-75724 Paris 15, France
[3] Vet Affairs Greater Los Angeles Hlth Care Syst, Div Infect Dis, Los Angeles, CA 90073 USA
[4] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
[5] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[6] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-81675 Munich, Germany
关键词
D O I
10.1038/86354
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Leptospira interrogans are zoonotic pathogens that have been linked to a recent increased incidence of morbidity and mortality in highly populated tropical urban centers. They are unique among invasive spirochetes in that they contain outer membrane lipopolysaccharide (LPS) as well as lipoproteins. Here we show that both these leptospiral outer membrane constituents activate macrophages through CD14 and the Toll-like receptor 2 (TLR2). Conversely, it seems that TLR4, a central component for recognition of Gram-negative LPS, is not involved in cellular responses to L. interrogans. We also show that for intact L. interrogans, it is LPS, not lipoprotein, that constitutes the predominant signaling component for macrophages through a TLR2 pathway. These data provide a basis for understanding the innate immune response caused by leptospirosis and demonstrate a new ligand specificity for TLR2.
引用
收藏
页码:346 / 352
页数:7
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