Toll-like receptor-2 mediates mycobacteria-induced proinflammatory signaling in macrophages

被引:644
作者
Underhill, DM
Ozinsky, A
Smith, KD
Aderem, A
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
关键词
MyD88; Mycobacterium tuberculosis; tumor necrosis factor alpha;
D O I
10.1073/pnas.96.25.14459
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The recognition of mycobacterial cell wall components causes macrophages to secrete tumor necrosis factor alpha (TNF-alpha) and other cytokines that are essential for the development of a protective inflammatory response. We show that toll-like receptors are required for the induction of TNF-alpha in macrophages by Mycobacterium tuberculosis. Expression of a dominant negative form of MyD88 (9 signaling component required for toll-like receptor signaling) in a mouse macrophage cell line blocks TNF-alpha production induced by M. tuberculosis. We identify toll-like receptor-2 (TLR2) as the specific toll-like receptor required for this induction by showing that expression of an inhibitory TLR2 (TLR2-P681H) blocks TNF-alpha production induced by whole M. tuberculosis. Further. we show that TLR2-dependent signaling mediates responses to mycobacterial cell wall fractions enriched for lipoarrabinomannan. mycolylarabinogalactan-peptidoglycan complex. or M. tuberculosis total lipids. Thus, although many mycobacterial cell wall fractions are identified to be inflammatory, all require TLR2 for induction of TNF-alpha in macrophages. These data suggest that TLR2 is essential for the induction of a protective immune response to mycobacteria.
引用
收藏
页码:14459 / 14463
页数:5
相关论文
共 42 条
  • [31] Peptidoglycan- and lipoteichoic acid-induced cell activation is mediated by toll-like receptor 2
    Schwandner, R
    Dziarski, R
    Wesche, H
    Rothe, M
    Kirschning, CJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (25) : 17406 - 17409
  • [32] TLR6: A novel member of an expanding Toll-like receptor family
    Takeuchi, O
    Kawai, T
    Sanjo, H
    Copeland, NG
    Gilbert, DJ
    Jenkins, NA
    Takeda, K
    Akira, S
    [J]. GENE, 1999, 231 (1-2) : 59 - 65
  • [33] Recognition of Gram-negative bacteria and endotoxin by the innate immune system
    Ulevitch, RJ
    Tobias, PS
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (01) : 19 - 22
  • [34] MacMARCKS is not essential for phagocytosis in macrophages
    Underhill, DM
    Chen, JM
    Allen, LAH
    Aderem, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (50) : 33619 - 33623
  • [35] The Toll-like receptor 2 is recruited to macrophage phagosomes and discriminates between pathogens
    Underhill, DM
    Ozinsky, A
    Hajjar, AM
    Stevens, A
    Wilson, CB
    Bassetti, M
    Aderem, A
    [J]. NATURE, 1999, 401 (6755) : 811 - 815
  • [36] Phosphatidylinositides bind to plasma membrane CD14 and can prevent monocyte activation by bacterial lipopolysaccharide
    Wang, PY
    Kitchens, RL
    Munford, RS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (38) : 24309 - 24313
  • [37] MyD88: An adapter that recruits IRAK to the IL-1 receptor complex
    Wesche, H
    Henzel, WJ
    Shillinglaw, W
    Li, S
    Cao, ZD
    [J]. IMMUNITY, 1997, 7 (06) : 837 - 847
  • [38] Toll-like receptor-2 mediates lipopolysaccharide-induced cellular signalling
    Yang, RB
    Mark, MR
    Gray, A
    Huang, A
    Xie, MH
    Zhang, M
    Goddard, A
    Wood, WI
    Gurney, AL
    Godowski, PJ
    [J]. NATURE, 1998, 395 (6699) : 284 - 288
  • [39] Yoshimura A, 1999, J IMMUNOL, V163, P1
  • [40] Lipopolysaccharide binding protein and soluble CD14 catalyze exchange of phospholipids
    Yu, B
    Hailman, E
    Wright, SD
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (02) : 315 - 324