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

Proc Natl Acad Sci U S A. 1999 Dec 7;96(25):14459-63. doi: 10.1073/pnas.96.25.14459.

Abstract

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 (a 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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, Differentiation / physiology
  • Cell Line
  • Drosophila Proteins*
  • Lipopolysaccharides / metabolism
  • Macrophages / immunology*
  • Membrane Glycoproteins / physiology*
  • Mice
  • Mycobacterium tuberculosis / immunology*
  • Myeloid Differentiation Factor 88
  • NF-kappa B / metabolism
  • Peptidoglycan / metabolism
  • Receptors, Cell Surface / physiology*
  • Receptors, Immunologic*
  • Toll-Like Receptor 2
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • Drosophila Proteins
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Peptidoglycan
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Toll-Like Receptor 2
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha
  • lipoarabinomannan