Toll-like receptor signaling pathways

Science. 2003 Jun 6;300(5625):1524-5. doi: 10.1126/science.1085536.

Abstract

Members of the Toll-like receptor (TLR) family recognize conserved microbial structures, such as bacterial lipopolysaccharide and viral double-stranded RNA, and activate signaling pathways that result in immune responses against microbial infections. All TLRs activate MyD88-dependent pathways to induce a core set of stereotyped responses, such as inflammation. However, individual TLRs can also induce immune responses that are tailored to a given microbial infection. Thus, these receptors are involved in both innate and adaptive immune responses. The mechanisms and components of these varied responses are only partly understood. Given the importance of TLRs in host defense, dissection of the pathways they activate has become an important emerging research focus. TLRs and their pathways are numerous; Science's Signal Transduction Knowledge Environment's TLR Connections Map provides an immediate, clear overview of the known components and relations of this complex system.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Antigens, Differentiation / metabolism
  • Immunity, Active*
  • Immunity, Innate*
  • Infections / immunology*
  • Infections / metabolism
  • Inflammation
  • Interleukin-1 Receptor-Associated Kinases
  • MAP Kinase Signaling System
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Myeloid Differentiation Factor 88
  • NF-kappa B / metabolism
  • Protein Kinases / metabolism
  • Protein Structure, Tertiary
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / metabolism*
  • Receptors, Immunologic / metabolism
  • Signal Transduction*
  • Toll-Like Receptors

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • Membrane Glycoproteins
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Toll-Like Receptors
  • Protein Kinases
  • Interleukin-1 Receptor-Associated Kinases
  • Mitogen-Activated Protein Kinases