TLR Signaling

Cell Death Differ. 2006 May;13(5):816-25. doi: 10.1038/sj.cdd.4401850.

Abstract

The Toll-like receptor (TLR) family plays an instructive role in innate immune responses against microbial pathogens, as well as the subsequent induction of adaptive immune responses. TLRs recognize specific molecular patterns found in a broad range of microbial pathogens such as bacteria and viruses, triggering inflammatory and antiviral responses and dendritic cell maturation, which result in the eradication of invading pathogens. Individual TLRs interact with different combinations of adapter proteins and activate various transcription factors such as nuclear factor (NF)-kappaB, activating protein-1 and interferon regulatory factors, driving a specific immune response. This review outlines the recent advances in our understanding of TLR-signaling pathways and their roles in immune responses. Further, we also discuss a new concept of TLR-independent mechanisms for recognition of microbial pathogens.

Publication types

  • Review

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • DEAD-box RNA Helicases
  • Drosophila
  • Gene Expression Regulation*
  • Humans
  • Immunity, Innate*
  • Interferon Regulatory Factors / metabolism
  • Interferon-Induced Helicase, IFIH1
  • Membrane Proteins / metabolism
  • Mice
  • Models, Biological
  • Myeloid Differentiation Factor 88
  • NF-kappa B / metabolism
  • Nerve Tissue Proteins / metabolism
  • RNA Helicases / metabolism
  • Signal Transduction*
  • Toll-Like Receptors / metabolism*
  • Transcription Factor AP-1 / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport
  • Interferon Regulatory Factors
  • MYD88 protein, human
  • Membrane Proteins
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • NF-kappa B
  • Nerve Tissue Proteins
  • Robo3 protein, mouse
  • Toll-Like Receptors
  • Transcription Factor AP-1
  • IFIH1 protein, human
  • DEAD-box RNA Helicases
  • Interferon-Induced Helicase, IFIH1
  • RNA Helicases