Paradoxical Roles of the MAL/Tirap Adaptor in Pathologies

Front Immunol. 2020 Sep 25:11:569127. doi: 10.3389/fimmu.2020.569127. eCollection 2020.

Abstract

Toll-like receptors (TLRs) are at the forefront of pathogen recognition ensuring host fitness and eliciting protective cellular and humoral responses. Signaling pathways downstream of TLRs are tightly regulated for preventing collateral damage and loss of tolerance toward commensals. To trigger effective intracellular signaling, these receptors require the involvement of adaptor proteins. Among these, Toll/Interleukin-1 receptor domain containing adaptor protein (Tirap or MAL) plays an important role in establishing immune responses. Loss of function of MAL was associated with either disease susceptibility or resistance. These opposite effects reveal paradoxical functions of MAL and their importance in containing infectious or non-infectious diseases. In this review, we summarize the current knowledge on the signaling pathways involving MAL in different pathologies and their impact on inducing protective or non-protective responses.

Keywords: MAL/Tirap; TLRs; chronic diseases; inflammation; signaling pathways.

Publication types

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

MeSH terms

  • Animals
  • Carrier Proteins / metabolism
  • Disease Susceptibility*
  • Endosomes / metabolism
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunity, Innate
  • Immunomodulation
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Protein Binding
  • Proteolysis
  • Receptors, Interleukin-1 / chemistry
  • Receptors, Interleukin-1 / genetics
  • Receptors, Interleukin-1 / metabolism*
  • Signal Transduction*
  • Structure-Activity Relationship
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 4 / metabolism

Substances

  • Carrier Proteins
  • Membrane Glycoproteins
  • Receptors, Interleukin-1
  • TIRAP protein, human
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4