Regulation of IRAK-1 activation by its C-terminal domain

Cell Signal. 2009 May;21(5):719-26. doi: 10.1016/j.cellsig.2009.01.010. Epub 2009 Jan 7.

Abstract

Macrophages are important mediators of the immune response to infection by virtue of their ability to secrete cytokines that trigger inflammation. Toll-like receptors (TLRs) are largely responsible for meditating the activation of macrophages by pathogens. IRAK-1 is a proximal protein kinase in TLR signalling pathways and hence its activation must be tightly regulated. However, the mechanisms which control the activation of IRAK-1 are poorly understood. IRAK-1 contains a death domain at its N-terminus that mediates its interaction with other death domain containing proteins, a central Ser/Thr kinase domain, and a C-terminal domain that contains binding motifs for TRAF6. We show here that deletion of the death domain or the majority of the C-terminal domain markedly enhanced the capacity of IRAK-1 to activate NF-kappaB in a TLR-independent manner in RAW 264.7 macrophages. Furthermore, the C-terminal truncation mutant spontaneously oligomerised and formed complexes with the negative regulator IRAK-M in the absence of TLR activation. In contrast to the binding of IRAK-M to IRAK-1, the death domain of IRAK-1 was not required for the interaction of IRAK-4 with IRAK-1. On the basis of these results we propose a model in which IRAK-1 is held in a closed, inactive conformation via an intramolecular mechanism involving its C-terminal domain and possibly the death domain. Phosphorylation of IRAK-1 by IRAK-4 in response to TLR activation may then release IRAK-1 from the inhibitory constraint exerted by its C-terminal domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Gene Expression Regulation
  • Humans
  • Interleukin-1 Receptor-Associated Kinases / chemistry*
  • Interleukin-1 Receptor-Associated Kinases / metabolism*
  • Macrophages / immunology
  • Mice
  • Models, Biological
  • NF-kappa B / metabolism
  • Phosphorylation
  • Protein Structure, Tertiary
  • Sequence Deletion
  • Signal Transduction
  • TNF Receptor-Associated Factor 6 / metabolism
  • Toll-Like Receptors / metabolism*

Substances

  • NF-kappa B
  • TNF Receptor-Associated Factor 6
  • Toll-Like Receptors
  • Interleukin-1 Receptor-Associated Kinases
  • Irak3 protein, mouse