NLRC5 negatively regulates the NF-kappaB and type I interferon signaling pathways

Cell. 2010 Apr 30;141(3):483-96. doi: 10.1016/j.cell.2010.03.040.

Abstract

Stringent control of the NF-kappaB and type I interferon signaling pathways is critical to effective host immune responses, yet the molecular mechanisms that negatively regulate these pathways are poorly understood. Here, we show that NLRC5, a member of the highly conserved NOD-like protein family, can inhibit the IKK complex and RIG-I/MDA5 function. NLRC5 inhibited NF-kappaB-dependent responses by interacting with IKKalpha and IKKbeta and blocking their phosphorylation. It also interacted with RIG-I and MDA5, but not with MAVS, to inhibit RLR-mediated type I interferon responses. Consistent with these observations, NLRC5-specific siRNA knockdown not only enhanced the activation of NF-kappaB and its responsive genes, TNF-alpha and IL-6, but also promoted type I interferon signaling and antiviral immunity. Our findings identify NLRC5 as a negative regulator that blocks two central components of the NF-kappaB and type I interferon signaling pathways and suggest an important role for NLRC5 in homeostatic control of innate immunity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cloning, Molecular
  • DEAD-box RNA Helicases / metabolism
  • Humans
  • I-kappa B Kinase / metabolism
  • Immunity, Innate*
  • Inflammation
  • Interferon Type I / metabolism*
  • Intracellular Signaling Peptides and Proteins / chemistry
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Ligands
  • Mice
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Signal Transduction*
  • Toll-Like Receptors / metabolism

Substances

  • Interferon Type I
  • Intracellular Signaling Peptides and Proteins
  • Ligands
  • NF-kappa B
  • NLRC5 protein, human
  • NLRC5 protein, mouse
  • Toll-Like Receptors
  • I-kappa B Kinase
  • DEAD-box RNA Helicases