NF-kappaB is a negative regulator of IL-1beta secretion as revealed by genetic and pharmacological inhibition of IKKbeta

Cell. 2007 Sep 7;130(5):918-31. doi: 10.1016/j.cell.2007.07.009.

Abstract

IKKbeta-dependent NF-kappaB activation plays a key role in innate immunity and inflammation, and inhibition of IKKbeta has been considered as a likely anti-inflammatory therapy. Surprisingly, however, mice with a targeted IKKbeta deletion in myeloid cells are more susceptible to endotoxin-induced shock than control mice. Increased endotoxin susceptibility is associated with elevated plasma IL-1beta as a result of increased pro-IL-1beta processing, which was also seen upon bacterial infection. In macrophages enhanced pro-IL-1beta processing depends on caspase-1, whose activation is inhibited by NF-kappaB-dependent gene products. In neutrophils, however, IL-1beta secretion is caspase-1 independent and depends on serine proteases, whose activity is also inhibited by NF-kappaB gene products. Prolonged pharmacologic inhibition of IKKbeta also augments IL-1beta secretion upon endotoxin challenge. These results unravel an unanticipated role for IKKbeta-dependent NF-kappaB signaling in the negative control of IL-1beta production and highlight potential complications of long-term IKKbeta inhibition.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Carbolines / pharmacology
  • Caspase 1 / metabolism
  • Cell Line
  • Disease Models, Animal
  • Humans
  • I-kappa B Kinase / antagonists & inhibitors
  • I-kappa B Kinase / genetics
  • I-kappa B Kinase / metabolism*
  • Interleukin-1beta / blood
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism*
  • Interleukin-6 / blood
  • Lipopolysaccharides
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Mice
  • Mice, Knockout
  • NF-kappa B / metabolism*
  • Neutrophil Infiltration*
  • Neutrophils / drug effects
  • Neutrophils / enzymology
  • Neutrophils / immunology
  • Neutrophils / metabolism*
  • Neutrophils / pathology
  • Niacinamide / analogs & derivatives
  • Niacinamide / pharmacology
  • Protein Kinase Inhibitors / pharmacology
  • RNA, Messenger / metabolism
  • Receptors, Interleukin-1 / metabolism
  • Serine Endopeptidases / metabolism
  • Serpins / metabolism
  • Shock, Septic / chemically induced
  • Shock, Septic / enzymology
  • Shock, Septic / immunology
  • Shock, Septic / metabolism*
  • Shock, Septic / pathology
  • Time Factors
  • Transfection
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Carbolines
  • Interleukin-1beta
  • Interleukin-6
  • Lipopolysaccharides
  • N-(6-chloro-7-methoxy-9H-beta-carbolin-8-yl)-2-methylnicotinamide
  • NF-kappa B
  • Protein Kinase Inhibitors
  • RNA, Messenger
  • Receptors, Interleukin-1
  • Serpins
  • Tumor Necrosis Factor-alpha
  • lipopolysaccharide, Escherichia coli O111 B4
  • Niacinamide
  • I-kappa B Kinase
  • Serine Endopeptidases
  • Caspase 1