A key role for redox signaling in rapid P2X7 receptor-induced IL-1 beta processing in human monocytes

J Immunol. 2008 Jun 15;180(12):8410-20. doi: 10.4049/jimmunol.180.12.8410.

Abstract

P2X(7) receptors (P2X(7)Rs) are ATP-gated ion channels that trigger caspase-1 activation in the presence of TLR ligands. Inflammatory caspase-1 is responsible for the proteolytic activation of IL-1beta. However, the signaling events that couple P2X(7)Rs to caspase-1 activation remain undefined. In this study we demonstrate that ATP-induced cellular oxidation is critical for caspase-1 activation and subsequent IL-1beta processing. Purinergic receptor stimulation, including P2X(7)Rs, of endotoxin-primed human monocytes augments NADPH oxidase activity whereas concurrent purinergic receptor stimulation triggers protein denitroyslation, leading to the formation of peroxynitrite. IL-1beta cleavage is blocked under conditions where superoxide anion formation is blocked or monocytes are treated with antioxidants or a peroxynitrite scavenger. Nigericin, a K(+)/H(+) antiporter, also increases NADPH oxidase activity, leading to IL-1beta and caspase-1 processing that is blocked by a peroxynitrite scavenger or inhibition of NADPH oxidase. These data demonstrate that signaling via NADPH oxidase activity is fundamental for the processing of mature IL-1beta induced by P2X(7)R stimulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / physiology
  • Caspase 1 / chemistry
  • Caspase 1 / metabolism
  • Cell Line, Tumor
  • Enzyme Activation / immunology
  • Extracellular Fluid / enzymology
  • Extracellular Fluid / immunology
  • Extracellular Fluid / metabolism
  • Humans
  • Interleukin-1beta / antagonists & inhibitors
  • Interleukin-1beta / chemistry
  • Interleukin-1beta / metabolism*
  • Ion Channel Gating / immunology
  • Monocytes / enzymology
  • Monocytes / immunology*
  • Monocytes / metabolism*
  • NADPH Oxidases / antagonists & inhibitors
  • NADPH Oxidases / metabolism
  • NADPH Oxidases / physiology
  • Nitric Oxide / chemistry
  • Nitric Oxide / metabolism
  • Oxidants / physiology
  • Oxidation-Reduction
  • Protein Processing, Post-Translational / immunology*
  • Receptors, Purinergic P2 / chemistry*
  • Receptors, Purinergic P2 / physiology*
  • Receptors, Purinergic P2X7
  • S-Nitrosothiols / chemistry
  • S-Nitrosothiols / metabolism
  • Signal Transduction / immunology*

Substances

  • Interleukin-1beta
  • Oxidants
  • P2RX7 protein, human
  • Receptors, Purinergic P2
  • Receptors, Purinergic P2X7
  • S-Nitrosothiols
  • Nitric Oxide
  • Adenosine Triphosphate
  • NADPH Oxidases
  • Caspase 1