Caspase-1 is involved in the genesis of inflammatory hypernociception by contributing to peripheral IL-1β maturation

Mol Pain. 2010 Oct 4:6:63. doi: 10.1186/1744-8069-6-63.

Abstract

Background: Caspase-1 is a cysteine protease responsible for the processing and secretion of IL-1β and IL-18, which are closely related to the induction of inflammation. However, limited evidence addresses the participation of caspase-1 in inflammatory pain. Here, we investigated the role of caspase-1 in inflammatory hypernociception (a decrease in the nociceptive threshold) using caspase-1 deficient mice (casp1-/-).

Results: Mechanical inflammatory hypernociception was evaluated using an electronic version of the von Frey test. The production of cytokines, PGE₂ and neutrophil migration were evaluated by ELISA, radioimmunoassay and myeloperoxidase activity, respectively. The interleukin (IL)-1β and cyclooxygenase (COX)-2 protein expression were evaluated by western blotting. The mechanical hypernociception induced by intraplantar injection of carrageenin, tumour necrosis factor (TNF)α and CXCL1/KC was reduced in casp1-/- mice compared with WT mice. However, the hypernociception induced by IL-1β and PGE₂ did not differ in WT and casp1-/- mice. Carrageenin-induced TNF-α and CXCL1/KC production and neutrophil recruitment in the paws of WT mice were not different from casp1-/- mice, while the maturation of IL-1β was reduced in casp1-/- mice. Furthermore, carrageenin induced an increase in the expression of COX-2 and PGE₂ production in the paw of WT mice, but was reduced in casp1-/- mice.

Conclusion: These results suggest that caspase-1 plays a critical role in the cascade of events involved in the genesis of inflammatory hypernociception by promoting IL-1β maturation. Because caspase-1 is involved in the induction of COX-2 expression and PGE₂ production, our data support the assertion that caspase-1 is a key target to control inflammatory pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caspase 1 / metabolism*
  • Chemokine CXCL1 / metabolism
  • Cyclooxygenase 2 / biosynthesis
  • Dinoprostone / biosynthesis
  • Enzyme Induction
  • Inflammation / enzymology*
  • Inflammation / pathology*
  • Interleukin-18 / metabolism
  • Interleukin-1beta / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neutrophils / metabolism
  • Nociceptors / enzymology*
  • Nociceptors / pathology
  • Protein Processing, Post-Translational*
  • Tumor Necrosis Factor-alpha

Substances

  • Chemokine CXCL1
  • Interleukin-18
  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Caspase 1
  • Dinoprostone