PAR-2 regulates dental pulp inflammation associated with caries

J Dent Res. 2010 Jul;89(7):684-8. doi: 10.1177/0022034510365652. Epub 2010 May 26.

Abstract

Protease-activated receptors (PARs) are G-protein-coupled receptors that are activated enzymatically by proteolysis of an N-terminal domain. The cleavage and activation of PARs by serine proteases represent a novel mechanism by which such enzymes could influence the host inflammatory response. The aim of this study was to determine whether PAR-2 expression and activation were increased in dental caries. Using immunohistochemistry, we showed PAR-2 to be localized to pulp cells subjacent to caries lesions, but minimally expressed by healthy pulp tissue. Trypsin and the PAR-2 agonist (PAR2-AP) activated PAR-2 in an in vitro functional assay. Endogenous molecules present in pulp cell lysates from carious teeth specifically activated PAR-2, but those from healthy teeth failed to do so. The activation of PAR-2 in vitro was shown to increase the expression of the pro-inflammatory mediator cyclo-oxygenase-2 (COX-2), providing a mechanism whereby PAR-2 could modulate pulpal inflammation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Calcium / analysis
  • Cells, Cultured
  • Cyclooxygenase 2 / analysis
  • Dental Caries / metabolism*
  • Dental Caries / pathology
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Activation
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Humans
  • Immunohistochemistry
  • Inflammation Mediators / analysis
  • Pulpitis / metabolism*
  • Pulpitis / pathology
  • Receptor, PAR-2 / agonists
  • Receptor, PAR-2 / analysis*
  • Trypsin / pharmacology

Substances

  • Inflammation Mediators
  • Receptor, PAR-2
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Trypsin
  • Calcium