Activation of protease-activated receptor-2 (PAR-2) triggers mucin secretion in the rat sublingual gland

Biochem Biophys Res Commun. 2000 Apr 2;270(1):298-302. doi: 10.1006/bbrc.2000.2404.

Abstract

Protease-activated receptor-2 (PAR-2) is distributed throughout the gastrointestinal systems. The present study investigated the role for PAR-2 in the rat salivary glands. PAR-2 mRNA was detected in the sublingual, submaxillary, and parotid glands by a reverse-transcriptase polymerase chain reaction. In the isolated sublingual gland that exhibited the strongest signal for PAR-2, Ser-Leu-Ile-Gly-Arg-Leu-NH(2), a PAR-2-activating peptide, and trypsin, a PAR-2-activating enzyme, but not thrombin that can activate PARs 1, 3, and 4, triggered secretion of N-acetylneuraminic acid, an indicator of mucin, that was a unique major sialic acid detectable after hydrolysis of the sublingual mucin with 0.1 N HCl. The PAR-2-mediated secretion of mucin was attenuated by genistein, a tyrosine kinase inhibitor, but not by inhibitors of protein kinase C and phosphatidyl inositol 3'-kinase. Thus, PAR-2 is expressed by the three distinct salivary glands in the rat, and sublingual PAR-2 appears to play a role in triggering mucin secretion, at least in part, via activation of tyrosine kinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Genistein / pharmacology
  • In Vitro Techniques
  • Male
  • Mucins / metabolism*
  • Oligopeptides / pharmacology
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Kinase C / antagonists & inhibitors
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Rats
  • Rats, Wistar
  • Receptor, PAR-2
  • Receptors, Thrombin / agonists
  • Receptors, Thrombin / metabolism*
  • Sialic Acids / metabolism
  • Sublingual Gland / metabolism*

Substances

  • Mucins
  • Oligopeptides
  • Phosphoinositide-3 Kinase Inhibitors
  • Receptor, PAR-2
  • Receptors, Thrombin
  • Sialic Acids
  • seryl-leucyl-isoleucyl-glycyl-arginyl-leucine
  • Genistein
  • Protein-Tyrosine Kinases
  • Protein Kinase C