A polymorphic protease-activated receptor 2 (PAR2) displaying reduced sensitivity to trypsin and differential responses to PAR agonists

Citation
Sj. Compton et al., A polymorphic protease-activated receptor 2 (PAR2) displaying reduced sensitivity to trypsin and differential responses to PAR agonists, J BIOL CHEM, 275(50), 2000, pp. 39207-39212
Citations number
40
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
275
Issue
50
Year of publication
2000
Pages
39207 - 39212
Database
ISI
SICI code
0021-9258(200012)275:50<39207:APPR2(>2.0.ZU;2-L
Abstract
Protease-activated receptor 2 (PAR2) is a trypsin-activated member of a fam ily of G-protein-coupled PARs. We have identified a polymorphic form of hum an PARS (PAR(2)F240S) characterized by a phenylalanine to serine mutation a t residue 240 within extracellular loop 2, with allelic frequencies of 0.91 6 (Phe(240)) and 0.084 (Ser(240)) for the wild-type and mutant alleles, res pectively. Elevations in intracellular calcium were measured in permanently transfected cell lines expressing the receptors. PAR(2)F240S displayed a s ignificant reduction in sensitivity toward trypsin (similar to3.7-fold) and the PARS-activating peptides, SLIGKV-NH2 (similar to2.5-fold) and SLIGRL-N H2 (similar to2.8-fold), but an increased sensitivity toward the selective PARS agonist, trans- cinnamoyl-LIGRLO-NH2 (similar to4-fold). Increased sen sitivity was also observed toward the selective PAR-1 agonist, TFLLR-NH2 (s imilar to7-fold), but not to other PAR-1 agonists tested. Furthermore, we f ound that TLIGRL-NH2 and a PAR4-derived peptide, trans-cinnamoyl-YPGKF-NH2, were selective PAR(2)F240S agonists. By introducing the F240S mutation int o rat PARS, we observed shifts in agonist potencies that mirrored the human PAR,F240S, suggesting that Phe240 is involved in determining agonist speci ficity of PARS. Finally, differences in receptor signaling were paralleled in a cell growth assay. We suggest that the distinct pharmacological profil e induced by this polymorphism will have important implications for the des ign of PAR-targeted agonists/antagonists and may contribute to, or be predi ctive of, an inflammatory disease.