HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The orphan receptor GPR17 identified as a new dual uracil nucleotides/cysteinyl-leukotrienes receptor.

Abstract
Nucleotides and cysteinyl-leukotrienes (CysLTs) are unrelated signaling molecules inducing multiple effects through separate G-protein-coupled receptors: the P2Y and the CysLT receptors. Here we show that GPR17, a Gi-coupled orphan receptor at intermediate phylogenetic position between P2Y and CysLT receptors, is specifically activated by both families of endogenous ligands, leading to both adenylyl cyclase inhibition and intracellular calcium increases. Agonist-response profile, as determined by [(35)S]GTPgammaS binding, was different from that of already known CysLT and P2Y receptors, with EC(50) values in the nanomolar and micromolar range, for CysLTs and uracil nucleotides, respectively. Both rat and human receptors are highly expressed in the organs typically undergoing ischemic damage, that is, brain, heart and kidney. In vivo inhibition of GPR17 by either CysLT/P2Y receptor antagonists or antisense technology dramatically reduced ischemic damage in a rat focal ischemia model, suggesting GPR17 as the common molecular target mediating brain damage by nucleotides and CysLTs. In conclusion, the deorphanization of GPR17 revealed a dualistic receptor for two endogenous unrelated ligand families. These findings may lead to dualistic drugs of previously unexplored therapeutic potential.
AuthorsPaolo Ciana, Marta Fumagalli, Maria Letizia Trincavelli, Claudia Verderio, Patrizia Rosa, Davide Lecca, Silvia Ferrario, Chiara Parravicini, Valérie Capra, Paolo Gelosa, Uliano Guerrini, Silvia Belcredito, Mauro Cimino, Luigi Sironi, Elena Tremoli, G Enrico Rovati, Claudia Martini, Maria P Abbracchio
JournalThe EMBO journal (EMBO J) Vol. 25 Issue 19 Pg. 4615-27 (Oct 04 2006) ISSN: 0261-4189 [Print] England
PMID16990797 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • GPR17 protein, human
  • GPR17 protein, rat
  • Leukotrienes
  • Membrane Proteins
  • Receptors, G-Protein-Coupled
  • Receptors, Leukotriene
  • Receptors, Purinergic P2
  • Uracil Nucleotides
  • cysteinyl-leukotriene
  • Cysteine
  • leukotriene D4 receptor
Topics
  • Amino Acid Sequence
  • Animals
  • Brain (cytology, metabolism, pathology)
  • Brain Ischemia (chemically induced)
  • COS Cells
  • Chlorocebus aethiops
  • Cysteine (metabolism)
  • Gene Expression Profiling
  • Humans
  • Leukotrienes (metabolism)
  • Male
  • Membrane Proteins (metabolism)
  • Mice
  • Molecular Sequence Data
  • Neurons (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, G-Protein-Coupled (chemistry, metabolism)
  • Receptors, Leukotriene (metabolism)
  • Receptors, Purinergic P2 (metabolism)
  • Sequence Analysis, Protein
  • Uracil Nucleotides (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: