The Orphan G Protein-coupled Receptor GPR40 Is Activated by Medium and Long Chain Fatty Acids

Celia P. Briscoe(Research Triangle Park Foundation), Mohammad Tadayyon(Center for Vascular Biology Research), John L. Andrews, William G. Benson(Center for Genomic Science), Jon Chambers(Center for Vascular Biology Research), Michelle M. Eilert, Catherine Ellis(Gene Therapy Laboratory), Nabil A. Elshourbagy(GlaxoSmithKline (United Kingdom)), Aaron S. Goetz(Systems Research Institute), Dana T. Minnick, Paul R. Murdock, Howard R. Sauls(Systems Research Institute), Usman Shabon(GlaxoSmithKline (United Kingdom)), Lisa D. Spinage(Center for Vascular Biology Research), Jay C. Strum(Genomics (United Kingdom)), Philip Szekeres(Systems Research Institute), K. B. Tan(GlaxoSmithKline (United Kingdom)), James M. Way(Research Triangle Park Foundation), Diane M. Ignar, Shelagh Wilson(Systems Research Institute), Alison I. Muir(Systems Research Institute)
Journal of Biological Chemistry
March 1, 2003
Cited by 1,098Open Access
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Abstract

GPR40 is a member of a subfamily of homologous G protein-coupled receptors that include GPR41 and GPR43 and that have no current function or ligand ascribed. Ligand fishing experiments in HEK293 cells expressing human GPR40 revealed that a range of saturated and unsaturated carboxylic acids with carbon chain lengths greater than six were able to induce an elevation of [Ca(2+)](i), measured using a fluorometric imaging plate reader. 5,8,11-Eicosatriynoic acid was the most potent fatty acid tested, with a pEC(50) of 5.7. G protein coupling of GPR40 was examined in Chinese hamster ovary cells expressing the G alpha(q/i)-responsive Gal4-Elk1 reporter system. Expression of human GPR40 led to a constitutive induction of luciferase activity, which was further increased by exposure of the cells to eicosatriynoic acid. Neither the constitutive nor ligand-mediated luciferase induction was inhibited by pertussis toxin treatment, suggesting that GPR40 was coupled to G alpha(q/11.) Expression analysis by quantitative reverse transcription-PCR showed that GPR40 was specifically expressed in brain and pancreas, with expression in rodent pancreas being localized to insulin-producing beta-cells. These data suggest that some of the physiological effects of fatty acids in pancreatic islets and brain may be mediated through a cell-surface receptor.


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