1. Academic Validation
  2. The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acids

The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acids

  • J Biol Chem. 2003 Mar 28;278(13):11303-11. doi: 10.1074/jbc.M211495200.
Celia P Briscoe 1 Mohammad Tadayyon John L Andrews William G Benson Jon K Chambers Michelle M Eilert Catherine Ellis Nabil A Elshourbagy Aaron S Goetz Dana T Minnick Paul R Murdock Howard R Sauls Jr Usman Shabon Lisa D Spinage Jay C Strum Philip G Szekeres Kong B Tan James M Way Diane M Ignar Shelagh Wilson Alison I Muir
Affiliations

Affiliation

  • 1 Department of Metabolic Diseases, GlaxoSmithKline, Research Triangle Park, North Carolina 27709, USA. [email protected]
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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