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

被引:896
|
作者
Briscoe, CP [1 ]
Tadayyon, M
Andrews, JL
Benson, WG
Chambers, JK
Eilert, MM
Ellis, C
Elshourbagy, NA
Goetz, AS
Minnick, DT
Murdock, PR
Sauls, HR
Shabon, U
Spinage, LD
Strum, JC
Szekeres, PG
Tan, KB
Way, JM
Ignar, DM
Wilson, S
Muir, AI
机构
[1] GlaxoSmithKline, Dept Metab Dis, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline, Dept Syst Res, Res Triangle Pk, NC 27709 USA
[3] GlaxoSmithKline, Dept Genom Histol, Res Triangle Pk, NC 27709 USA
[4] GlaxoSmithKline, Dept Cellular Genom, Res Triangle Pk, NC 27709 USA
[5] GlaxoSmithKline, Dept Cell Physiol, Res Triangle Pk, NC 27709 USA
[6] GlaxoSmithKline, Dept Vasc Biol, Harlow CM19 5AD, Essex, England
[7] GlaxoSmithKline, Dept Syst Res, Harlow CM19 5AD, Essex, England
[8] GlaxoSmithKline, Dept Quantitat Express, Harlow CM19 5AD, Essex, England
[9] GlaxoSmithKline, Dept Gene Cloning, Harlow CM19 5AD, Essex, England
[10] GlaxoSmithKline, Dept Gene Cloning, King Of Prussia, PA 19406 USA
[11] GlaxoSmithKline, Dept Express Genom, King Of Prussia, PA 19406 USA
关键词
D O I
10.1074/jbc.M211495200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 [Ca2+](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 Galpha(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 Galpha(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.
引用
收藏
页码:11303 / 11311
页数:9
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