The G-protein-coupled receptor 40 family (GPR40-GPR43) and its role in nutrient sensing

被引:121
作者
Covington, D. K.
Briscoe, C. A.
Brown, A. J.
Jayawickreme, C. K.
机构
[1] GlaxoSmithKline Inc, Dept Mol Pharmacol, Res Triangle Pk, NC 27709 USA
[2] Pfizer, Diabet Biol Dept, San Diego, CA 92121 USA
[3] GlaxoSmithKline Inc, Dept Screening & Compound Profiling, Harlow CM19 5AW, Essex, England
[4] GlaxoSmithKline Inc, Dept Screening & Compound Profiling, Res Triangle Pk, NC 27709 USA
关键词
diabetes; fatty acid; G-protein-coupled receptor; GPR40; family; nutrient sensing; obesity;
D O I
10.1042/BST0340770
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Recent deorphanization efforts have paired the G-protein-coupled receptors GPR40, GPR41 and GPR43 with fatty acids as endogenous ligands. While carboxylic acids have been historically known to serve as fuel sources and biomarkers of disease, these studies demonstrate that fatty acids can act as signalling molecules at the cell-surface level. This receptor subfamily shares approx. 30% identity among members, with some limited cross-over between ligand activities. Generalized expression patterns within the pancreatic beta-cell, adipose depots and the gastrointestinal tract infer involvement in energy source recognition, absorption, storage and/or metabolism. GPR40, activated by medium and long-chain fatty acids, has been shown to potentiate insulin secretion at the beta-cell, and has been hypothesized to participate in the detrimental effects of chronic fatty acid exposure on beta-cell function. GPR41 and GPR43 have been reported to stimulate leptin release and adipogenesis respectively via activation by short-chain fatty acids. These common themes implicate GPR40, GPR41 and GPR43 in playing significant roles in metabolic diseases, such as diabetes, obesity and the metabolic syndrome.
引用
收藏
页码:770 / 773
页数:4
相关论文
共 36 条
[1]
Molecular or pharmacologic perturbation of the link between glucose and lipid metabolism is without effect on glucose-stimulated insulin secretion - A re-evaluation of the long-chain acyl-CoA hypothesis [J].
Antinozzi, PA ;
Segall, L ;
Prentki, M ;
McGarry, JD ;
Newgard, CB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (26) :16146-16154
[2]
Influence of orally and rectally administered propionate on cholesterol and glucose metabolism in obese rats [J].
Berggren, AM ;
Nyman, EMGL ;
Lundquist, I ;
Bjorck, IME .
BRITISH JOURNAL OF NUTRITION, 1996, 76 (02) :287-294
[3]
Pharmacological regulation of insulin secretion in MIN6 cells through the fatty acid receptor GPR40: identification of agonist and antagonist small molecules [J].
Briscoe, Celia P. ;
Peat, Andrew J. ;
McKeown, Stephen C. ;
Corbett, David F. ;
Goetz, Aaron S. ;
Littleton, Thomas R. ;
McCoy, David C. ;
Kenakin, Terry P. ;
Andrews, John L. ;
Ammala, Carina ;
Fornwald, James A. ;
Ignar, Diane M. ;
Jenkinson, Stephen .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 148 (05) :619-628
[4]
The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acids [J].
Briscoe, CP ;
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 .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (13) :11303-11311
[5]
A family of fatty acid binding receptors [J].
Brown, AJ ;
Jupe, S ;
Briscoe, CP .
DNA AND CELL BIOLOGY, 2005, 24 (01) :54-61
[6]
The orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids [J].
Brown, AJ ;
Goldsworthy, SM ;
Barnes, AA ;
Eilert, MM ;
Tcheang, L ;
Daniels, D ;
Muir, AI ;
Wigglesworth, MJ ;
Kinghorn, I ;
Fraser, NJ ;
Pike, NB ;
Strum, JC ;
Steplewski, KM ;
Murdock, PR ;
Holder, JC ;
Marshall, FH ;
Szekeres, PG ;
Wilson, S ;
Ignar, DM ;
Foord, SM ;
Wise, A ;
Dowell, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (13) :11312-11319
[7]
Circulating fatty acids are essential for efficient glucose-stimulated insulin secretion after prolonged fasting in humans [J].
Dobbins, RL ;
Chester, MM ;
Daniels, MB ;
McGarry, JD ;
Stein, DT .
DIABETES, 1998, 47 (10) :1613-1618
[8]
A fatty acid-dependent step is critically important for both glucose- and non-glucose-stimulated insulin secretion [J].
Dobbins, RL ;
Chester, MW ;
Stevenson, BE ;
Daniels, MB ;
Stein, DT ;
McGarry, JD .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (11) :2370-2376
[9]
THE ROLE OF PROPIONATE AND ACETATE IN THE CONTROL OF FOOD-INTAKE IN SHEEP [J].
FARNINGHAM, DAH ;
WHYTE, CC .
BRITISH JOURNAL OF NUTRITION, 1993, 70 (01) :37-46
[10]
Reduction in voltage-gated K+ currents in primary cultured rat pancreatic β-cells by linoleic acids [J].
Feng, DD ;
Luo, ZQ ;
Roh, SG ;
Hernandez, M ;
Tawadros, N ;
Keating, DJ ;
Chen, C .
ENDOCRINOLOGY, 2006, 147 (02) :674-682