GPR40 is expressed in glucagon producing cells and affects glucagon secretion

被引:93
作者
Flodgren, Erik [1 ]
Olde, Bjorn
Meidute-Abaraviciene, Sandra
Winzell, Maria Sorhede
Ahren, Bo
Salehi, Albert
机构
[1] Lund Univ, Ctr Biomed, Dept Clin Sci, Lund, Sweden
[2] Lund Univ, Ctr Biomed, Dept Expt Med Sci, Lund, Sweden
[3] Malmo Univ Hosp, Clin Res Ctr, Dept Clin Sci, Malmo, Sweden
关键词
GPR40; free fatty acid; alpha-cell; glucagon; pancreatic islets; diabetes;
D O I
10.1016/j.bbrc.2006.12.193
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
The free fatty acid receptor, GPR40, has been coupled with insulin secretion via its expression in pancreatic beta-cells. However, the role of GPR40 in the release of glucagon has not been studied and previous attempts to identify the receptor in alpha-cells have been unfruitful. Using double-staining for glucagon and GPR40 expression, we demonstrate that the two are expressed in the same cells in the periphery of mouse islets. In-R1-G9 hamster glucagonoma cells respond dose-dependently to linoleic acid stimulation by elevated phosphatidyl inositol hydrolysis and glucagon release and the cells become increasingly responsive to fatty acid stimulation when overexpressing GPR40. Isolated mouse islets also secrete glucagon in response to linoleic acid, a response that was abolished by antisense treatment against GPR40. This study demonstrates that GPR40 is present and active in pancreatic alpha-cells and puts further emphasis on the importance of this nutrient sensing receptor in islet function. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:240 / 245
页数:6
相关论文
共 20 条
[1]   Stimulatory short-term effects of free fatty acids on glucagon secretion at low to normal glucose concentrations [J].
Bollheimer, LC ;
Landauer, HC ;
Troll, S ;
Schweimer, J ;
Wrede, CE ;
Schölmerich, J ;
Buettner, R .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2004, 53 (11) :1443-1448
[2]   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
[3]   EFFECT OF OLEIC-ACID ON ARGININE-INDUCED GLUCAGON-SECRETION BY THE ISOLATED PERFUSED RAT PANCREAS [J].
CAMPILLO, JE ;
LUYCKX, AS ;
LEFEBVRE, PJ .
ACTA DIABETOLOGICA LATINA, 1979, 16 (04) :287-293
[4]  
DELEAN A, 1980, J BIOL CHEM, V255, P7108
[5]   Intracellular trafficking of hormone receptors [J].
Gáborik, Z ;
Hunyady, L .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2004, 15 (06) :286-293
[6]   The short-term effect of fatty acids on glucagon secretion is influenced by their chain length, spatial configuration, and degree of unsaturation: studies in vitro [J].
Hong, J ;
Abudula, R ;
Chen, JG ;
Jeppesen, PB ;
Dyrskog, SEU ;
Xiao, JZ ;
Colombo, M ;
Hermansen, K .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2005, 54 (10) :1329-1336
[7]   Free fatty acids regulate insulin secretion from pancreatic β cells through GPR40 [J].
Itoh, Y ;
Kawamata, Y ;
Harada, M ;
Kobayashi, M ;
Fujii, R ;
Fukusumi, S ;
Ogi, K ;
Hosoya, M ;
Tanaka, Y ;
Uejima, H ;
Tanaka, H ;
Maruyama, M ;
Satoh, R ;
Okubo, S ;
Kizawa, H ;
Komatsu, H ;
Matsumura, F ;
Noguchi, Y ;
Shinobara, T ;
Hinuma, S ;
Fujisawa, Y ;
Fujino, M .
NATURE, 2003, 422 (6928) :173-176
[8]   Negative and positive regulatory epitopes in the C-terminal domains of the human B1 and B2 bradykinin receptor subtypes determine receptor coupling efficacy to G9/11-mediated phospholipase Cβ activity [J].
Kang, DS ;
Leeb-Lundberg, LMF .
MOLECULAR PHARMACOLOGY, 2002, 62 (02) :281-288
[9]   A human cell surface receptor activated by free fatty acids and thiazolidinedione drugs [J].
Kotarsky, K ;
Nilsson, NE ;
Flodgren, E ;
Owman, C ;
Olde, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (02) :406-410
[10]   PANCREATIC POLYPEPTIDE - POSTULATED NEW HORMONE - IDENTIFICATION OF ITS CELLULAR STORAGE SITE BY LIGHT AND ELECTRON-MICROSCOPIC IMMUNOCYTOCHEMISTRY [J].
LARSSON, LI ;
SUNDLER, F ;
HAKANSON, R .
DIABETOLOGIA, 1976, 12 (03) :211-226