Obestatin does not activate orphan G protein-coupled receptor GPR39

被引:207
|
作者
Lauwers, Erwin
Landuyt, Bart
Arckens, Lutgarde
Schoofs, Liliane
Luyten, Walter
机构
[1] Katholieke Univ Leuven, Lab Dev Physiol Genom & Proteom, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Sch Med, Dept Gynaecol, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Lab Neuroplasticity & Neuroproteom, B-3000 Louvain, Belgium
关键词
obestatin; GPR39; GPCR;
D O I
10.1016/j.bbrc.2006.09.141
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
Recently, the ligand of the orphan G protein-coupled receptor GPR39 has been identified as obestatin, a 23-amino acid peptide derived from the ghrelin precursor protein. We used two methods to study the possible activation of GPR39 by obestatin: cAMP measurements based on a luminescent reporter gene and a fluorometric Ca2+ flux method. The former was similar to that reported in the original publication of Zhang et al. [J.V. Zhang, P.G. Ren, O. Avsian-Kretchmer, C.W. Luo, R. Rauch, C. Klein, Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake, Science 310 (2005) 996-999]. The latter method used promiscuous as well as chimaeric G-proteins commonly used to couple orphan G protein-coupled receptors to the phospholipase C pathway, that leads to intracellular Ca2+ rise. We could, however, not demonstrate activation of the GPR39 receptor by obestatin via any of these signal transduction pathways. We could activate GPR39 by high concentrations of Zn2+, demonstrating cell surface expression of a functional receptor that could elicit a Ca2+ response. The Zn2+ response was not affected by obestatin. The identity of the native ligand for GPR39 remains to be elucidated. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 25
页数:5
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