Loading…

Molecular Cloning, Functional Expression, Pharmacological Characterization and Chromosomal Localization of the Human Metabotropic Glutamate Receptor Type 3

Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on the...

Full description

Saved in:
Bibliographic Details
Published in:Neuropharmacology 1996-05, Vol.35 (5), p.523-530
Main Authors: EMILE, LYDIA, MERCKEN, LUC, APIOU, FRANCOISE, PRADIER, LAURENT, BOCK, MARIE-DOMINIQUE, MENAGER, JEAN, CLOT, JOSETTE, DOBLE, ADAM, BLANCHARD, JEAN-CHARLES
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Glutamic acid is the major excitatory amino acid of the central nervous system which interacts with two receptor families, the ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) are coupled to G proteins and can be divided into three subgroups based on their sequence homology, signal transduction pathway and pharmacology. In this study, we describe the cloning of the cDNA encoding the human metabotropic glutamate receptor type 3 (HmGluR3). It was obtained by reverse transcription-polymerase chain reaction (RT-PCR) with degenerate oligonucleotides corresponding to highly conserved sequences between rat mGluRs. The receptor shows 879 amino acids with 96% amino acid sequence identity with rat mGluR3. It is strongly expressed in fetal and adult whole brain, especially in caudate nucleus and corpus callosum. The gene was identified by fluorescence in situ hybridization on chromosome 7 band q22. Activation of the human mGluR3, permanently expressed in Baby Hamster Kidney (BHK) cells, by excitatory amino acid inhibits the forskolin-stimulated accumulation of intracellular cAMP. The rank order of potency is l-glutamic acid ⩾ (1 S,3 R)-1-aminocyclopentane-1,3-dicarboxylic acid ((1 S,3 R)-ACPD) >> ibotenic acid > quisqualic acid. ( RS)-α-methyl-4-carboxyphenylglycine [( RS)-MCPG, 1 mM] is without effect on inhibition of forskolin-induced cAMP accumulation by l-glutamic acid. Copyright © 1996 Elsevier Science Ltd.
ISSN:0028-3908
1873-7064
DOI:10.1016/0028-3908(96)84622-3