Ectopically expressed gamma-aminobutyric acid receptor B is functionally down-regulated in isolated lipid raft-enriched membranes
Title | Ectopically expressed gamma-aminobutyric acid receptor B is functionally down-regulated in isolated lipid raft-enriched membranes |
Publication Type | Journal Article |
Year of Publication | 2004 |
Authors | Becher, A, Green A, Ige AO, Wise A, White JH, McIlhinney RA |
Journal | Biochem Biophys Res Commun |
Volume | 321 |
Pagination | 981-7 |
Date Published | Sep 3 |
ISBN Number | 0006-291X (Print)0006-291X (Linking) |
Accession Number | 15358124 |
Keywords | Animals, Cerebellum/metabolism, CHO Cells, Cricetinae, Down-Regulation, Gene Expression, Guanosine 5'-O-(3-Thiotriphosphate)/metabolism, Immunohistochemistry, Membrane Microdomains/metabolism, Rats, Receptors, GABA-B/agonists/*genetics/*metabolism, Recombinant Proteins/genetics/metabolism |
Abstract | Lipid raft domains have attracted much recent attention as platforms for plasma membrane signalling complexes. In particular, evidence is emerging that shows them to be key regulators of G protein coupled receptor function. The G protein coupled gamma-aminobutyric acid receptor B (GABA(B) receptor) co-isolates with lipid raft domains from rat brain cerebellum. In the present study, we show that the GABA(B1a,2) receptor was also present in lipid raft domains when expressed ectopically in a Chinese hamster ovary cell line. Lipid raft-associated receptor was functionally active, displaying a concentration-dependent increase in GTPgammaS binding in response to the receptor agonist GABA. Compared with whole cell membranes, lipid raft-associated receptor displayed an increased EC(50) and a reduced magnitude of response to GABA. We conclude that lipid raft association is an intrinsic property of the GABA(B1a,2) receptor and is not cell-type specific. In addition, localisation to lipid raft domains may provide a mechanism to inhibit receptor function. |
URL | http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15358124 |