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The role of G-proteins in the dimerisation of human somatostatin receptor types 2 and 5
被引:19
作者:
Grant, Michael
[2
]
Kumar, Ujendra
[1
]
机构:
[1] Univ British Columbia, Fac Pharmaceut Sci, Div Pharmacol & Toxicol, Vancouver, BC V6T 1RZ, Canada
[2] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ, Canada
关键词:
Somatostatin;
Somatostatin receptors;
G-protein-coupled receptors;
Dimerisation;
Heterodimerisation;
Dissociation;
Pertussis toxin;
Fluorescence resonance energy transfer;
COUPLED-RECEPTOR;
PERTUSSIS-TOXIN;
SIGNALING COMPLEXES;
LIGAND-BINDING;
CELL-SURFACE;
LIVE CELLS;
CHO-CELLS;
HETERODIMERIZATION;
INTERNALIZATION;
TRAFFICKING;
D O I:
10.1016/j.regpep.2009.08.011
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Somatostatin (SST) is a peptide hormone that acts through a family of heptahelical receptors belonging to the G-protein coupled receptor (GPCR) superfamily. There are five known SST receptor subtypes termed SSTR1-5 and all couple to G alpha(i/o) G-proteins. It has been previously demonstrated that these receptors can form both homo- and heterodimers within their family or with other GPCR family members. Although agonist was demonstrated as a factor in modulating certain dimeric pairs, the molecular mechanism(s) underlying this regulation remains undetermined. Here, we demonstrate the coupling of C-protein as a contributing factor in the homo- and heterodimerisation of human (h) SSTR2 and SSTR5. When cells stably expressing hSSTR2 are pretreated with pertussis toxin (M), dissociation of hSSTR2 dimers occurs. Interestingly, although dimerisation of hSSTR5 was unaffected following M treatment, heterodimerisation between hSSTR2 and hSSTR5 is potentiated in the absence of receptor-stimulation. These results demonstrate the importance of G-protein in the maintenance and regulation of hSSTR dimers. (C) 2009 Elsevier B.V. All rights reserved.
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页码:3 / 8
页数:6
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