G protein-coupled receptors: walking hand-in-hand, talking hand-in-hand?

被引:29
作者
Vischer, Henry F. [1 ]
Watts, Anne O. [1 ]
Nijmeijer, Saskia [1 ]
Leurs, Rob [1 ]
机构
[1] Vrije Univ Amsterdam, LACDR, Div Med Chem, Fac Sci, NL-1081 HV Amsterdam, Netherlands
关键词
G protein-coupled receptor; receptor dimerization; receptor oligomerization; receptor trafficking; cooperativity; crosstalk; G protein; signal transduction; TERMINAL EXTRACELLULAR DOMAIN; FOLLICLE-STIMULATING-HORMONE; V2 VASOPRESSIN RECEPTORS; HIGHER-ORDER OLIGOMERS; TIME-RESOLVED FRET; CROSS-TALK; GABA(B) RECEPTOR; ENERGY-TRANSFER; CB1; RECEPTOR; PHARMACOLOGICAL CHAPERONES;
D O I
10.1111/j.1476-5381.2011.01229.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Most cells express a panel of different G protein-coupled receptors (GPCRs) allowing them to respond to at least a corresponding variety of extracellular ligands. In order to come to an integrative well-balanced functional response these ligand-receptor pairs can often cross-regulate each other. Although most GPCRs are fully capable to induce intracellular signalling upon agonist binding on their own, many GPCRs, if not all, appear to exist and function in homomeric and/or heteromeric assemblies for at least some time. Such heteromeric organization offers unique allosteric control of receptor pharmacology and function between the protomers and might even unmask 'new' features. However, it is important to realize that some functional consequences that are proposed to originate from heteromeric receptor interactions may also be observed due to intracellular crosstalk between signalling pathways of non-associated GPCRs.
引用
收藏
页码:246 / 260
页数:15
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