A role for membrane potential in regulating GPCRs?

被引:81
作者
Mahaut-Smith, Martyn P. [1 ]
Martinez-Pinna, Juan [2 ]
Gurung, Iman S. [3 ]
机构
[1] Univ Leicester, Dept Cell Physiol & Pharmacol, Leicester LE1 9HN, Leics, England
[2] Univ Alicante, Div Fisiol, E-03080 Alicante, Spain
[3] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EG, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.tips.2008.05.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G-protein-coupled receptors (GPCRs) have ubiquitous roles in transducing extracellular signals into cellular responses. Therefore, the concept that members of this superfamily of surface proteins are directly modulated by changes in membrane voltage could have widespread consequences for cell signalling. Although several studies have indicated that GPCRs can be voltage dependent, particularly P2Y(1) receptors in the non-excitable megakaryocyte, the evidence has been mostly indirect. Recent work on muscarinic receptors has stimulated substantial interest in this field by reporting the first voltage-dependent charge movements for a GPCR. An underlying mechanism is proposed whereby a voltage-induced conformational change in the receptor alters its ability to couple to the G protein and thereby influences its affinity for an agonist. We discuss the strength of the evidence behind this hypothesis and include suggestions for future work. We also describe other examples in which direct voltage control of GPCRs can account for effects of membrane potential on downstream signals and highlight the possible physiological consequences of this phenomenon.
引用
收藏
页码:421 / 429
页数:9
相关论文
共 71 条
[61]  
SULLIVAN JM, 2001, BIOPHYS J
[62]   Oscillations of phospholipase C activity triggered by depolarization and Ca2+ influx in insulin-secreting cells [J].
Thore, S ;
Dyachok, O ;
Tengholm, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (19) :19396-19400
[63]  
TRISSL HW, 1982, BIOPHYS STRUCT MECH, V8, P213, DOI 10.1007/BF00535460
[64]   Metabotropic Ca2+ channel-induced calcium release in vascular smooth muscle [J].
Urena, Juan ;
Del Valle-Rodriguez, Alberto ;
Lopez-Barneo, Jose .
CELL CALCIUM, 2007, 42 (4-5) :513-520
[65]  
VALLERODRIGUEZ A, 2006, P NATL ACAD SCI USA, V103, P4316
[66]  
VALLERODRIGUEZ A, 2003, EMBO J, V22, P4337
[67]   INOSITOL 1,4,5-TRISPHOSPHATE - A POSSIBLE CHEMICAL LINK IN EXCITATION-CONTRACTION COUPLING IN MUSCLE [J].
VERGARA, J ;
TSIEN, RY ;
DELAY, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (18) :6352-6356
[68]   A study of P2X1 receptor function in murine megakaryocytes and human platelets reveals synergy with P2Y receptors [J].
Vial, C ;
Rolf, MG ;
Mahaut-Smith, MP ;
Evans, RJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 135 (02) :363-372
[69]   RYANODINE AND INOSITOL TRISPHOSPHATE RECEPTORS COEXIST IN AVIAN CEREBELLAR PURKINJE NEURONS [J].
WALTON, PD ;
AIREY, JA ;
SUTKO, JL ;
BECK, CF ;
MIGNERY, GA ;
SUDHOF, TC ;
DEERINCK, TJ ;
ELLISMAN, MH .
JOURNAL OF CELL BIOLOGY, 1991, 113 (05) :1145-1157
[70]   Voltage-induced membrane movement [J].
Zhang, PC ;
Keleshian, AM ;
Sachs, F .
NATURE, 2001, 413 (6854) :428-432