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
[1]   Origin of functional diversity among tetrameric voltage-gated channels [J].
Anselmi, Claudio ;
Carloni, Paolo ;
Torre, Vincent .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2007, 66 (01) :136-146
[2]   Dihydropyridine receptors as voltage sensors for a depolarization-evoked, IP3R-mediated, slow calcium signal in skeletal muscle cells [J].
Araya, R ;
Liberona, JL ;
Cárdenas, JC ;
Riveros, N ;
Estrada, M ;
Powell, JA ;
Carrasco, MA ;
Jaimovich, E .
JOURNAL OF GENERAL PHYSIOLOGY, 2003, 121 (01) :3-16
[3]  
ARNIS S, 1994, J BIOL CHEM, V269, P23879
[4]   The M2 muscarinic G-protein-coupled receptor is voltage-sensitive [J].
Ben-Chaim, Y ;
Tour, O ;
Dascal, N ;
Parnas, I ;
Parnas, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (25) :22482-22491
[5]   Movement of 'gating charge' is coupled to ligand binding in a G-protein-coupled receptor [J].
Ben-Chaim, Yair ;
Chanda, Baron ;
Dascal, Nathan ;
Bezanilla, Francisco ;
Parnas, Itzchak ;
Parnas, Hanna .
NATURE, 2006, 444 (7115) :106-109
[6]   DEPOLARIZATION OF GUINEA-PIG VISCERAL SMOOTH-MUSCLE CAUSES HYDROLYSIS OF INOSITOL PHOSPHOLIPIDS [J].
BEST, L ;
BOLTON, TB .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1986, 333 (01) :78-82
[7]   The voltage sensor in voltage-dependent ion channels [J].
Bezanilla, F .
PHYSIOLOGICAL REVIEWS, 2000, 80 (02) :555-592
[8]   Modulation of Gq-protein-coupled inositol trisphosphate and Ca2+ signaling by the membrane potential [J].
Billups, Daniela ;
Billups, Brian ;
Challiss, R. A. John ;
Nahorski, Stefan R. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (39) :9983-9995
[9]  
BOLTON TB, 2003, SCI STKE, pE52
[10]   NEW RECEPTOR POTENTIAL OF MONKEY RETINA WITH NO DETECTABLE LATENCY [J].
BROWN, KT ;
MURAKAMI, M .
NATURE, 1964, 201 (491) :626-&