The M2 muscarinic G-protein-coupled receptor is voltage-sensitive

被引:109
作者
Ben-Chaim, Y
Tour, O
Dascal, N
Parnas, I
Parnas, H [1 ]
机构
[1] Hebrew Univ Jerusalem, Otto Loewi Minerva Ctr Cellular & Mol Neurobiol, IL-91904 Jerusalem, Israel
[2] Tel Aviv Univ, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
关键词
D O I
10.1074/jbc.M301146200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G- protein coupled receptors are not considered to exhibit voltage sensitivity. Here, using Xenopus oocytes, we show that the M-2 muscarinic receptor ( m2R) is voltage-sensitive. The m2R- mediated potassium channel ( GIRK) currents were used to assay the activity of m2R. We found that the apparent affinity of m2R toward acetylcholine ( ACh) was reduced upon depolarization. Binding experiments of [ H-3] ACh to individual oocytes expressing m2R confirmed the electrophysiological findings. When the GIRK channels were activated either by overexpression of Gbetagamma subunits or by injection of GTPgammaS, the ratio between the currents measured at -60 mV and + 40 mV was the same as for the basal activity of the GIRK channel. Thus, the steps downstream to agonist activation of m2R are not voltage- sensitive. We further found that, in contrast to m2R, the apparent affinity of m1R was increased upon depolarization. We also found that the voltage sensitivity of binding of [H-3] ACh to oocytes expressing m2R was greatly diminished following pretreatment with pertussis toxin. The cumulative results suggest that m2R is, by itself, voltage- sensitive. Furthermore, the voltage sensitivity does not reside in the ACh binding site, rather, it most likely resides in the receptor region that couples to the G- protein.
引用
收藏
页码:22482 / 22491
页数:10
相关论文
共 39 条
[1]  
BAUD C, 1983, J PHYSL, V356, P275
[2]   2 CALCIUM-ACTIVATED CHLORIDE CONDUCTANCES IN XENOPUS-LAEVIS OOCYTES PERMEABILIZED WITH THE IONOPHORE A23187 [J].
BOTON, R ;
DASCAL, N ;
GILLO, B ;
LASS, Y .
JOURNAL OF PHYSIOLOGY-LONDON, 1989, 408 :511-534
[3]  
Bunemann M, 1996, J PHYSIOL-LONDON, V494, P351
[4]   G-PROTEIN MEDIATES VOLTAGE REGULATION OF AGONIST BINDING TO MUSCARINIC RECEPTORS - EFFECTS ON RECEPTOR-NA+ CHANNEL INTERACTION [J].
COHEN-ARMON, M ;
GARTY, H ;
SOKOLOVSKY, M .
BIOCHEMISTRY, 1988, 27 (01) :368-374
[5]  
COHEN-ARMON M, 1991, J BIOL CHEM, V266, P2595
[6]   Signalling via the G protein-activated K+ channels [J].
Dascal, N .
CELLULAR SIGNALLING, 1997, 9 (08) :551-573
[7]   XENOPUS OOCYTE RESTING POTENTIAL, MUSCARINIC RESPONSES AND THE ROLE OF CALCIUM AND GUANOSINE 3',5'-CYCLIC-MONOPHOSPHATE [J].
DASCAL, N ;
LANDAU, EM ;
LASS, Y .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 352 (JUL) :551-574
[8]  
Dascal N., 1992, METHOD MOL BIOL, V13, P205
[9]   PRESYNAPTIC MUSCARINIC RECEPTORS AND THE RELEASE OF ACETYLCHOLINE FROM CEREBROCORTICAL PRISMS - ROLES OF CA2+ AND K+ CONCENTRATIONS [J].
DOLEZAL, V ;
TUCEK, S .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1993, 348 (03) :228-233
[10]   INTRINSIC GATING PROPERTIES OF A CLONED G-PROTEIN-ACTIVATED INWARD RECTIFIER K+ CHANNEL [J].
DOUPNIK, CA ;
LIM, NF ;
KOFUJI, P ;
DAVIDSON, N ;
LESTER, HA .
JOURNAL OF GENERAL PHYSIOLOGY, 1995, 106 (01) :1-23