The M3 muscarinic acetylcholine receptor expressed in HEK-293 cells signals to phospholipase D via G12 but not Gq-type G proteins -: Regulators of G proteins as tools to dissect pertussis toxin-resistant G proteins in receptor-effector coupling

被引:73
作者
Rümenapp, U
Asmus, M
Schablowski, H
Woznicki, M
Han, L
Jakobs, KH
Fahimi-Vahid, M
Michalek, C
Wieland, T
Schmidt, M
机构
[1] Univ Essen Gesamthsch Klinikum, Inst Pharmakol, D-45122 Essen, Germany
[2] Univ Hamburg, Krankenhaus Eppendorf, Inst Expt & Klin Pharmakol & Toxicol, D-20246 Hamburg, Germany
关键词
D O I
10.1074/jbc.M004957200
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
The M-3 muscarinic acetylcholine receptor (mAChR) expressed in HEK-293 cells couples to G(q) and G(12) proteins and stimulates phospholipase C (PLC) and phospholipase D (PLD) in a pertussis toxin-insensitive manner. To determine the type of G protein mediating M-3 mAChR-PLD coupling in comparison to M-3 mAChR-PLC coupling, we expressed various G alpha proteins and regulators of the G protein signaling (RGS), which act as GTPase-activating proteins for G(q)- or G(12)-type G proteins. PLD stimulation by the M-3 mAChR was enhanced by the overexpression of G alpha (12), and G alpha (13), whereas the overexpression of G alpha (q) strongly increased PLC activity without affecting PLD activity. Expression of the RGS homology domain of Lsc, which acts specifically on G alpha (12) and G alpha (13), blunted the M-3 mAChR-induced PLD stimulation without affecting PLC stimulation. On the other hand, overexpression of RGS4, which acts on G alpha (q)- but not G alpha (12)-type G proteins, suppressed the M-3 mAChR-induced PLC stimulation without altering PLD stimulation. We conclude that the M-3 mAChR in HEK-293 cells apparently signals to PLD via G alpha (q)- but not G alpha (12)-type G proteins and that G protein subtype-selective RGS proteins can be used as powerful tools to dissect the pertussis toxin-resistant G proteins and their role in receptor-effector coupling.
引用
收藏
页码:2474 / 2479
页数:6
相关论文
共 45 条
[1]   Mammalian RGS proteins: Barbarians at the gate [J].
Berman, DM ;
Gilman, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) :1269-1272
[2]   The GTPase-activating protein RGS4 stabilizes the transition state for nucleotide hydrolysis [J].
Berman, DM ;
Kozasa, T ;
Gilman, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) :27209-27212
[3]   G-ALPHA(12) AND G-ALPHA(13) STIMULATE RHO-DEPENDENT STRESS FIBER FORMATION AND FOCAL ADHESION ASSEMBLY [J].
BUHL, AM ;
JOHNSON, NL ;
DHANASEKARAN, N ;
JOHNSON, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :24631-24634
[4]   RGS proteins: more than just GAPs for heterotrimeric G proteins [J].
De Vries, L ;
Farquhar, MG .
TRENDS IN CELL BIOLOGY, 1999, 9 (04) :138-144
[5]   Signaling by the G(12) class of G proteins [J].
Dhanasekaran, N ;
Dermott, JM .
CELLULAR SIGNALLING, 1996, 8 (04) :235-245
[6]   Phospholipase D: Enzymology, mechanisms of regulation, and function [J].
Exton, JH .
PHYSIOLOGICAL REVIEWS, 1997, 77 (02) :303-320
[7]   Regulation of phospholipase D [J].
Exton, JH .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 1999, 1439 (02) :121-133
[8]   ADP-ribosylation factor and Rho proteins mediate fMLP-dependent activation of phospholipase D in human neutrophils [J].
Fensome, A ;
Whatmore, J ;
Morgan, C ;
Jones, D ;
Cockcroft, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13157-13164
[9]   The small GTP-binding protein Rho links G protein-coupled receptors and G alpha(12) to the serum response element and to cellular transformation [J].
Fromm, C ;
Coso, OA ;
Montaner, S ;
Xu, NZ ;
Gutkind, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10098-10103
[10]   Apparent up-regulation of stimulatory G-protein α subunits in the pregnant human myometrium is mimicked by elevated smoothelin expression [J].
Gsell, S ;
Eschenhagen, T ;
Kaspareit, G ;
Nose, M ;
Scholz, H ;
Behrens, O ;
Wieland, T .
FASEB JOURNAL, 2000, 14 (01) :17-26