Adenylyl cyclase interaction with the D2 dopamine receptor family; Differential coupling to Gi, Gz, and Gs

被引:76
作者
Obadiah, J
Avidor-Reiss, T
Fishburn, CS
Carmon, S
Bayewitch, M
Vogel, Z
Fuchs, S [1 ]
Levavi-Sivan, B
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Neurobiol, IL-76100 Rehovot, Israel
关键词
GTP-binding protein Gz; GTP-binding protein Gs; GTP-binding protein Gi; D2; (D-2; D-; D-3; D- D-4) dopamine receptor; adenylyl cyclase;
D O I
10.1023/A:1006988603199
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. The D2-type dopamine receptors are thought to inhibit adenylyl cyclase (AC), via coupling to pertussis toxin (PTX)-sensitive G proteins of the Gi family. We examined whether and to what extent the various D2 receptors (D-2S, D-2L, D-3S, D-3L, and D-4) couple to the PTX-insensitive G protein Gz, to produce inhibition of AC activity. 2. COS-7 cells were transiently transfected with the individual murine dopamine receptors alone, as well as together with the Lu subunit of Gz. PTX treatment was employed to inactivate endogenous alpha i, and coupling to Gi and Gz was estimated by measuring the inhibition of cAMP accumulation induced by quinpirole, in forskolin-stimulated cells. 3. D-2S or D-2L receptors can couple to the same extent to Gi and to Gz. The D-4 dopamine receptor couples preferably to Gz, resulting in about 60% quinpirole-induced inhibition of cAMP accumulation. The D-3S, and D-3L receptor isoforms couple slightly to Gz and result in 15 and 30% inhibition of cAMP accumulation, respectively. 4. We have demonstrated for the first time that the two D-3 receptor isoforms, and not any of the other D2 receptor subtypes, also couple to Gs in both COS-7 and CHO transfected cells, in the presence of PTX. 5. Thus, the differential coupling of the D2 dopamine receptor subtypes to various G proteins may add another aspect to the diversity of dopamine receptor function.
引用
收藏
页码:653 / 664
页数:12
相关论文
共 40 条
[1]  
AVIDORREISS T, 1995, J BIOL CHEM, V270, P29732
[2]  
BURFORD NT, 1995, J PHARMACOL EXP THER, V274, P134
[3]   MODULATION OF COCAINE SELF-ADMINISTRATION IN THE RAT THROUGH D-3 DOPAMINE-RECEPTORS [J].
CAINE, SB ;
KOOB, GF .
SCIENCE, 1993, 260 (5115) :1814-1816
[4]  
CASEY PJ, 1990, J BIOL CHEM, V265, P2383
[5]  
CHAN JSC, 1995, J NEUROCHEM, V65, P2682
[6]  
CHIO CL, 1994, J BIOL CHEM, V269, P11813
[7]  
CHIO CL, 1994, MOL PHARMACOL, V45, P51
[8]   REGULATION AND FUNCTIONAL-CHARACTERIZATION OF A RAT RECOMBINANT DOPAMINE D3 RECEPTOR [J].
COX, BA ;
ROSSER, MP ;
KOZLOWSKI, MR ;
DUWE, KM ;
NEVE, RL ;
NEVE, KA .
SYNAPSE, 1995, 21 (01) :1-9
[9]  
DAVID C, 1991, MOL PHARMACOL, V40, P712
[10]   D2 DOPAMINE-RECEPTORS IN THE HUMAN RETINA - CLONING OF CDNA AND LOCALIZATION OF MESSENGER-RNA [J].
DEARRY, A ;
FALARDEAU, P ;
SHORES, C ;
CARON, MG .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 1991, 11 (05) :437-453