Coupling of dopamine receptor subtypes to multiple and diverse G proteins

被引:93
作者
Sidhu, A
Niznik, HB
机构
[1] Georgetown Univ, Med Ctr, Dept Pediat, Lab Mol Neurochem, Washington, DC 20007 USA
[2] Univ Toronto, Dept Pharmacol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[4] Ctr Addict & Mental Hlth, Mol Neurobiol Lab, Toronto, ON M5T 1R8, Canada
基金
美国国家卫生研究院;
关键词
dopamine receptors; G proteins; signal transduction; schizophrenia; Parkinsons disease; attention deficit hyperactivity disorder;
D O I
10.1016/S0736-5748(00)00033-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The family of five dopamine receptors subtypes activate cellular effector systems through G proteins. Historically, dopamine receptors were thought to only stimulate or inhibit adenylyl cyclase, by coupling to either G(s)alpha or G(i)alpha, respectively. Recent studies in transfected cells, reviewed hers, have shown that multiple and highly diverse signaling pathways are activated by specific dopamine receptor subtypes. This multiplicity of signaling responses occurs through selective coupling to distinct G proteins and each of the receptors can interact with more than one G protein. Although some of the multiple coupling of dopamine receptors to different G proteins occurs from within the same family of G proteins, these receptors can also couple to G proteins belonging to different families. Such multiple interactions between receptors and G proteins elicits functionally distinct physiological effects which acts to enhance and subsequently suppress the original receptor response, and to activate apparently distinct signaling pathways. In the brain, where coexpression of functionally distinct receptors in heterogenous cells further adds to the complexity of dopamine signaling, minor alterations in receptor/G protein coupling states during either development or in adults, may underlie the imbalanced signaling seen in dopaminergic-linked diseases such as schizophrenia, Parkinson's disease and attention deficit hyperactivity disorder. reserved.
引用
收藏
页码:669 / 677
页数:9
相关论文
共 88 条
[1]   In vivo regulation of central nervous system progesterone receptors: Cocaine induces steroid-dependent behavior through dopamine transporter modulation of D5 receptors in rats [J].
Apostolakis, EM ;
Garai, J ;
Clark, JH ;
OMalley, BW .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (12) :1595-1604
[2]   Striatal excitatory amino acid receptor subunit expression in the D1A-dopamine receptor-deficient mouse [J].
Ariano, MA ;
Drago, J ;
Sibley, DR ;
Levine, MS .
DEVELOPMENTAL NEUROSCIENCE, 1998, 20 (2-3) :237-241
[3]   Can functional regions of proteins be predicted from their coding sequences? The case study of G-protein coupled receptors (Reprinted from Gene, vol 221, pg GC65-GC110, 1998) [J].
Arrigo, P ;
Fariselli, P ;
Casadio, R .
GENE, 1998, 221 (01) :GC65-GC110
[4]  
Baldessarini R. J., 1997, DOPAMINE RECEPTORS, P457, DOI [10.1007/978-1-4757-2635-0_15, DOI 10.1007/978-1-4757-2635-0_15]
[5]   Neuropharmacological mechanisms of drug reward: Beyond dopamine in the nucleus accumbens [J].
Bardo, MT .
CRITICAL REVIEWS IN NEUROBIOLOGY, 1998, 12 (1-2) :37-67
[6]   Dopamine D1-like receptors and reward-related incentive learning [J].
Beninger, RJ ;
Miller, R .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1998, 22 (02) :335-345
[7]   INHIBITION BY DOPAMINE OF (NA++K+)ATPASE ACTIVITY IN NEOSTRIATAL NEURONS THROUGH D1 AND D2 DOPAMINE RECEPTOR SYNERGISM [J].
BERTORELLO, AM ;
HOPFIELD, JF ;
APERIA, A ;
GREENGARD, P .
NATURE, 1990, 347 (6291) :386-388
[8]   G protein-mediated mitogen-activated protein kinase activation by two dopamine D2 receptors [J].
Choi, EY ;
Jeong, DW ;
Park, KW ;
Baik, JH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 256 (01) :33-40
[9]   Effects of repeated amphetamine treatment on the locomotor activity of the dopamine D-1A-deficient mouse [J].
Crawford, CA ;
Drago, J ;
Watson, JB ;
Levine, MS .
NEUROREPORT, 1997, 8 (11) :2523-2527
[10]   Switching of the coupling of the beta(2)-adrenergic receptor to different G proteins by protein kinase A [J].
Daaka, Y ;
Luttrell, LM ;
Lefkowitz, RJ .
NATURE, 1997, 390 (6655) :88-91