Dopamine D2 receptors in signal transduction and behavior

被引:103
作者
Picetti, R
Saiardi, A
Samad, TA
Bozzi, Y
Baik, JH
Borrelli, E
机构
[1] ULP, CNRS, INSERM, INST GENET & BIOL MOL & CELLULAIRE, F-67404 ILLKIRCH GRAFFENSTADEN, FRANCE
[2] YONSEI UNIV, COLL MED, MOL BIOL LAB, MED RES CTR, SEOUL, SOUTH KOREA
[3] CU STRASBOURG, STRASBOURG, FRANCE
来源
CRITICAL REVIEWS IN NEUROBIOLOGY | 1997年 / 11卷 / 2-3期
关键词
seven transmembrane domain G-protein-coupled receptors; basal ganglia; pharmacology; signal transduction; knockout; Parkinson's disease;
D O I
10.1615/CritRevNeurobiol.v11.i2-3.20
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The dopamine D2 receptor belongs to the family of seven transmembrane domain G-protein-coupled receptors and is highly expressed in the central nervous system and the pituitary gland. The binding of dopamine to the D2 receptor is crucial for the regulation of diverse physiological functions, such as the control of locomotor activity and the synthesis of peptide hormones. Two alternatively spliced transcripts are generated from the D2 receptor gene and code for the D2L and D2S isoforms, which are 444 and 415 amino acids in length, respectively. These isoforms exhibit similar pharmacological characteristics and are expressed in the same cell types, with a ratio that normally favors expression of the longer isoform. The D2L isoform differs from D2S by the insertion of 29 amino acids in the putative third intracellular loop of the receptor. This loop is involved in the coupling of the receptor to different G proteins. Experiments have shown that the D2 isoforms have different G-protein-coupling affinities, suggesting that these receptors might serve different functions in vivo. Additionally, this difference in coupling affinity could be a mechanism to amplify the signal transduced by the binding of dopamine to D2 receptors. Important insights into D2 receptor function in vivo have been obtained by knocking out the D2 gene in mice. The Parkinsonian-like phenotype of D2-null mice demonstrates the importance of the D2 receptor for locomotor function.
引用
收藏
页码:121 / 142
页数:22
相关论文
共 129 条
[61]  
KOCH BD, 1988, J BIOL CHEM, V263, P216
[62]  
KOZELL LB, 1994, J BIOL CHEM, V269, P30299
[63]   LOCATION OF A REGION OF THE MUSCARINIC ACETYLCHOLINE-RECEPTOR INVOLVED IN SELECTIVE EFFECTOR COUPLING [J].
KUBO, T ;
BUJO, H ;
AKIBA, I ;
NAKAI, J ;
MISHINA, M ;
NUMA, S .
FEBS LETTERS, 1988, 241 (1-2) :119-125
[64]   DIFFERENT EXPRESSION OF THE 2 DOPAMINERGIC D2 RECEPTORS, D2415 AND D2444, IN 2 TYPES OF LACTOTROPH EACH CHARACTERIZED BY THEIR RESPONSE TO DOPAMINE, AND MODIFICATION OF EXPRESSION BY SEX STEROIDS [J].
KUKSTAS, LA ;
DOMEC, C ;
BASCLES, L ;
BONNET, J ;
VERRIER, D ;
ISRAEL, JM ;
VINCENT, JD .
ENDOCRINOLOGY, 1991, 129 (02) :1101-1103
[65]   PHENOTYPICAL CHARACTERIZATION OF THE RAT STRIATAL NEURONS EXPRESSING THE D1 DOPAMINE RECEPTOR GENE [J].
LEMOINE, C ;
NORMAND, E ;
BLOCH, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (10) :4205-4209
[66]   IDENTIFICATION, CHARACTERIZATION, AND LOCALIZATION OF THE DOPAMINE-D3 RECEPTOR IN RAT-BRAIN USING 7-[H-3]HYDROXY-N,N-DI-NORMAL-PROPYL-2-AMINOTETRALIN [J].
LEVESQUE, D ;
DIAZ, J ;
PILON, C ;
MARTRES, MP ;
GIROS, B ;
SOUIL, E ;
SCHOTT, D ;
MORGAT, JL ;
SCHWARTZ, JC ;
SOKOLOFF, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8155-8159
[67]   DOPAMINE NEURON MEMBRANE PHYSIOLOGY - CHARACTERIZATION OF THE TRANSIENT OUTWARD CURRENT (I-A) AND DEMONSTRATION OF A COMMON SIGNAL-TRANSDUCTION PATHWAY FOR I-A AND I-K [J].
LIU, LX ;
SHEN, RY ;
KAPATOS, G ;
CHIODO, LA .
SYNAPSE, 1994, 17 (04) :230-240
[68]  
LIU YF, 1994, J BIOL CHEM, V269, P13880
[69]   DIFFERENTIAL G-PROTEIN MEDIATED COUPLING OF D2 DOPAMINE-RECEPTORS TO K+ AND CA2+ CURRENTS IN RAT ANTERIOR-PITUITARY-CELLS [J].
LLEDO, PM ;
HOMBURGER, V ;
BOCKAERT, J ;
VINCENT, JD .
NEURON, 1992, 8 (03) :455-463
[70]  
MALGAROLI A, 1987, J BIOL CHEM, V262, P13920