Neuronal 5-HT metabotropic receptors:: fine-tuning of their structure, signaling, and roles in synaptic modulation

被引:182
作者
Bockaert, Joel [1 ]
Claeysen, Sylvie
Becamel, Carine
Dumuis, Aline
Marin, Philippe
机构
[1] CNRS, UMR 5203, F-34094 Montpellier, France
[2] INSERM, U661, F-34094 Montpellier, France
[3] Univ Montpellier I, F-34094 Montpellier, France
[4] Univ Montpellier 2, F-34094 Montpellier, France
[5] Inst Genom Fonct, Dept Neurobiol, F-34094 Montpellier 5, France
关键词
serotonin; serotonin receptors; G-protein-coupled receptors; receptosome; signaling;
D O I
10.1007/s00441-006-0286-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Serotonin (5-hydroxytryptamine, 5-HT) is, without doubt, the neurotransmitter for which the number of receptors is the highest. Fifteen genes encoding functional 5-HT receptors have been cloned in mammalian brain. 5-HT3 receptors are ionotropic receptors, whereas all the others are metabotropic G-protein-coupled receptors (GPCRs). 5-HT receptor diversity is further increased by post-genomic modifications, such as alternative splicing (up to 10 splice variants for the 5-HT4 receptor) or by mRNA editing in the case of 5-HT2C receptors. The cellular and behavioral implications of 5-HT2C receptor editing are of great physiological importance. Signaling of 5-HT receptors involves a great variety of pathways, but only some of these have been demonstrated in neurons. The classical view of neurotransmitter receptors localized within the synaptic cleft cannot be applied to 5-HT receptors, which are mostly (but not exclusively) localized at extra-synaptic locations either pre- or post-synaptically. 5-HT receptors are engaged in pre- or post-synaptic complexes composed of many GPCR-interacting proteins. The functions of these proteins are starting to be revealed. These proteins have been implicated in targeting, trafficking to or from the membrane, desensitization, and fine-tuning of signaling.
引用
收藏
页码:553 / 572
页数:20
相关论文
共 162 条
[1]   Strategies for productring faster acting antidepressants [J].
Adell, A ;
Castro, E ;
Celeda, P ;
Bortolozzi, A ;
Pazos, A ;
Artigas, F .
DRUG DISCOVERY TODAY, 2005, 10 (08) :578-585
[2]   Serotonin, via 5-HT2A receptors, increases EPSCs in layer V pyramidal cells of prefrontal cortex by an asynchronous mode of glutamate release [J].
Aghajanian, GK ;
Marek, GJ .
BRAIN RESEARCH, 1999, 825 (1-2) :161-171
[3]  
Aghajanian GK, 1999, NEUROPSYCHOPHARMACOL, V21, pS16
[4]   Constitutive Gi2-dependent activation of adenylyl cyclase type II by the 5-HT1A receptor -: Inhibition by anxiolytic partial agonists [J].
Albert, PR ;
Sajedi, N ;
Lemonde, S ;
Ghahremani, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (50) :35469-35474
[5]   A-G PROTEIN COUPLES SEROTONIN AND GABA-B RECEPTORS TO THE SAME CHANNELS IN HIPPOCAMPUS [J].
ANDRADE, R ;
MALENKA, RC ;
NICOLL, RA .
SCIENCE, 1986, 234 (4781) :1261-1265
[6]  
ANDRADE R, 1991, J PHARMACOL EXP THER, V257, P930
[7]  
ANSANAY H, 1992, MOL PHARMACOL, V42, P808
[8]   CAMP-DEPENDENT, LONG-LASTING INHIBITION OF A K+ CURRENT IN MAMMALIAN NEURONS [J].
ANSANAY, H ;
DUMUIS, A ;
SEBBEN, M ;
BOCKAERT, J ;
FAGNI, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6635-6639
[9]   LSD and DOB:: interaction with 5-HT2A receptors to inhibit NMDA receptor-mediated transmission in the rat prefrontal cortex [J].
Arvanov, VL ;
Liang, XF ;
Russo, A ;
Wang, RY .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (09) :3064-3072
[10]   Deletion of the serotonin 5-HT2C receptor PDZ recognition motif prevents receptor phosphorylation and delays resensitization of receptor responses [J].
Backstrom, JR ;
Price, RD ;
Reasoner, DT ;
Sanders-Bush, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23620-23626