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
[21]   GPCR-interacting proteins (GIPs):: nature and functions [J].
Bockaert, J ;
Roussignol, G ;
Bécamel, C ;
Gavarini, S ;
Joubert, L ;
Dumuis, A ;
Fagni, L ;
Marin, P .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2004, 32 :851-855
[22]   5-HT4 Receptors [J].
Bockaert, J. ;
Claeysen, S. ;
Compan, V ;
Dumuis, A. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2004, 3 (01) :39-51
[23]  
BOCKAERT J, 1990, MOL PHARMACOL, V37, P408
[24]   The 'magic tail' of G protein-coupled receptors: an anchorage for functional protein networks [J].
Bockaert, J ;
Marin, P ;
Dumuis, A ;
Fagni, L .
FEBS LETTERS, 2003, 546 (01) :65-72
[25]  
BOCKAERT J, 2005, MOL CELLULAR DETERMI
[26]  
BOCKAERT J, 1997, HDB EXPT PHARM SEROT, P439
[27]  
BOCKAERT J, 1998, LOCALIZATION 5 HT4 R
[28]   The serotonin system and spiritual experiences [J].
Borg, J ;
Andrée, B ;
Soderstrom, H ;
Farde, L .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (11) :1965-1969
[29]   5-HT1B RECEPTORS ARE NEGATIVELY COUPLED WITH ADENYLATE-CYCLASE IN RAT SUBSTANTIA NIGRA [J].
BOUHELAL, R ;
SMOUNYA, L ;
BOCKAERT, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 151 (02) :189-196
[30]   Localization of 5-HT6 receptors at the plasma membrane of neuronal cilia in the rat brain [J].
Brailov, I ;
Bancila, M ;
Brisorgueil, MJ ;
Miquel, MC ;
Hamon, M ;
Vergé, D .
BRAIN RESEARCH, 2000, 872 (1-2) :271-275