Role of p11 in Cellular and Behavioral Effects of 5-HT4 Receptor Stimulation

被引:132
作者
Warner-Schmidt, Jennifer L. [1 ]
Flajolet, Marc [1 ]
Maller, Abigail [1 ]
Chen, Emily Y. [1 ]
Qi, Hongshi [2 ]
Svenningsson, Per [1 ,2 ]
Greengard, Paul [1 ]
机构
[1] Rockefeller Univ, Mol & Cellular Neurosci Lab, New York, NY 10065 USA
[2] Karolinska Inst, Dept Physiol & Pharmacol, Ctr Mol Med, SE-17177 Stockholm, Sweden
关键词
antidepressant; depression; RS67333; S100A10; serotonin receptor; agonist; SEROTONIN RECEPTORS; NUCLEUS-ACCUMBENS; GENE-EXPRESSION; NERVOUS-SYSTEM; ACTIVATION; BRAIN; ANTIDEPRESSANTS; DEPRESSION; NEURONS; PROTEIN;
D O I
10.1523/JNEUROSCI.5343-08.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
p11 (S100A10), a member of a large family of S100 proteins, interacts with serotonin receptor 1B (5-HTR1B), modulates 5-HT1B receptor signal transduction, and is required for antidepressant responses to activation of this receptor. In the current study, we investigated the specificity of the interaction between 5-HTR1B and p11 by screening brain-expressed S100 proteins against serotonin and noradrenergic receptors. The data indicate that p11 is unique among its family members for its interactions with defined serotonin receptors. We identify a novel p11-interacting receptor (5-HTR4) and characterize the interaction between p11 and 5-HTR4, demonstrating that (1) p11 and 5-HTR4 mRNA and protein are coexpressed in brain regions that are relevant for major depression, (2) p11 increases 5-HTR4 surface expression and facilitates 5-HTR4 signaling, and (3) p11 is required for the behavioral antidepressant responses to 5-HTR4 stimulation in vivo. The essential role played by p11 in modulating signaling through 5-HT4 as well as 5-HT1B receptors supports the concept that this protein may be a key determinant of vulnerability to depression.
引用
收藏
页码:1937 / 1946
页数:10
相关论文
共 32 条
[1]   A compendium of specific motifs for diagnosing GPCR subtypes [J].
Attwood, TK .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (04) :162-165
[2]   A review of central 5-HT receptors and their function [J].
Barnes, NM ;
Sharp, T .
NEUROPHARMACOLOGY, 1999, 38 (08) :1083-1152
[3]   5-Hydroxytryptamine4 receptor activation of the extracellular signal-regulated kinase pathway depends on src activation but not on G protein or β-arrestin signaling [J].
Barthet, Gael ;
Framery, Berenice ;
Gaven, Florence ;
Pellissier, Lucie ;
Reiter, Eric ;
Claeysen, Sylvie ;
Bockaert, Joel ;
Dumuis, Aline .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (06) :1979-1991
[4]   Preferential expression of 5-HT1D over 5-HT1B receptors during early embryogenesis [J].
BolanosJimenez, F ;
Choi, DS ;
Maroteaux, L .
NEUROREPORT, 1997, 8 (17) :3655-3660
[5]   LOCALIZATION OF 5-HT1B, 5-HT1D-ALPHA, 5-HT1E AND 5-HT1F, RECEPTOR MESSENGER-RNA IN RODENT AND PRIMATE BRAIN [J].
BRUINVELS, AT ;
LANDWEHRMEYER, B ;
GUSTAFSON, EL ;
DURKIN, MM ;
MENGOD, G ;
BRANCHEK, TA ;
HOYER, D ;
PALACIOS, JM .
NEUROPHARMACOLOGY, 1994, 33 (3-4) :367-386
[6]   Attenuated response to stress and novelty and hypersensitivity to seizures in 5-HT4 receptor knock-out mice [J].
Compan, V ;
Zhou, MM ;
Grailhe, R ;
Gazzara, RA ;
Martin, R ;
Gingrich, J ;
Dumuis, A ;
Brunner, D ;
Bockaert, J ;
Hen, R .
JOURNAL OF NEUROSCIENCE, 2004, 24 (02) :412-419
[7]   Assessing antidepressant activity in rodents: recent developments and future needs [J].
Cryan, JF ;
Markou, A ;
Lucki, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (05) :238-245
[8]   Functional roles of S100 proteins, calcium-binding proteins of the EF-hand type [J].
Donato, R .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1999, 1450 (03) :191-231
[9]   PHARMACOLOGICAL CHARACTERIZATION OF 2 NOVEL AND POTENT 5-HT4 RECEPTOR AGONISTS, RS-67333 AND RS-67506, IN-VITRO AND IN-VIVO [J].
EGLEN, RM ;
BONHAUS, DW ;
JOHNSON, LG ;
LEUNG, E ;
CLARK, RD .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 115 (08) :1387-1392
[10]  
EGLEN RM, 1995, TRENDS PHARMACOL SCI, V16, P391, DOI 10.1016/S0165-6147(00)89081-1