Bdnf gene is a downstream target of Nurr1 transcription factor in rat midbrain neurons in vitro

被引:80
作者
Volpicelli, Floriana [1 ]
Caiazzo, Massimiliano
Greco, Dario
Consales, Claudia
Leone, Luigi
Perrone-Capano, Carla
D'Amato, Luca Colucci
Di Porzio, Umberto
机构
[1] CNR, Inst Genet & Biophys A Buzzati Traverso, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Biol Sci, Naples, Italy
[3] Seconda Univ Napoli, Dept Life Sci, Caserta, Italy
关键词
DNA microarrays; luciferase assay; MAPK; protein kinase C; phospholipase C; siRNA;
D O I
10.1111/j.1471-4159.2007.04494.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factor Nurr1 is essential for the generation of midbrain dopaminergic neurons (mDA). Only a few Nurr1-regulated genes have so far been identified and it remains unclear how Nurr1 influences the development and function of dopaminergic neurons. To identify novel Nurr1 target genes we have used genome-wide expression profiling in rat midbrain primary cultures, enriched in dopaminergic neurons, following up-regulation of Nurr1 expression by depolarization. In this study we demonstrate that following depolarization the hyperexpression of Nurr1 and the brain derived neurotrophic factor (BDNF) are phospholipase C- and protein kinase C-dependent. We show that Bdnf, which encodes a neurotrophin involved also in the phenotypic maturation of mDA neurons, is a novel Nurr1 target gene. By RNA interference experiments we show that a decreased Nurr1 expression is followed by tyrosine hydroxylase and BDNF mRNA and protein down-regulation. Reporter gene assay experiments performed on midbrain primary cultures using four Bdnf promoter constructs show that Bdnf is a direct target gene of Nurr1. Taken together, our findings suggest that Nurr1 might also influence the development and the function of midbrain dopaminergic neurons via direct regulation of Bdnf expression.
引用
收藏
页码:441 / 453
页数:13
相关论文
共 75 条
[1]   The GDNF family: Signalling, biological functions and therapeutic value [J].
Airaksinen, MS ;
Saarma, M .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) :383-394
[2]   Engrailed genes are cell-autonomously required to prevent apoptosis in mesencephalic dopaminergic neurons [J].
Albéri, L ;
Sgadó, P ;
Simon, HH .
DEVELOPMENT, 2004, 131 (13) :3229-3236
[3]   BDNF gene transcripts in mesencephalic neurons and its differential regulation by NMDA [J].
Aliaga, E ;
Rage, F ;
Bustos, G ;
Tapia-Arancibia, L .
NEUROREPORT, 1998, 9 (09) :1959-1962
[4]  
Andersson E, 2006, CELL, V124, P393, DOI [10.1016/j.cell.2005.10.037, 10.1016/J.CELL.2005.10.037]
[5]   Maturation but not survival of dopaminergic nigrostriatal neurons is affected in developing and aging BDNF-deficient mice [J].
Baker, SA ;
Stanford, LE ;
Brown, RE ;
Hagg, T .
BRAIN RESEARCH, 2005, 1039 (1-2) :177-188
[6]   Transcription factors specifying dopamine phenotype are decreased in cocaine users [J].
Bannon, MJ ;
Pruetz, B ;
Barfield, E ;
Schmidt, CJ .
NEUROREPORT, 2004, 15 (03) :401-404
[7]   Decreased expression of the transcription factor NURR1 in dopamine neurons of cocaine abusers [J].
Bannon, MJ ;
Pruetz, B ;
Manning-Bog, AB ;
Whitty, CJ ;
Michelhaugh, SK ;
Sacchetti, P ;
Granneman, JG ;
Mash, DC ;
Schmidt, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) :6382-6385
[8]   Brain-derived neurotrophic factor is required for the establishment of the proper number of dopaminergic neurons in the substantia nigra pars compacta [J].
Baquet, ZC ;
Bickford, PC ;
Jones, KR .
JOURNAL OF NEUROSCIENCE, 2005, 25 (26) :6251-6259
[9]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[10]  
Buervenich S, 2000, AM J MED GENET, V96, P808, DOI 10.1002/1096-8628(20001204)96:6<808::AID-AJMG23>3.0.CO