Abstract
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. © 2007 The Authors.
Original language | English |
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Pages (from-to) | 441-453 |
Number of pages | 13 |
Journal | Journal of Neurochemistry |
Volume | 102 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Jul 2007 |
Keywords
- DNA microarrays
- Luciferase assay
- MAPK
- Phospholipase C
- Protein kinase C
- siRNA
- brain derived neurotrophic factor
- messenger RNA
- neurotrophin
- nuclear receptor related factor 1
- phospholipase C
- protein kinase C
- tyrosine 3 monooxygenase
- animal cell
- animal cell culture
- article
- brain nerve cell
- cell maturation
- cell membrane depolarization
- controlled study
- dopaminergic nerve cell
- down regulation
- embryo
- gene expression profiling
- gene targeting
- genetic code
- genome analysis
- in vitro study
- mesencephalon
- microarray analysis
- nonhuman
- phenotype
- priority journal
- promoter region
- rat
- reporter gene
- reverse transcription polymerase chain reaction
- RNA interference
- RNA isolation
- upregulation
- Western blotting