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J Neurosci DOI:10.1523/JNEUROSCI.1732-12.2012

Normal midbrain dopaminergic neuron development and function in miR-133b mutant mice.

Publication TypeJournal Article
Year of Publication2012
AuthorsHeyer, MP, Pani, AK, Smeyne, RJ, Kenny, PJ, Feng, G
JournalJ Neurosci
Volume32
Issue32
Pages10887-94
Date Published2012 Aug 08
ISSN1529-2401
KeywordsAge Factors, Analysis of Variance, Animals, Animals, Newborn, Behavior, Animal, Cell Count, Choline O-Acetyltransferase, Chromatography, Liquid, Dark Adaptation, Dopamine, Dopaminergic Neurons, Electrochemical Techniques, Exploratory Behavior, Gene Expression Regulation, Developmental, Glutamate Decarboxylase, Homeodomain Proteins, Male, Maze Learning, Mesencephalon, Mice, Mice, Knockout, Mice, Neurologic Mutants, Microdialysis, MicroRNAs, Motor Activity, Psychomotor Performance, Stereotaxic Techniques, Transcription Factors, Tyrosine 3-Monooxygenase
Abstract

Midbrain dopaminergic (mDA) neurons control movement and emotion, and their degeneration leads to motor and cognitive defects in Parkinson's disease (PD). miR-133b is a conserved microRNA that is thought to regulate mDA neuron differentiation by targeting Pitx3, a transcription factor required for appropriate development of mDA substantia nigra neurons. Moreover, miR-133b has been found to be depleted in the midbrain of PD patients. However, the function of miR-133b in the intact midbrain has not been determined. Here we show that miR-133b null mice have normal numbers of mDA neurons during development and aging. Dopamine levels are unchanged in the striatum, while expression of dopaminergic genes, including Pitx3, is also unaffected. Finally, motor coordination and both spontaneous and psychostimulant-induced locomotion are unaltered in miR-133b null mice, suggesting that miR-133b does not play a significant role in mDA neuron development and maintenance in vivo.

DOI10.1523/JNEUROSCI.1732-12.2012
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/22875923?dopt=Abstract

Alternate JournalJ. Neurosci.
PubMed ID22875923
PubMed Central IDPMC3752074
Grant ListF31 NS063519 / NS / NINDS NIH HHS / United States