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Publication : Locomotor hyperactivity in 14-3-3ΞΆ KO mice is associated with dopamine transporter dysfunction.

First Author  Ramshaw H Year  2013
Journal  Transl Psychiatry Volume  3
Pages  e327 PubMed ID  24301645
Mgi Jnum  J:250077 Mgi Id  MGI:6101538
Doi  10.1038/tp.2013.99 Citation  Ramshaw H, et al. (2013) Locomotor hyperactivity in 14-3-3zeta KO mice is associated with dopamine transporter dysfunction. Transl Psychiatry 3:e327
abstractText  Dopamine (DA) neurotransmission requires a complex series of enzymatic reactions that are tightly linked to catecholamine exocytosis and receptor interactions on pre- and postsynaptic neurons. Regulation of dopaminergic signalling is primarily achieved through reuptake of extracellular DA by the DA transporter (DAT) on presynaptic neurons. Aberrant regulation of DA signalling, and in particular hyperactivation, has been proposed as a key insult in the presentation of schizophrenia and related neuropsychiatric disorders. We recently identified 14-3-3zeta as an essential component of neurodevelopment and a central risk factor in the schizophrenia protein interaction network. Our analysis of 14-3-3zeta-deficient mice now shows that baseline hyperactivity of knockout (KO) mice is rescued by the antipsychotic drug clozapine. 14-3-3zeta KO mice displayed enhanced locomotor hyperactivity induced by the DA releaser amphetamine. Consistent with 14-3-3zeta having a role in DA signalling, we found increased levels of DA in the striatum of 14-3-3zeta KO mice. Although 14-3-3zeta is proposed to modulate activity of the rate-limiting DA biosynthesis enzyme, tyrosine hydroxylase (TH), we were unable to identify any differences in total TH levels, TH localization or TH activation in 14-3-3zeta KO mice. Rather, our analysis identified significantly reduced levels of DAT in the absence of notable differences in RNA or protein levels of DA receptors D1-D5. Providing insight into the mechanisms by which 14-3-3zeta controls DAT stability, we found a physical association between 14-3-3zeta and DAT by co-immunoprecipitation. Taken together, our results identify a novel role for 14-3-3zeta in DA neurotransmission and provide support to the hyperdopaminergic basis of pathologies associated with schizophrenia and related disorders.
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