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Type: Journal article
Title: Locomotor hyperactivity in 14-3-3ζ KO mice is associated with dopamine transporter dysfunction
Other Titles: Locomotor hyperactivity in 14-3-3Zeta KO mice is associated with dopamine transporter dysfunction
Author: Ramshaw, H.
Xu, X.
Jaehne, E.
McCarthy, P.
Greenberg, Z.
Saleh, E.
McClure, B.
Woodcock, J.
Kabbara, S.
Wiszniak, S.
Wang, T.
Parish, C.
van den Buuse, M.
Baune, B.
Lopez, A.
Schwarz, Q.
Citation: Translational Psychiatry, 2013; 3(e327):1-10
Publisher: Nature Publishing Group
Issue Date: 2013
ISSN: 2158-3188
Organisation: Robinson Institute
Statement of
H Ramshaw, X Xu, EJ Jaehne, P McCarthy, Z Greenberg, E Saleh, B McClure, J Woodcock, S Kabbara, S Wiszniak, Ting-Yi Wang, C Parish, M van den Buuse, BT Baune, A Lopez and Q Schwarz
Abstract: 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 14-3-3ζ as an essential component of neurodevelopment and a central risk factor in the schizophrenia protein interaction network. Our analysis of 14-3-3ζ-deficient mice now shows that baseline hyperactivity of knockout (KO) mice is rescued by the antipsychotic drug clozapine. 14-3-3ζ KO mice displayed enhanced locomotor hyperactivity induced by the DA releaser amphetamine. Consistent with 14-3-3ζ having a role in DA signalling, we found increased levels of DA in the striatum of 14-3-3ζ KO mice. Although 14-3-3ζ 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 14-3-3ζ 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 14-3-3ζ controls DAT stability, we found a physical association between 14-3-3ζ and DAT by co-immunoprecipitation. Taken together, our results identify a novel role for 14-3-3ζ in DA neurotransmission and provide support to the hyperdopaminergic basis of pathologies associated with schizophrenia and related disorders.
Keywords: 14-3-3ζ
Dopamine neurotransmission
Dopamine transporter
Schizophrenia mouse model
Rights: ©2013 Macmillan Publishers Limited. This work is licensed under a Creative Commons Attribution- NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit
DOI: 10.1038/tp.2013.99
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