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A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice

BACKGROUND: Parkinson's disease (PD), the second most frequent neurodegenerative disorder at old age, can be caused by elevated expression or the A53T missense mutation of the presynaptic protein alpha-synuclein (SNCA). PD is characterized pathologically by the preferential vulnerability of the...

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Autores principales: Kurz, Alexander, Double, Kay L., Lastres-Becker, Isabel, Tozzi, Alessandro, Tantucci, Michela, Bockhart, Vanessa, Bonin, Michael, García-Arencibia, Moisés, Nuber, Silke, Schlaudraff, Falk, Liss, Birgit, Fernández-Ruiz, Javier, Gerlach, Manfred, Wüllner, Ullrich, Lüddens, Hartmut, Calabresi, Paolo, Auburger, Georg, Gispert, Suzana
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898885/
https://www.ncbi.nlm.nih.gov/pubmed/20628651
http://dx.doi.org/10.1371/journal.pone.0011464
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author Kurz, Alexander
Double, Kay L.
Lastres-Becker, Isabel
Tozzi, Alessandro
Tantucci, Michela
Bockhart, Vanessa
Bonin, Michael
García-Arencibia, Moisés
Nuber, Silke
Schlaudraff, Falk
Liss, Birgit
Fernández-Ruiz, Javier
Gerlach, Manfred
Wüllner, Ullrich
Lüddens, Hartmut
Calabresi, Paolo
Auburger, Georg
Gispert, Suzana
author_facet Kurz, Alexander
Double, Kay L.
Lastres-Becker, Isabel
Tozzi, Alessandro
Tantucci, Michela
Bockhart, Vanessa
Bonin, Michael
García-Arencibia, Moisés
Nuber, Silke
Schlaudraff, Falk
Liss, Birgit
Fernández-Ruiz, Javier
Gerlach, Manfred
Wüllner, Ullrich
Lüddens, Hartmut
Calabresi, Paolo
Auburger, Georg
Gispert, Suzana
author_sort Kurz, Alexander
collection PubMed
description BACKGROUND: Parkinson's disease (PD), the second most frequent neurodegenerative disorder at old age, can be caused by elevated expression or the A53T missense mutation of the presynaptic protein alpha-synuclein (SNCA). PD is characterized pathologically by the preferential vulnerability of the dopaminergic nigrostriatal projection neurons. METHODOLOGY/PRINCIPAL FINDINGS: Here, we used two mouse lines overexpressing human A53T-SNCA and studied striatal dysfunction in the absence of neurodegeneration to understand early disease mechanisms. To characterize the progression, we employed young adult as well as old mice. Analysis of striatal neurotransmitter content demonstrated that dopamine (DA) levels correlated directly with the level of expression of SNCA, an observation also made in SNCA-deficient (knockout, KO) mice. However, the elevated DA levels in the striatum of old A53T-SNCA overexpressing mice may not be transmitted appropriately, in view of three observations. First, a transcriptional downregulation of the extraneural DA degradation enzyme catechol-ortho-methytransferase (COMT) was found. Second, an upregulation of DA receptors was detected by immunoblots and autoradiography. Third, extensive transcriptome studies via microarrays and quantitative real-time RT-PCR (qPCR) of altered transcript levels of the DA-inducible genes Atf2, Cb(1), Freq, Homer1 and Pde7b indicated a progressive and genotype-dependent reduction in the postsynaptic DA response. As a functional consequence, long term depression (LTD) was absent in corticostriatal slices from old transgenic mice. CONCLUSIONS/SIGNIFICANCE: Taken together, the dysfunctional neurotransmission and impaired synaptic plasticity seen in the A53T-SNCA overexpressing mice reflect early changes within the basal ganglia prior to frank neurodegeneration. As a model of preclinical stages of PD, such insights may help to develop neuroprotective therapeutic approaches.
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spelling pubmed-28988852010-07-13 A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice Kurz, Alexander Double, Kay L. Lastres-Becker, Isabel Tozzi, Alessandro Tantucci, Michela Bockhart, Vanessa Bonin, Michael García-Arencibia, Moisés Nuber, Silke Schlaudraff, Falk Liss, Birgit Fernández-Ruiz, Javier Gerlach, Manfred Wüllner, Ullrich Lüddens, Hartmut Calabresi, Paolo Auburger, Georg Gispert, Suzana PLoS One Research Article BACKGROUND: Parkinson's disease (PD), the second most frequent neurodegenerative disorder at old age, can be caused by elevated expression or the A53T missense mutation of the presynaptic protein alpha-synuclein (SNCA). PD is characterized pathologically by the preferential vulnerability of the dopaminergic nigrostriatal projection neurons. METHODOLOGY/PRINCIPAL FINDINGS: Here, we used two mouse lines overexpressing human A53T-SNCA and studied striatal dysfunction in the absence of neurodegeneration to understand early disease mechanisms. To characterize the progression, we employed young adult as well as old mice. Analysis of striatal neurotransmitter content demonstrated that dopamine (DA) levels correlated directly with the level of expression of SNCA, an observation also made in SNCA-deficient (knockout, KO) mice. However, the elevated DA levels in the striatum of old A53T-SNCA overexpressing mice may not be transmitted appropriately, in view of three observations. First, a transcriptional downregulation of the extraneural DA degradation enzyme catechol-ortho-methytransferase (COMT) was found. Second, an upregulation of DA receptors was detected by immunoblots and autoradiography. Third, extensive transcriptome studies via microarrays and quantitative real-time RT-PCR (qPCR) of altered transcript levels of the DA-inducible genes Atf2, Cb(1), Freq, Homer1 and Pde7b indicated a progressive and genotype-dependent reduction in the postsynaptic DA response. As a functional consequence, long term depression (LTD) was absent in corticostriatal slices from old transgenic mice. CONCLUSIONS/SIGNIFICANCE: Taken together, the dysfunctional neurotransmission and impaired synaptic plasticity seen in the A53T-SNCA overexpressing mice reflect early changes within the basal ganglia prior to frank neurodegeneration. As a model of preclinical stages of PD, such insights may help to develop neuroprotective therapeutic approaches. Public Library of Science 2010-07-07 /pmc/articles/PMC2898885/ /pubmed/20628651 http://dx.doi.org/10.1371/journal.pone.0011464 Text en Kurz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kurz, Alexander
Double, Kay L.
Lastres-Becker, Isabel
Tozzi, Alessandro
Tantucci, Michela
Bockhart, Vanessa
Bonin, Michael
García-Arencibia, Moisés
Nuber, Silke
Schlaudraff, Falk
Liss, Birgit
Fernández-Ruiz, Javier
Gerlach, Manfred
Wüllner, Ullrich
Lüddens, Hartmut
Calabresi, Paolo
Auburger, Georg
Gispert, Suzana
A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title_full A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title_fullStr A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title_full_unstemmed A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title_short A53T-Alpha-Synuclein Overexpression Impairs Dopamine Signaling and Striatal Synaptic Plasticity in Old Mice
title_sort a53t-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898885/
https://www.ncbi.nlm.nih.gov/pubmed/20628651
http://dx.doi.org/10.1371/journal.pone.0011464
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