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Synaptic proteome changes in mouse brain regions upon auditory discrimination learning

Changes in synaptic efficacy underlying learning and memory processes are assumed to be associated with alterations of the protein composition of synapses. Here, we performed a quantitative proteomic screen to monitor changes in the synaptic proteome of four brain areas (auditory cortex, frontal cor...

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Autores principales: Kähne, Thilo, Kolodziej, Angela, Smalla, Karl-Heinz, Eisenschmidt, Elke, Haus, Utz-Uwe, Weismantel, Robert, Kropf, Siegfried, Wetzel, Wolfram, Ohl, Frank W., Tischmeyer, Wolfgang, Naumann, Michael, Gundelfinger, Eckart D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag GmbH & Co. KGaA 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509369/
https://www.ncbi.nlm.nih.gov/pubmed/22696468
http://dx.doi.org/10.1002/pmic.201100669
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author Kähne, Thilo
Kolodziej, Angela
Smalla, Karl-Heinz
Eisenschmidt, Elke
Haus, Utz-Uwe
Weismantel, Robert
Kropf, Siegfried
Wetzel, Wolfram
Ohl, Frank W.
Tischmeyer, Wolfgang
Naumann, Michael
Gundelfinger, Eckart D.
author_facet Kähne, Thilo
Kolodziej, Angela
Smalla, Karl-Heinz
Eisenschmidt, Elke
Haus, Utz-Uwe
Weismantel, Robert
Kropf, Siegfried
Wetzel, Wolfram
Ohl, Frank W.
Tischmeyer, Wolfgang
Naumann, Michael
Gundelfinger, Eckart D.
author_sort Kähne, Thilo
collection PubMed
description Changes in synaptic efficacy underlying learning and memory processes are assumed to be associated with alterations of the protein composition of synapses. Here, we performed a quantitative proteomic screen to monitor changes in the synaptic proteome of four brain areas (auditory cortex, frontal cortex, hippocampus striatum) during auditory learning. Mice were trained in a shuttle box GO/NO-GO paradigm to discriminate between rising and falling frequency modulated tones to avoid mild electric foot shock. Control-treated mice received corresponding numbers of either the tones or the foot shocks. Six hours and 24 h later, the composition of a fraction enriched in synaptic cytomatrix-associated proteins was compared to that obtained from naïve mice by quantitative mass spectrometry. In the synaptic protein fraction obtained from trained mice, the average percentage (±SEM) of downregulated proteins (59.9 ± 0.5%) exceeded that of upregulated proteins (23.5 ± 0.8%) in the brain regions studied. This effect was significantly smaller in foot shock (42.7 ± 0.6% down, 40.7 ± 1.0% up) and tone controls (43.9 ± 1.0% down, 39.7 ± 0.9% up). These data suggest that learning processes initially induce removal and/or degradation of proteins from presynaptic and postsynaptic cytoskeletal matrices before these structures can acquire a new, postlearning organisation. In silico analysis points to a general role of insulin-like signalling in this process.
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spelling pubmed-35093692012-12-06 Synaptic proteome changes in mouse brain regions upon auditory discrimination learning Kähne, Thilo Kolodziej, Angela Smalla, Karl-Heinz Eisenschmidt, Elke Haus, Utz-Uwe Weismantel, Robert Kropf, Siegfried Wetzel, Wolfram Ohl, Frank W. Tischmeyer, Wolfgang Naumann, Michael Gundelfinger, Eckart D. Proteomics Research Articles Changes in synaptic efficacy underlying learning and memory processes are assumed to be associated with alterations of the protein composition of synapses. Here, we performed a quantitative proteomic screen to monitor changes in the synaptic proteome of four brain areas (auditory cortex, frontal cortex, hippocampus striatum) during auditory learning. Mice were trained in a shuttle box GO/NO-GO paradigm to discriminate between rising and falling frequency modulated tones to avoid mild electric foot shock. Control-treated mice received corresponding numbers of either the tones or the foot shocks. Six hours and 24 h later, the composition of a fraction enriched in synaptic cytomatrix-associated proteins was compared to that obtained from naïve mice by quantitative mass spectrometry. In the synaptic protein fraction obtained from trained mice, the average percentage (±SEM) of downregulated proteins (59.9 ± 0.5%) exceeded that of upregulated proteins (23.5 ± 0.8%) in the brain regions studied. This effect was significantly smaller in foot shock (42.7 ± 0.6% down, 40.7 ± 1.0% up) and tone controls (43.9 ± 1.0% down, 39.7 ± 0.9% up). These data suggest that learning processes initially induce removal and/or degradation of proteins from presynaptic and postsynaptic cytoskeletal matrices before these structures can acquire a new, postlearning organisation. In silico analysis points to a general role of insulin-like signalling in this process. WILEY-VCH Verlag GmbH & Co. KGaA 2012-08 2012-08-20 /pmc/articles/PMC3509369/ /pubmed/22696468 http://dx.doi.org/10.1002/pmic.201100669 Text en © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Kähne, Thilo
Kolodziej, Angela
Smalla, Karl-Heinz
Eisenschmidt, Elke
Haus, Utz-Uwe
Weismantel, Robert
Kropf, Siegfried
Wetzel, Wolfram
Ohl, Frank W.
Tischmeyer, Wolfgang
Naumann, Michael
Gundelfinger, Eckart D.
Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title_full Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title_fullStr Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title_full_unstemmed Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title_short Synaptic proteome changes in mouse brain regions upon auditory discrimination learning
title_sort synaptic proteome changes in mouse brain regions upon auditory discrimination learning
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509369/
https://www.ncbi.nlm.nih.gov/pubmed/22696468
http://dx.doi.org/10.1002/pmic.201100669
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