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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag GmbH & Co. KGaA
2012
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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. |
format | Online Article Text |
id | pubmed-3509369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | WILEY-VCH Verlag GmbH & Co. KGaA |
record_format | MEDLINE/PubMed |
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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