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mTOR signaling contributes to motor skill learning in mice
The mammalian target of rapamycin (mTOR) kinase is a critical regulator of mRNA translation and is suspected to be involved in various long-lasting forms of synaptic and behavioral plasticity. However, its role in motor learning and control has never been examined. This study investigated, in mice,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982074/ https://www.ncbi.nlm.nih.gov/pubmed/24772063 http://dx.doi.org/10.3389/fnmol.2014.00026 |
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author | Bergeron, Yan Chagniel, Laure Bureau, Geneviève Massicotte, Guy Cyr, Michel |
author_facet | Bergeron, Yan Chagniel, Laure Bureau, Geneviève Massicotte, Guy Cyr, Michel |
author_sort | Bergeron, Yan |
collection | PubMed |
description | The mammalian target of rapamycin (mTOR) kinase is a critical regulator of mRNA translation and is suspected to be involved in various long-lasting forms of synaptic and behavioral plasticity. However, its role in motor learning and control has never been examined. This study investigated, in mice, the implication of mTOR in the learning processes associated with the accelerating rotarod task. We first observed that the rotarod learning did not alter the levels of total mTOR in the striatum, hippocampus, cerebellum, and anterior cortex of trained mice. However, it increased the levels of phosphorylated mTOR in the striatum and hippocampus exclusively during the first session of training; no change was observed at the second and third sessions. In order to further investigate the potential role of mTOR during motor skill learning, we performed systemic and intrastriatal inhibitions of mTOR using the pharmacological inhibitor rapamycin, as well as a genetic knockdown of striatal mTOR using intrastriatal infusion of mTOR siRNA. These three independent approaches were all associated with a significant reduction in rotarod performances that were reminiscent of impaired consolidation processes. Notably, these treatments did not affect the capacity of mice to execute the pole test, suggesting that mTOR activity was mainly controlling motor learning rather than motor abilities. Moreover, all treatments decreased the levels of phosphorylated 4EBP1 and P70S6K, two molecular downstream targets of mTORC1. Our findings demonstrate that striatal mTOR kinase, via the phosphorylation of 4EBP1 and P70S6K, plays an important role in the cellular and molecular processes involved in motor skill learning. |
format | Online Article Text |
id | pubmed-3982074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39820742014-04-25 mTOR signaling contributes to motor skill learning in mice Bergeron, Yan Chagniel, Laure Bureau, Geneviève Massicotte, Guy Cyr, Michel Front Mol Neurosci Neuroscience The mammalian target of rapamycin (mTOR) kinase is a critical regulator of mRNA translation and is suspected to be involved in various long-lasting forms of synaptic and behavioral plasticity. However, its role in motor learning and control has never been examined. This study investigated, in mice, the implication of mTOR in the learning processes associated with the accelerating rotarod task. We first observed that the rotarod learning did not alter the levels of total mTOR in the striatum, hippocampus, cerebellum, and anterior cortex of trained mice. However, it increased the levels of phosphorylated mTOR in the striatum and hippocampus exclusively during the first session of training; no change was observed at the second and third sessions. In order to further investigate the potential role of mTOR during motor skill learning, we performed systemic and intrastriatal inhibitions of mTOR using the pharmacological inhibitor rapamycin, as well as a genetic knockdown of striatal mTOR using intrastriatal infusion of mTOR siRNA. These three independent approaches were all associated with a significant reduction in rotarod performances that were reminiscent of impaired consolidation processes. Notably, these treatments did not affect the capacity of mice to execute the pole test, suggesting that mTOR activity was mainly controlling motor learning rather than motor abilities. Moreover, all treatments decreased the levels of phosphorylated 4EBP1 and P70S6K, two molecular downstream targets of mTORC1. Our findings demonstrate that striatal mTOR kinase, via the phosphorylation of 4EBP1 and P70S6K, plays an important role in the cellular and molecular processes involved in motor skill learning. Frontiers Media S.A. 2014-04-03 /pmc/articles/PMC3982074/ /pubmed/24772063 http://dx.doi.org/10.3389/fnmol.2014.00026 Text en Copyright © 2014 Bergeron, Chagniel, Bureau, Massicotte and Cyr. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Bergeron, Yan Chagniel, Laure Bureau, Geneviève Massicotte, Guy Cyr, Michel mTOR signaling contributes to motor skill learning in mice |
title | mTOR signaling contributes to motor skill learning in mice |
title_full | mTOR signaling contributes to motor skill learning in mice |
title_fullStr | mTOR signaling contributes to motor skill learning in mice |
title_full_unstemmed | mTOR signaling contributes to motor skill learning in mice |
title_short | mTOR signaling contributes to motor skill learning in mice |
title_sort | mtor signaling contributes to motor skill learning in mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982074/ https://www.ncbi.nlm.nih.gov/pubmed/24772063 http://dx.doi.org/10.3389/fnmol.2014.00026 |
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