author_facet Xiong, Hui
Cassé, Frédéric
Zhou, Yang
Zhou, Ming
Xiong, Zhi-Qi
Joëls, Marian
Martin, Stéphane
Krugers, Harm J.
Xiong, Hui
Cassé, Frédéric
Zhou, Yang
Zhou, Ming
Xiong, Zhi-Qi
Joëls, Marian
Martin, Stéphane
Krugers, Harm J.
author Xiong, Hui
Cassé, Frédéric
Zhou, Yang
Zhou, Ming
Xiong, Zhi-Qi
Joëls, Marian
Martin, Stéphane
Krugers, Harm J.
spellingShingle Xiong, Hui
Cassé, Frédéric
Zhou, Yang
Zhou, Ming
Xiong, Zhi-Qi
Joëls, Marian
Martin, Stéphane
Krugers, Harm J.
Learning & Memory
mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
Cellular and Molecular Neuroscience
Cognitive Neuroscience
Neuropsychology and Physiological Psychology
author_sort xiong, hui
spelling Xiong, Hui Cassé, Frédéric Zhou, Yang Zhou, Ming Xiong, Zhi-Qi Joëls, Marian Martin, Stéphane Krugers, Harm J. 1549-5485 Cold Spring Harbor Laboratory Cellular and Molecular Neuroscience Cognitive Neuroscience Neuropsychology and Physiological Psychology http://dx.doi.org/10.1101/lm.039420.115 <jats:p>Glucocorticoid hormones, via activation of their receptors, promote memory consolidation, but the exact underlying mechanisms remain elusive. We examined how corticosterone regulates AMPA receptors (AMPARs), which are crucial for synaptic plasticity and memory formation. Combining a live imaging fluorescent recovery after photobleaching approach with the use of the pH-sensitive GFP-AMPAR tagging revealed that corticosterone enhances the AMPAR mobile fraction and increases synaptic trapping of AMPARs in hippocampal cells. In parallel, corticosterone-enhanced AMPAR-mediated synaptic transmission. Blocking the mammalian target of rapamycin (mTOR) pathway prevented the effects of corticosterone on both AMPAR trapping—but not on the mobile fraction—and synaptic transmission. Blocking the mTOR pathway also prevented the memory enhancing effects of corticosterone in a contextual fear-conditioning paradigm. We conclude that activation of the mTOR pathway is essential for the effects of corticosterone on synaptic trapping of AMPARs and, possibly as a consequence, fearful memory formation.</jats:p> mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory Learning & Memory
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title mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_unstemmed mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_full mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_fullStr mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_full_unstemmed mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_short mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_sort mtor is essential for corticosteroid effects on hippocampal ampa receptor function and fear memory
topic Cellular and Molecular Neuroscience
Cognitive Neuroscience
Neuropsychology and Physiological Psychology
url http://dx.doi.org/10.1101/lm.039420.115
publishDate 2015
physical 577-583
description <jats:p>Glucocorticoid hormones, via activation of their receptors, promote memory consolidation, but the exact underlying mechanisms remain elusive. We examined how corticosterone regulates AMPA receptors (AMPARs), which are crucial for synaptic plasticity and memory formation. Combining a live imaging fluorescent recovery after photobleaching approach with the use of the pH-sensitive GFP-AMPAR tagging revealed that corticosterone enhances the AMPAR mobile fraction and increases synaptic trapping of AMPARs in hippocampal cells. In parallel, corticosterone-enhanced AMPAR-mediated synaptic transmission. Blocking the mammalian target of rapamycin (mTOR) pathway prevented the effects of corticosterone on both AMPAR trapping—but not on the mobile fraction—and synaptic transmission. Blocking the mTOR pathway also prevented the memory enhancing effects of corticosterone in a contextual fear-conditioning paradigm. We conclude that activation of the mTOR pathway is essential for the effects of corticosterone on synaptic trapping of AMPARs and, possibly as a consequence, fearful memory formation.</jats:p>
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author Xiong, Hui, Cassé, Frédéric, Zhou, Yang, Zhou, Ming, Xiong, Zhi-Qi, Joëls, Marian, Martin, Stéphane, Krugers, Harm J.
author_facet Xiong, Hui, Cassé, Frédéric, Zhou, Yang, Zhou, Ming, Xiong, Zhi-Qi, Joëls, Marian, Martin, Stéphane, Krugers, Harm J., Xiong, Hui, Cassé, Frédéric, Zhou, Yang, Zhou, Ming, Xiong, Zhi-Qi, Joëls, Marian, Martin, Stéphane, Krugers, Harm J.
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description <jats:p>Glucocorticoid hormones, via activation of their receptors, promote memory consolidation, but the exact underlying mechanisms remain elusive. We examined how corticosterone regulates AMPA receptors (AMPARs), which are crucial for synaptic plasticity and memory formation. Combining a live imaging fluorescent recovery after photobleaching approach with the use of the pH-sensitive GFP-AMPAR tagging revealed that corticosterone enhances the AMPAR mobile fraction and increases synaptic trapping of AMPARs in hippocampal cells. In parallel, corticosterone-enhanced AMPAR-mediated synaptic transmission. Blocking the mammalian target of rapamycin (mTOR) pathway prevented the effects of corticosterone on both AMPAR trapping—but not on the mobile fraction—and synaptic transmission. Blocking the mTOR pathway also prevented the memory enhancing effects of corticosterone in a contextual fear-conditioning paradigm. We conclude that activation of the mTOR pathway is essential for the effects of corticosterone on synaptic trapping of AMPARs and, possibly as a consequence, fearful memory formation.</jats:p>
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spelling Xiong, Hui Cassé, Frédéric Zhou, Yang Zhou, Ming Xiong, Zhi-Qi Joëls, Marian Martin, Stéphane Krugers, Harm J. 1549-5485 Cold Spring Harbor Laboratory Cellular and Molecular Neuroscience Cognitive Neuroscience Neuropsychology and Physiological Psychology http://dx.doi.org/10.1101/lm.039420.115 <jats:p>Glucocorticoid hormones, via activation of their receptors, promote memory consolidation, but the exact underlying mechanisms remain elusive. We examined how corticosterone regulates AMPA receptors (AMPARs), which are crucial for synaptic plasticity and memory formation. Combining a live imaging fluorescent recovery after photobleaching approach with the use of the pH-sensitive GFP-AMPAR tagging revealed that corticosterone enhances the AMPAR mobile fraction and increases synaptic trapping of AMPARs in hippocampal cells. In parallel, corticosterone-enhanced AMPAR-mediated synaptic transmission. Blocking the mammalian target of rapamycin (mTOR) pathway prevented the effects of corticosterone on both AMPAR trapping—but not on the mobile fraction—and synaptic transmission. Blocking the mTOR pathway also prevented the memory enhancing effects of corticosterone in a contextual fear-conditioning paradigm. We conclude that activation of the mTOR pathway is essential for the effects of corticosterone on synaptic trapping of AMPARs and, possibly as a consequence, fearful memory formation.</jats:p> mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory Learning & Memory
spellingShingle Xiong, Hui, Cassé, Frédéric, Zhou, Yang, Zhou, Ming, Xiong, Zhi-Qi, Joëls, Marian, Martin, Stéphane, Krugers, Harm J., Learning & Memory, mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory, Cellular and Molecular Neuroscience, Cognitive Neuroscience, Neuropsychology and Physiological Psychology
title mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_full mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_fullStr mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_full_unstemmed mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_short mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
title_sort mtor is essential for corticosteroid effects on hippocampal ampa receptor function and fear memory
title_unstemmed mTOR is essential for corticosteroid effects on hippocampal AMPA receptor function and fear memory
topic Cellular and Molecular Neuroscience, Cognitive Neuroscience, Neuropsychology and Physiological Psychology
url http://dx.doi.org/10.1101/lm.039420.115