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Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L

Exercise is a potent enhancer of learning and memory, yet we know little of the underlying mechanisms that likely include alterations in synaptic efficacy in the hippocampus. To address this issue, we exposed mice to a single episode of voluntary exercise, and permanently marked activated mature hip...

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Autores principales: Chatzi, Christina, Zhang, Yingyu, Hendricks, Wiiliam D, Chen, Yang, Schnell, Eric, Goodman, Richard H, Westbrook, Gary L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609409/
https://www.ncbi.nlm.nih.gov/pubmed/31232686
http://dx.doi.org/10.7554/eLife.45920
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author Chatzi, Christina
Zhang, Yingyu
Hendricks, Wiiliam D
Chen, Yang
Schnell, Eric
Goodman, Richard H
Westbrook, Gary L
author_facet Chatzi, Christina
Zhang, Yingyu
Hendricks, Wiiliam D
Chen, Yang
Schnell, Eric
Goodman, Richard H
Westbrook, Gary L
author_sort Chatzi, Christina
collection PubMed
description Exercise is a potent enhancer of learning and memory, yet we know little of the underlying mechanisms that likely include alterations in synaptic efficacy in the hippocampus. To address this issue, we exposed mice to a single episode of voluntary exercise, and permanently marked activated mature hippocampal dentate granule cells using conditional Fos-TRAP mice. Exercise-activated neurons (Fos-TRAPed) showed an input-selective increase in dendritic spines and excitatory postsynaptic currents at 3 days post-exercise, indicative of exercise-induced structural plasticity. Laser-capture microdissection and RNASeq of activated neurons revealed that the most highly induced transcript was Mtss1L, a little-studied I-BAR domain-containing gene, which we hypothesized could be involved in membrane curvature and dendritic spine formation. shRNA-mediated Mtss1L knockdown in vivo prevented the exercise-induced increases in spines and excitatory postsynaptic currents. Our results link short-term effects of exercise to activity-dependent expression of Mtss1L, which we propose as a novel effector of activity-dependent rearrangement of synapses.
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spelling pubmed-66094092019-07-08 Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L Chatzi, Christina Zhang, Yingyu Hendricks, Wiiliam D Chen, Yang Schnell, Eric Goodman, Richard H Westbrook, Gary L eLife Neuroscience Exercise is a potent enhancer of learning and memory, yet we know little of the underlying mechanisms that likely include alterations in synaptic efficacy in the hippocampus. To address this issue, we exposed mice to a single episode of voluntary exercise, and permanently marked activated mature hippocampal dentate granule cells using conditional Fos-TRAP mice. Exercise-activated neurons (Fos-TRAPed) showed an input-selective increase in dendritic spines and excitatory postsynaptic currents at 3 days post-exercise, indicative of exercise-induced structural plasticity. Laser-capture microdissection and RNASeq of activated neurons revealed that the most highly induced transcript was Mtss1L, a little-studied I-BAR domain-containing gene, which we hypothesized could be involved in membrane curvature and dendritic spine formation. shRNA-mediated Mtss1L knockdown in vivo prevented the exercise-induced increases in spines and excitatory postsynaptic currents. Our results link short-term effects of exercise to activity-dependent expression of Mtss1L, which we propose as a novel effector of activity-dependent rearrangement of synapses. eLife Sciences Publications, Ltd 2019-06-24 /pmc/articles/PMC6609409/ /pubmed/31232686 http://dx.doi.org/10.7554/eLife.45920 Text en © 2019, Chatzi et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Chatzi, Christina
Zhang, Yingyu
Hendricks, Wiiliam D
Chen, Yang
Schnell, Eric
Goodman, Richard H
Westbrook, Gary L
Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title_full Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title_fullStr Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title_full_unstemmed Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title_short Exercise-induced enhancement of synaptic function triggered by the inverse BAR protein, Mtss1L
title_sort exercise-induced enhancement of synaptic function triggered by the inverse bar protein, mtss1l
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609409/
https://www.ncbi.nlm.nih.gov/pubmed/31232686
http://dx.doi.org/10.7554/eLife.45920
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