Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783432312658067456 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6609409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chatzichristina exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT zhangyingyu exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT hendrickswiiliamd exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT chenyang exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT schnelleric exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT goodmanrichardh exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l AT westbrookgaryl exerciseinducedenhancementofsynapticfunctiontriggeredbytheinversebarproteinmtss1l |