Cargando…
Cortical Up states induce the selective weakening of subthreshold synaptic inputs
Slow-wave sleep is thought to be important for retuning cortical synapses, but the cellular mechanisms remain unresolved. During slow-wave activity, cortical neurons display synchronized transitions between depolarized Up states and hyperpolarized Down states. Here, using recordings from LIII pyrami...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610171/ https://www.ncbi.nlm.nih.gov/pubmed/28939859 http://dx.doi.org/10.1038/s41467-017-00748-5 |
_version_ | 1783265724713664512 |
---|---|
author | Bartram, Julian Kahn, Martin C. Tuohy, Simon Paulsen, Ole Wilson, Tony Mann, Edward O. |
author_facet | Bartram, Julian Kahn, Martin C. Tuohy, Simon Paulsen, Ole Wilson, Tony Mann, Edward O. |
author_sort | Bartram, Julian |
collection | PubMed |
description | Slow-wave sleep is thought to be important for retuning cortical synapses, but the cellular mechanisms remain unresolved. During slow-wave activity, cortical neurons display synchronized transitions between depolarized Up states and hyperpolarized Down states. Here, using recordings from LIII pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find that subthreshold inputs arriving during the Up state undergo synaptic weakening. This does not reflect a process of global synaptic downscaling, as it is dependent on presynaptic spiking, with network state encoded in the synaptically evoked spine Ca(2+) responses. Our data indicate that the induction of synaptic weakening is under postsynaptic control, as it can be prevented by correlated postsynaptic spiking activity, and depends on postsynaptic NMDA receptors and GSK3β activity. This provides a mechanism by which slow-wave activity might bias synapses towards weakening, while preserving the synaptic connections within active neuronal assemblies. |
format | Online Article Text |
id | pubmed-5610171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56101712017-09-26 Cortical Up states induce the selective weakening of subthreshold synaptic inputs Bartram, Julian Kahn, Martin C. Tuohy, Simon Paulsen, Ole Wilson, Tony Mann, Edward O. Nat Commun Article Slow-wave sleep is thought to be important for retuning cortical synapses, but the cellular mechanisms remain unresolved. During slow-wave activity, cortical neurons display synchronized transitions between depolarized Up states and hyperpolarized Down states. Here, using recordings from LIII pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find that subthreshold inputs arriving during the Up state undergo synaptic weakening. This does not reflect a process of global synaptic downscaling, as it is dependent on presynaptic spiking, with network state encoded in the synaptically evoked spine Ca(2+) responses. Our data indicate that the induction of synaptic weakening is under postsynaptic control, as it can be prevented by correlated postsynaptic spiking activity, and depends on postsynaptic NMDA receptors and GSK3β activity. This provides a mechanism by which slow-wave activity might bias synapses towards weakening, while preserving the synaptic connections within active neuronal assemblies. Nature Publishing Group UK 2017-09-22 /pmc/articles/PMC5610171/ /pubmed/28939859 http://dx.doi.org/10.1038/s41467-017-00748-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bartram, Julian Kahn, Martin C. Tuohy, Simon Paulsen, Ole Wilson, Tony Mann, Edward O. Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title | Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title_full | Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title_fullStr | Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title_full_unstemmed | Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title_short | Cortical Up states induce the selective weakening of subthreshold synaptic inputs |
title_sort | cortical up states induce the selective weakening of subthreshold synaptic inputs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610171/ https://www.ncbi.nlm.nih.gov/pubmed/28939859 http://dx.doi.org/10.1038/s41467-017-00748-5 |
work_keys_str_mv | AT bartramjulian corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs AT kahnmartinc corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs AT tuohysimon corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs AT paulsenole corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs AT wilsontony corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs AT mannedwardo corticalupstatesinducetheselectiveweakeningofsubthresholdsynapticinputs |