Cargando…
Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1
Brief periods of sleep loss have long-lasting consequences such as impaired memory consolidation. Structural changes in synaptic connectivity have been proposed as a substrate of memory storage. Here, we examine the impact of brief periods of sleep deprivation on dendritic structure. In mice, we fin...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996653/ https://www.ncbi.nlm.nih.gov/pubmed/27549340 http://dx.doi.org/10.7554/eLife.13424 |
_version_ | 1782449643347509248 |
---|---|
author | Havekes, Robbert Park, Alan J Tudor, Jennifer C Luczak, Vincent G Hansen, Rolf T Ferri, Sarah L Bruinenberg, Vibeke M Poplawski, Shane G Day, Jonathan P Aton, Sara J Radwańska, Kasia Meerlo, Peter Houslay, Miles D Baillie, George S Abel, Ted |
author_facet | Havekes, Robbert Park, Alan J Tudor, Jennifer C Luczak, Vincent G Hansen, Rolf T Ferri, Sarah L Bruinenberg, Vibeke M Poplawski, Shane G Day, Jonathan P Aton, Sara J Radwańska, Kasia Meerlo, Peter Houslay, Miles D Baillie, George S Abel, Ted |
author_sort | Havekes, Robbert |
collection | PubMed |
description | Brief periods of sleep loss have long-lasting consequences such as impaired memory consolidation. Structural changes in synaptic connectivity have been proposed as a substrate of memory storage. Here, we examine the impact of brief periods of sleep deprivation on dendritic structure. In mice, we find that five hours of sleep deprivation decreases dendritic spine numbers selectively in hippocampal area CA1 and increased activity of the filamentous actin severing protein cofilin. Recovery sleep normalizes these structural alterations. Suppression of cofilin function prevents spine loss, deficits in hippocampal synaptic plasticity, and impairments in long-term memory caused by sleep deprivation. The elevated cofilin activity is caused by cAMP-degrading phosphodiesterase-4A5 (PDE4A5), which hampers cAMP-PKA-LIMK signaling. Attenuating PDE4A5 function prevents changes in cAMP-PKA-LIMK-cofilin signaling and cognitive deficits associated with sleep deprivation. Our work demonstrates the necessity of an intact cAMP-PDE4-PKA-LIMK-cofilin activation-signaling pathway for sleep deprivation-induced memory disruption and reduction in hippocampal spine density. DOI: http://dx.doi.org/10.7554/eLife.13424.001 |
format | Online Article Text |
id | pubmed-4996653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49966532016-08-29 Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 Havekes, Robbert Park, Alan J Tudor, Jennifer C Luczak, Vincent G Hansen, Rolf T Ferri, Sarah L Bruinenberg, Vibeke M Poplawski, Shane G Day, Jonathan P Aton, Sara J Radwańska, Kasia Meerlo, Peter Houslay, Miles D Baillie, George S Abel, Ted eLife Neuroscience Brief periods of sleep loss have long-lasting consequences such as impaired memory consolidation. Structural changes in synaptic connectivity have been proposed as a substrate of memory storage. Here, we examine the impact of brief periods of sleep deprivation on dendritic structure. In mice, we find that five hours of sleep deprivation decreases dendritic spine numbers selectively in hippocampal area CA1 and increased activity of the filamentous actin severing protein cofilin. Recovery sleep normalizes these structural alterations. Suppression of cofilin function prevents spine loss, deficits in hippocampal synaptic plasticity, and impairments in long-term memory caused by sleep deprivation. The elevated cofilin activity is caused by cAMP-degrading phosphodiesterase-4A5 (PDE4A5), which hampers cAMP-PKA-LIMK signaling. Attenuating PDE4A5 function prevents changes in cAMP-PKA-LIMK-cofilin signaling and cognitive deficits associated with sleep deprivation. Our work demonstrates the necessity of an intact cAMP-PDE4-PKA-LIMK-cofilin activation-signaling pathway for sleep deprivation-induced memory disruption and reduction in hippocampal spine density. DOI: http://dx.doi.org/10.7554/eLife.13424.001 eLife Sciences Publications, Ltd 2016-08-23 /pmc/articles/PMC4996653/ /pubmed/27549340 http://dx.doi.org/10.7554/eLife.13424 Text en © 2016, Havekes et al 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 Havekes, Robbert Park, Alan J Tudor, Jennifer C Luczak, Vincent G Hansen, Rolf T Ferri, Sarah L Bruinenberg, Vibeke M Poplawski, Shane G Day, Jonathan P Aton, Sara J Radwańska, Kasia Meerlo, Peter Houslay, Miles D Baillie, George S Abel, Ted Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title | Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title_full | Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title_fullStr | Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title_full_unstemmed | Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title_short | Sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area CA1 |
title_sort | sleep deprivation causes memory deficits by negatively impacting neuronal connectivity in hippocampal area ca1 |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996653/ https://www.ncbi.nlm.nih.gov/pubmed/27549340 http://dx.doi.org/10.7554/eLife.13424 |
work_keys_str_mv | AT havekesrobbert sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT parkalanj sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT tudorjenniferc sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT luczakvincentg sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT hansenrolft sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT ferrisarahl sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT bruinenbergvibekem sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT poplawskishaneg sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT dayjonathanp sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT atonsaraj sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT radwanskakasia sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT meerlopeter sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT houslaymilesd sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT bailliegeorges sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 AT abelted sleepdeprivationcausesmemorydeficitsbynegativelyimpactingneuronalconnectivityinhippocampalareaca1 |