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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...

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Autores principales: 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
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
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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
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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
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