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Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons

Sleep deprivation has a negative impact on hippocampus‐dependent memory, which is thought to depend on cellular plasticity. We previously found that 5 h of sleep deprivation robustly decreases dendritic spine density in the CA1 area of the hippocampus in adult male mice. However, recent work by othe...

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Autores principales: Bolsius, Youri G., Meerlo, Peter, Kas, Martien J., Abel, Ted, Havekes, Robbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760357/
https://www.ncbi.nlm.nih.gov/pubmed/34263991
http://dx.doi.org/10.1111/jsr.13438
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author Bolsius, Youri G.
Meerlo, Peter
Kas, Martien J.
Abel, Ted
Havekes, Robbert
author_facet Bolsius, Youri G.
Meerlo, Peter
Kas, Martien J.
Abel, Ted
Havekes, Robbert
author_sort Bolsius, Youri G.
collection PubMed
description Sleep deprivation has a negative impact on hippocampus‐dependent memory, which is thought to depend on cellular plasticity. We previously found that 5 h of sleep deprivation robustly decreases dendritic spine density in the CA1 area of the hippocampus in adult male mice. However, recent work by others suggests that sleep deprivation increases the density of certain spine types on specific dendritic branches. Based on these recent findings and our previous work, we conducted a more in‐depth analysis of different spine types on branches 1, 2 and 5 of both apical and basal dendrites to assess whether 5 h of sleep deprivation may have previously unrecognized spine‐type and branch‐specific effects. This analysis shows no spine‐type specific changes on branch 1 and 2 of apical dendrites after sleep deprivation. In contrast, sleep deprivation decreases the number of mushroom and branched spines on branch 5. Likewise, sleep deprivation reduces thin, mushroom and filopodia spine density on branch 5 of the basal dendrites, without affecting spines on branch 1 and 2. Our findings indicate that sleep deprivation leads to local branch‐specific reduction in the density of individual spine types, and that local effects might not reflect the overall impact of sleep deprivation on CA1 structural plasticity. Moreover, our analysis underscores that focusing on a subset of dendritic branches may lead to potential misinterpretation of the overall impact of, in this case, sleep deprivation on structural plasticity.
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spelling pubmed-87603572022-10-14 Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons Bolsius, Youri G. Meerlo, Peter Kas, Martien J. Abel, Ted Havekes, Robbert J Sleep Res Sleep Deprivation Sleep deprivation has a negative impact on hippocampus‐dependent memory, which is thought to depend on cellular plasticity. We previously found that 5 h of sleep deprivation robustly decreases dendritic spine density in the CA1 area of the hippocampus in adult male mice. However, recent work by others suggests that sleep deprivation increases the density of certain spine types on specific dendritic branches. Based on these recent findings and our previous work, we conducted a more in‐depth analysis of different spine types on branches 1, 2 and 5 of both apical and basal dendrites to assess whether 5 h of sleep deprivation may have previously unrecognized spine‐type and branch‐specific effects. This analysis shows no spine‐type specific changes on branch 1 and 2 of apical dendrites after sleep deprivation. In contrast, sleep deprivation decreases the number of mushroom and branched spines on branch 5. Likewise, sleep deprivation reduces thin, mushroom and filopodia spine density on branch 5 of the basal dendrites, without affecting spines on branch 1 and 2. Our findings indicate that sleep deprivation leads to local branch‐specific reduction in the density of individual spine types, and that local effects might not reflect the overall impact of sleep deprivation on CA1 structural plasticity. Moreover, our analysis underscores that focusing on a subset of dendritic branches may lead to potential misinterpretation of the overall impact of, in this case, sleep deprivation on structural plasticity. John Wiley and Sons Inc. 2021-07-15 2022-02 /pmc/articles/PMC8760357/ /pubmed/34263991 http://dx.doi.org/10.1111/jsr.13438 Text en © 2021 The Authors. Journal of Sleep Research published by John Wiley & Sons Ltd on behalf of European Sleep Research Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Sleep Deprivation
Bolsius, Youri G.
Meerlo, Peter
Kas, Martien J.
Abel, Ted
Havekes, Robbert
Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title_full Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title_fullStr Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title_full_unstemmed Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title_short Sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in CA1 neurons
title_sort sleep deprivation reduces the density of individual spine subtypes in a branch‐specific fashion in ca1 neurons
topic Sleep Deprivation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760357/
https://www.ncbi.nlm.nih.gov/pubmed/34263991
http://dx.doi.org/10.1111/jsr.13438
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