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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8760357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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