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Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus

Astrocytes have been reported to exist in two states, the resting and the reactive states. Morphological changes in the reactive state of astrocytes include an increase in thickness and number of processes, and an increase in the size of the cell body. Molecular changes also occur, such as an increa...

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Autores principales: Choi, Moonseok, Ahn, Sangzin, Yang, Eun-Jeong, Kim, Hyunju, Chong, Young Hae, Kim, Hye-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962445/
https://www.ncbi.nlm.nih.gov/pubmed/27460927
http://dx.doi.org/10.1186/s13041-016-0253-z
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author Choi, Moonseok
Ahn, Sangzin
Yang, Eun-Jeong
Kim, Hyunju
Chong, Young Hae
Kim, Hye-Sun
author_facet Choi, Moonseok
Ahn, Sangzin
Yang, Eun-Jeong
Kim, Hyunju
Chong, Young Hae
Kim, Hye-Sun
author_sort Choi, Moonseok
collection PubMed
description Astrocytes have been reported to exist in two states, the resting and the reactive states. Morphological changes in the reactive state of astrocytes include an increase in thickness and number of processes, and an increase in the size of the cell body. Molecular changes also occur, such as an increase in the expression of glial fibrillary acidic protein (GFAP). However, the morphological and molecular changes during the process of learning and memory have not been elucidated. In the current study, we subjected Fvb/n mice to contextual fear conditioning, and checked for morphological and molecular changes in astrocytes. 1 h after fear conditioning, type II and type III astrocytes exhibited a unique status with an increased number of processes and decreased GFAP expression which differed from the typical resting or reactive state. In addition, the protein level of excitatory excitatory amino acid transporter 2 (EAAT2) was increased 1 h to 24 h after contextual fear conditioning while EAAT1 did not show any alterations. Connexin 43 (Cx43) protein was found to be increased at 24 h after fear conditioning. These data suggest that hippocampus-based contextual memory process induces changes in the status of astrocytes towards a novel status different from typical resting or reactive states. These morphological and molecular changes may be in line with functional changes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13041-016-0253-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-49624452016-07-28 Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus Choi, Moonseok Ahn, Sangzin Yang, Eun-Jeong Kim, Hyunju Chong, Young Hae Kim, Hye-Sun Mol Brain Research Astrocytes have been reported to exist in two states, the resting and the reactive states. Morphological changes in the reactive state of astrocytes include an increase in thickness and number of processes, and an increase in the size of the cell body. Molecular changes also occur, such as an increase in the expression of glial fibrillary acidic protein (GFAP). However, the morphological and molecular changes during the process of learning and memory have not been elucidated. In the current study, we subjected Fvb/n mice to contextual fear conditioning, and checked for morphological and molecular changes in astrocytes. 1 h after fear conditioning, type II and type III astrocytes exhibited a unique status with an increased number of processes and decreased GFAP expression which differed from the typical resting or reactive state. In addition, the protein level of excitatory excitatory amino acid transporter 2 (EAAT2) was increased 1 h to 24 h after contextual fear conditioning while EAAT1 did not show any alterations. Connexin 43 (Cx43) protein was found to be increased at 24 h after fear conditioning. These data suggest that hippocampus-based contextual memory process induces changes in the status of astrocytes towards a novel status different from typical resting or reactive states. These morphological and molecular changes may be in line with functional changes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13041-016-0253-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-26 /pmc/articles/PMC4962445/ /pubmed/27460927 http://dx.doi.org/10.1186/s13041-016-0253-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Choi, Moonseok
Ahn, Sangzin
Yang, Eun-Jeong
Kim, Hyunju
Chong, Young Hae
Kim, Hye-Sun
Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title_full Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title_fullStr Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title_full_unstemmed Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title_short Hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
title_sort hippocampus-based contextual memory alters the morphological characteristics of astrocytes in the dentate gyrus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962445/
https://www.ncbi.nlm.nih.gov/pubmed/27460927
http://dx.doi.org/10.1186/s13041-016-0253-z
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