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Valproic acid-exposed astrocytes impair inhibitory synapse formation and function
Valproic acid (VPA) is widely prescribed to treat epilepsy. Maternal VPA use is, however, clinically restricted because of the severe risk that VPA may cause neurodevelopmental disorders in offspring, such as autism spectrum disorder. Understanding the negative action of VPA may help to prevent VPA-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794250/ https://www.ncbi.nlm.nih.gov/pubmed/33420078 http://dx.doi.org/10.1038/s41598-020-79520-7 |
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author | Takeda, Kotomi Watanabe, Takuya Oyabu, Kohei Tsukamoto, Shuntaro Oba, Yuki Nakano, Takafumi Kubota, Kaori Katsurabayashi, Shutaro Iwasaki, Katsunori |
author_facet | Takeda, Kotomi Watanabe, Takuya Oyabu, Kohei Tsukamoto, Shuntaro Oba, Yuki Nakano, Takafumi Kubota, Kaori Katsurabayashi, Shutaro Iwasaki, Katsunori |
author_sort | Takeda, Kotomi |
collection | PubMed |
description | Valproic acid (VPA) is widely prescribed to treat epilepsy. Maternal VPA use is, however, clinically restricted because of the severe risk that VPA may cause neurodevelopmental disorders in offspring, such as autism spectrum disorder. Understanding the negative action of VPA may help to prevent VPA-induced neurodevelopmental disorders. Astrocytes play a vital role in neurodevelopment and synapse function; however, the impact of VPA on astrocyte involvement in neurodevelopment and synapse function has not been examined. In this study, we examined whether exposure of cultured astrocytes to VPA alters neuronal morphology and synapse function of co-cultured neurons. We show that synaptic transmission by inhibitory neurons was small because VPA-exposed astrocytes reduced the number of inhibitory synapses. However, synaptic transmission by excitatory neurons and the number of excitatory synapses were normal with VPA-exposed astrocytes. VPA-exposed astrocytes did not affect the morphology of inhibitory neurons. These data indicate that VPA-exposed astrocytes impair synaptogenesis specifically of inhibitory neurons. Our results indicate that maternal use of VPA would affect not only neurons but also astrocytes and would result in perturbed astrocyte-mediated neurodevelopment. |
format | Online Article Text |
id | pubmed-7794250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77942502021-01-11 Valproic acid-exposed astrocytes impair inhibitory synapse formation and function Takeda, Kotomi Watanabe, Takuya Oyabu, Kohei Tsukamoto, Shuntaro Oba, Yuki Nakano, Takafumi Kubota, Kaori Katsurabayashi, Shutaro Iwasaki, Katsunori Sci Rep Article Valproic acid (VPA) is widely prescribed to treat epilepsy. Maternal VPA use is, however, clinically restricted because of the severe risk that VPA may cause neurodevelopmental disorders in offspring, such as autism spectrum disorder. Understanding the negative action of VPA may help to prevent VPA-induced neurodevelopmental disorders. Astrocytes play a vital role in neurodevelopment and synapse function; however, the impact of VPA on astrocyte involvement in neurodevelopment and synapse function has not been examined. In this study, we examined whether exposure of cultured astrocytes to VPA alters neuronal morphology and synapse function of co-cultured neurons. We show that synaptic transmission by inhibitory neurons was small because VPA-exposed astrocytes reduced the number of inhibitory synapses. However, synaptic transmission by excitatory neurons and the number of excitatory synapses were normal with VPA-exposed astrocytes. VPA-exposed astrocytes did not affect the morphology of inhibitory neurons. These data indicate that VPA-exposed astrocytes impair synaptogenesis specifically of inhibitory neurons. Our results indicate that maternal use of VPA would affect not only neurons but also astrocytes and would result in perturbed astrocyte-mediated neurodevelopment. Nature Publishing Group UK 2021-01-08 /pmc/articles/PMC7794250/ /pubmed/33420078 http://dx.doi.org/10.1038/s41598-020-79520-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Takeda, Kotomi Watanabe, Takuya Oyabu, Kohei Tsukamoto, Shuntaro Oba, Yuki Nakano, Takafumi Kubota, Kaori Katsurabayashi, Shutaro Iwasaki, Katsunori Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title | Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title_full | Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title_fullStr | Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title_full_unstemmed | Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title_short | Valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
title_sort | valproic acid-exposed astrocytes impair inhibitory synapse formation and function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794250/ https://www.ncbi.nlm.nih.gov/pubmed/33420078 http://dx.doi.org/10.1038/s41598-020-79520-7 |
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