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Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function
In bilaterian central nervous systems, coordination of neurotransmission by glial cells enables highly sophisticated neural functions. The diversity of transcription factors (TFs) involved in gliogenesis suggests multiple evolutionary origins of various glial cell types of bilaterians. Many of these...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491807/ https://www.ncbi.nlm.nih.gov/pubmed/37684386 http://dx.doi.org/10.1038/s41598-023-42046-9 |
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author | Sheloukhova, Larisa Watanabe, Hiroshi |
author_facet | Sheloukhova, Larisa Watanabe, Hiroshi |
author_sort | Sheloukhova, Larisa |
collection | PubMed |
description | In bilaterian central nervous systems, coordination of neurotransmission by glial cells enables highly sophisticated neural functions. The diversity of transcription factors (TFs) involved in gliogenesis suggests multiple evolutionary origins of various glial cell types of bilaterians. Many of these TFs including the glial cells missing (Gcm) are also present in genomes of Cnidaria, the closest outgroup to Bilateria, but their function remains to be elucidated. In this study, we analyzed the function of Gcm, a multifunctional TF involved in development of glial and non-glial cell types, in the sea anemone, Nematostella vectensis. siRNA-mediated knockdown of Nematostella Gcm altered expression of cell adhesion proteins, glutamate and GABA transporters, ion channels, metabolic enzymes, and zinc finger and Ets-related TFs. NvGcm and mRNAs of downstream genes are expressed in broad neural cell clusters. However, immunostaining of a NvGcm target protein, the glutamate transporter, NvEAAT1, visualized a novel class of cells with flat cell bodies and no clear processes. Together with the finding of unique morphological features of NvEAAT1-functioning cells, these data suggest that extracellular glutamate metabolism, one of major glial functions, is deployed downstream of Gcm in specific neural cell types in Cnidaria. |
format | Online Article Text |
id | pubmed-10491807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104918072023-09-10 Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function Sheloukhova, Larisa Watanabe, Hiroshi Sci Rep Article In bilaterian central nervous systems, coordination of neurotransmission by glial cells enables highly sophisticated neural functions. The diversity of transcription factors (TFs) involved in gliogenesis suggests multiple evolutionary origins of various glial cell types of bilaterians. Many of these TFs including the glial cells missing (Gcm) are also present in genomes of Cnidaria, the closest outgroup to Bilateria, but their function remains to be elucidated. In this study, we analyzed the function of Gcm, a multifunctional TF involved in development of glial and non-glial cell types, in the sea anemone, Nematostella vectensis. siRNA-mediated knockdown of Nematostella Gcm altered expression of cell adhesion proteins, glutamate and GABA transporters, ion channels, metabolic enzymes, and zinc finger and Ets-related TFs. NvGcm and mRNAs of downstream genes are expressed in broad neural cell clusters. However, immunostaining of a NvGcm target protein, the glutamate transporter, NvEAAT1, visualized a novel class of cells with flat cell bodies and no clear processes. Together with the finding of unique morphological features of NvEAAT1-functioning cells, these data suggest that extracellular glutamate metabolism, one of major glial functions, is deployed downstream of Gcm in specific neural cell types in Cnidaria. Nature Publishing Group UK 2023-09-08 /pmc/articles/PMC10491807/ /pubmed/37684386 http://dx.doi.org/10.1038/s41598-023-42046-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sheloukhova, Larisa Watanabe, Hiroshi Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title | Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title_full | Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title_fullStr | Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title_full_unstemmed | Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title_short | Analysis of cnidarian Gcm suggests a neuronal origin of glial EAAT1 function |
title_sort | analysis of cnidarian gcm suggests a neuronal origin of glial eaat1 function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491807/ https://www.ncbi.nlm.nih.gov/pubmed/37684386 http://dx.doi.org/10.1038/s41598-023-42046-9 |
work_keys_str_mv | AT sheloukhovalarisa analysisofcnidariangcmsuggestsaneuronaloriginofglialeaat1function AT watanabehiroshi analysisofcnidariangcmsuggestsaneuronaloriginofglialeaat1function |