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GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis
GJA1 (connexin43) has been predicted as the top key driver of an astrocyte enriched subnetwork associated with Alzheimer’s disease (AD). In this study, we comprehensively examined GJA1 expression across 29 transcriptomic and proteomic datasets from post-mortem AD and normal control brains. We demons...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303945/ https://www.ncbi.nlm.nih.gov/pubmed/30577786 http://dx.doi.org/10.1186/s40478-018-0642-x |
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author | Kajiwara, Yuji Wang, Erming Wang, Minghui Sin, Wun Chey Brennand, Kristen J. Schadt, Eric Naus, Christian C. Buxbaum, Joseph Zhang, Bin |
author_facet | Kajiwara, Yuji Wang, Erming Wang, Minghui Sin, Wun Chey Brennand, Kristen J. Schadt, Eric Naus, Christian C. Buxbaum, Joseph Zhang, Bin |
author_sort | Kajiwara, Yuji |
collection | PubMed |
description | GJA1 (connexin43) has been predicted as the top key driver of an astrocyte enriched subnetwork associated with Alzheimer’s disease (AD). In this study, we comprehensively examined GJA1 expression across 29 transcriptomic and proteomic datasets from post-mortem AD and normal control brains. We demonstrated that GJA1 was strongly associated with AD amyloid and tau pathologies and cognitive functions. RNA sequencing analysis of Gja1−/− astrocytes validated that Gja1 regulated the subnetwork identified in AD, and many genes involved in Aβ metabolism. Astrocytes lacking Gja1 showed reduced Apoe protein levels as well as impaired Aβ phagocytosis. Consistent with this, wildtype neurons co-cultured with Gja1−/− astrocytes contained higher levels of Aβ species than those with wildtype astrocytes. Moreover, Gja1−/− astrocytes was more neuroprotective under Aβ stress. Our results underscore the importance of GJA1 in AD pathogenesis and its potential for further investigation as a promising pharmacological target in AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-018-0642-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6303945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63039452018-12-31 GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis Kajiwara, Yuji Wang, Erming Wang, Minghui Sin, Wun Chey Brennand, Kristen J. Schadt, Eric Naus, Christian C. Buxbaum, Joseph Zhang, Bin Acta Neuropathol Commun Research GJA1 (connexin43) has been predicted as the top key driver of an astrocyte enriched subnetwork associated with Alzheimer’s disease (AD). In this study, we comprehensively examined GJA1 expression across 29 transcriptomic and proteomic datasets from post-mortem AD and normal control brains. We demonstrated that GJA1 was strongly associated with AD amyloid and tau pathologies and cognitive functions. RNA sequencing analysis of Gja1−/− astrocytes validated that Gja1 regulated the subnetwork identified in AD, and many genes involved in Aβ metabolism. Astrocytes lacking Gja1 showed reduced Apoe protein levels as well as impaired Aβ phagocytosis. Consistent with this, wildtype neurons co-cultured with Gja1−/− astrocytes contained higher levels of Aβ species than those with wildtype astrocytes. Moreover, Gja1−/− astrocytes was more neuroprotective under Aβ stress. Our results underscore the importance of GJA1 in AD pathogenesis and its potential for further investigation as a promising pharmacological target in AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-018-0642-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-21 /pmc/articles/PMC6303945/ /pubmed/30577786 http://dx.doi.org/10.1186/s40478-018-0642-x Text en © The Author(s). 2018 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 Kajiwara, Yuji Wang, Erming Wang, Minghui Sin, Wun Chey Brennand, Kristen J. Schadt, Eric Naus, Christian C. Buxbaum, Joseph Zhang, Bin GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title | GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title_full | GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title_fullStr | GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title_full_unstemmed | GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title_short | GJA1 (connexin43) is a key regulator of Alzheimer’s disease pathogenesis |
title_sort | gja1 (connexin43) is a key regulator of alzheimer’s disease pathogenesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303945/ https://www.ncbi.nlm.nih.gov/pubmed/30577786 http://dx.doi.org/10.1186/s40478-018-0642-x |
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