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Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology

Spinocerebellar ataxias 2 and 3 (SCA2 and SCA3) are dominantly inherited neurodegenerative diseases caused by expansion of polyglutamine-encoding CAG repeats in the affected genes. The etiology of these disorders is known to involve widespread loss of neuronal cells in the cerebellum, however, the m...

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Autores principales: Chuang, Ching-Yu, Yang, Chih-Chao, Soong, Bing-Wen, Yu, Chun-Ying, Chen, Shu-Hwa, Huang, Hsiang-Po, Kuo, Hung-Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361947/
https://www.ncbi.nlm.nih.gov/pubmed/30718627
http://dx.doi.org/10.1038/s41598-018-37774-2
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author Chuang, Ching-Yu
Yang, Chih-Chao
Soong, Bing-Wen
Yu, Chun-Ying
Chen, Shu-Hwa
Huang, Hsiang-Po
Kuo, Hung-Chih
author_facet Chuang, Ching-Yu
Yang, Chih-Chao
Soong, Bing-Wen
Yu, Chun-Ying
Chen, Shu-Hwa
Huang, Hsiang-Po
Kuo, Hung-Chih
author_sort Chuang, Ching-Yu
collection PubMed
description Spinocerebellar ataxias 2 and 3 (SCA2 and SCA3) are dominantly inherited neurodegenerative diseases caused by expansion of polyglutamine-encoding CAG repeats in the affected genes. The etiology of these disorders is known to involve widespread loss of neuronal cells in the cerebellum, however, the mechanisms that contribute to cell death are still elusive. Here we established SCA2 and SCA3 induced pluripotent stem cells (iPSCs) and demonstrated that SCA-associated pathological features can be recapitulated in SCA-iPSC-derived neurons. Importantly, our results also revealed that glutamate stimulation promotes the development of disease-related phenotypes in SCA-iPSC-derived neurons, including altered composition of glutamatergic receptors, destabilized intracellular calcium, and eventual cell death. Furthermore, anti-glutamate drugs and calcium stabilizer treatment protected the SCA-iPSC-derived neurons and reduced cell death. Collectively, our study demonstrates that the SCA-iPSC-derived neurons can recapitulate SCA-associated pathological features, providing a valuable tool to explore SCA pathogenic mechanisms and screen drugs to identify potential SCA therapeutics.
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spelling pubmed-63619472019-02-06 Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology Chuang, Ching-Yu Yang, Chih-Chao Soong, Bing-Wen Yu, Chun-Ying Chen, Shu-Hwa Huang, Hsiang-Po Kuo, Hung-Chih Sci Rep Article Spinocerebellar ataxias 2 and 3 (SCA2 and SCA3) are dominantly inherited neurodegenerative diseases caused by expansion of polyglutamine-encoding CAG repeats in the affected genes. The etiology of these disorders is known to involve widespread loss of neuronal cells in the cerebellum, however, the mechanisms that contribute to cell death are still elusive. Here we established SCA2 and SCA3 induced pluripotent stem cells (iPSCs) and demonstrated that SCA-associated pathological features can be recapitulated in SCA-iPSC-derived neurons. Importantly, our results also revealed that glutamate stimulation promotes the development of disease-related phenotypes in SCA-iPSC-derived neurons, including altered composition of glutamatergic receptors, destabilized intracellular calcium, and eventual cell death. Furthermore, anti-glutamate drugs and calcium stabilizer treatment protected the SCA-iPSC-derived neurons and reduced cell death. Collectively, our study demonstrates that the SCA-iPSC-derived neurons can recapitulate SCA-associated pathological features, providing a valuable tool to explore SCA pathogenic mechanisms and screen drugs to identify potential SCA therapeutics. Nature Publishing Group UK 2019-02-04 /pmc/articles/PMC6361947/ /pubmed/30718627 http://dx.doi.org/10.1038/s41598-018-37774-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chuang, Ching-Yu
Yang, Chih-Chao
Soong, Bing-Wen
Yu, Chun-Ying
Chen, Shu-Hwa
Huang, Hsiang-Po
Kuo, Hung-Chih
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title_full Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title_fullStr Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title_full_unstemmed Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title_short Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathology
title_sort modeling spinocerebellar ataxias 2 and 3 with ipscs reveals a role for glutamate in disease pathology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361947/
https://www.ncbi.nlm.nih.gov/pubmed/30718627
http://dx.doi.org/10.1038/s41598-018-37774-2
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