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Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease

Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by expansion of the polyglutamine domain of the ataxin-3 (ATX3) protein. MJD/SCA3 is the most frequent autosomal dominant ataxia in many countries. The mechanism underlying...

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Autores principales: Lopes-Ramos, C.M., Pereira, T.C., Dogini, D.B., Gilioli, R., Lopes-Cendes, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5188859/
https://www.ncbi.nlm.nih.gov/pubmed/27878228
http://dx.doi.org/10.1590/1414-431X20165805
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author Lopes-Ramos, C.M.
Pereira, T.C.
Dogini, D.B.
Gilioli, R.
Lopes-Cendes, I.
author_facet Lopes-Ramos, C.M.
Pereira, T.C.
Dogini, D.B.
Gilioli, R.
Lopes-Cendes, I.
author_sort Lopes-Ramos, C.M.
collection PubMed
description Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by expansion of the polyglutamine domain of the ataxin-3 (ATX3) protein. MJD/SCA3 is the most frequent autosomal dominant ataxia in many countries. The mechanism underlying MJD/SCA3 is thought to be mainly related to protein misfolding and aggregation leading to neuronal dysfunction followed by cell death. Currently, there are no effective treatments for patients with MJD/SCA3. Here, we report on the potential use of lithium carbonate and coenzyme Q10 to reduce cell death caused by the expanded ATX3 in cell culture. Cell viability and apoptosis were evaluated by MTT assay and by flow cytometry after staining with annexin V-FITC/propidium iodide. Treatment with lithium carbonate and coenzyme Q10 led to a significant increase in viability of cells expressing expanded ATX3 (Q84). In addition, we found that the increase in cell viability resulted from a significant reduction in the proportion of apoptotic cells. Furthermore, there was a significant change in the expanded ATX3 monomer/aggregate ratio after lithium carbonate and coenzyme Q10 treatment, with an increase in the monomer fraction and decrease in aggregates. The safety and tolerance of both drugs are well established; thus, our results indicate that lithium carbonate and coenzyme Q10 are good candidates for further in vivo therapeutic trials.
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spelling pubmed-51888592017-01-11 Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease Lopes-Ramos, C.M. Pereira, T.C. Dogini, D.B. Gilioli, R. Lopes-Cendes, I. Braz J Med Biol Res Biomedical Sciences Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by expansion of the polyglutamine domain of the ataxin-3 (ATX3) protein. MJD/SCA3 is the most frequent autosomal dominant ataxia in many countries. The mechanism underlying MJD/SCA3 is thought to be mainly related to protein misfolding and aggregation leading to neuronal dysfunction followed by cell death. Currently, there are no effective treatments for patients with MJD/SCA3. Here, we report on the potential use of lithium carbonate and coenzyme Q10 to reduce cell death caused by the expanded ATX3 in cell culture. Cell viability and apoptosis were evaluated by MTT assay and by flow cytometry after staining with annexin V-FITC/propidium iodide. Treatment with lithium carbonate and coenzyme Q10 led to a significant increase in viability of cells expressing expanded ATX3 (Q84). In addition, we found that the increase in cell viability resulted from a significant reduction in the proportion of apoptotic cells. Furthermore, there was a significant change in the expanded ATX3 monomer/aggregate ratio after lithium carbonate and coenzyme Q10 treatment, with an increase in the monomer fraction and decrease in aggregates. The safety and tolerance of both drugs are well established; thus, our results indicate that lithium carbonate and coenzyme Q10 are good candidates for further in vivo therapeutic trials. Associação Brasileira de Divulgação Científica 2016-11-21 /pmc/articles/PMC5188859/ /pubmed/27878228 http://dx.doi.org/10.1590/1414-431X20165805 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biomedical Sciences
Lopes-Ramos, C.M.
Pereira, T.C.
Dogini, D.B.
Gilioli, R.
Lopes-Cendes, I.
Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title_full Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title_fullStr Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title_full_unstemmed Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title_short Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
title_sort lithium carbonate and coenzyme q10 reduce cell death in a cell model of machado-joseph disease
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5188859/
https://www.ncbi.nlm.nih.gov/pubmed/27878228
http://dx.doi.org/10.1590/1414-431X20165805
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