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SIRT1 and SIRT2: emerging targets in neurodegeneration

Sirtuins are NAD-dependent protein deacetylases known to have protective effects against age-related diseases such as cancer, diabetes, cardiovascular and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversity in subcellular localization and function. Whi...

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Detalles Bibliográficos
Autores principales: Donmez, Gizem, Outeiro, Tiago F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598076/
https://www.ncbi.nlm.nih.gov/pubmed/23417962
http://dx.doi.org/10.1002/emmm.201302451
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author Donmez, Gizem
Outeiro, Tiago F
author_facet Donmez, Gizem
Outeiro, Tiago F
author_sort Donmez, Gizem
collection PubMed
description Sirtuins are NAD-dependent protein deacetylases known to have protective effects against age-related diseases such as cancer, diabetes, cardiovascular and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversity in subcellular localization and function. While SIRT1 has been extensively investigated due to its initial connection with lifespan extension and involvement in calorie restriction, important biological and therapeutic roles of other sirtuins have only recently been recognized. Here, we review the potential roles and effects of SIRT1 and SIRT2 in neurodegenerative diseases. We discuss different functions and targets of SIRT1 and SIRT2 in a variety of neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD) and Huntington's Disease (HD). We also cover the role of SIRT1 in neuronal differentiation due to the possible implications in neurodegenerative conditions, and conclude with an outlook on the potential therapeutic value of SIRT1 and SIRT2 in these disorders.
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spelling pubmed-35980762013-03-19 SIRT1 and SIRT2: emerging targets in neurodegeneration Donmez, Gizem Outeiro, Tiago F EMBO Mol Med Reviews Sirtuins are NAD-dependent protein deacetylases known to have protective effects against age-related diseases such as cancer, diabetes, cardiovascular and neurodegenerative diseases. In mammals, there are seven sirtuins (SIRT1-7), which display diversity in subcellular localization and function. While SIRT1 has been extensively investigated due to its initial connection with lifespan extension and involvement in calorie restriction, important biological and therapeutic roles of other sirtuins have only recently been recognized. Here, we review the potential roles and effects of SIRT1 and SIRT2 in neurodegenerative diseases. We discuss different functions and targets of SIRT1 and SIRT2 in a variety of neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD) and Huntington's Disease (HD). We also cover the role of SIRT1 in neuronal differentiation due to the possible implications in neurodegenerative conditions, and conclude with an outlook on the potential therapeutic value of SIRT1 and SIRT2 in these disorders. WILEY-VCH Verlag 2013-03 2013-02-18 /pmc/articles/PMC3598076/ /pubmed/23417962 http://dx.doi.org/10.1002/emmm.201302451 Text en Copyright © 2013 The Authors. Published by John Wiley and Sons, Ltd on behalf of EMBO http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Reviews
Donmez, Gizem
Outeiro, Tiago F
SIRT1 and SIRT2: emerging targets in neurodegeneration
title SIRT1 and SIRT2: emerging targets in neurodegeneration
title_full SIRT1 and SIRT2: emerging targets in neurodegeneration
title_fullStr SIRT1 and SIRT2: emerging targets in neurodegeneration
title_full_unstemmed SIRT1 and SIRT2: emerging targets in neurodegeneration
title_short SIRT1 and SIRT2: emerging targets in neurodegeneration
title_sort sirt1 and sirt2: emerging targets in neurodegeneration
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598076/
https://www.ncbi.nlm.nih.gov/pubmed/23417962
http://dx.doi.org/10.1002/emmm.201302451
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