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Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases

Cytoplasmic stress granules (SGs) are critical for facilitating stress responses and for preventing the accumulation of misfolded proteins. SGs, however, have been linked to the pathogenesis of neurodegenerative diseases, in part because SGs share many components with neuronal granules. Oxidative st...

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Detalles Bibliográficos
Autores principales: Chen, Lihua, Liu, Beidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286466/
https://www.ncbi.nlm.nih.gov/pubmed/28194255
http://dx.doi.org/10.1155/2017/1809592
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author Chen, Lihua
Liu, Beidong
author_facet Chen, Lihua
Liu, Beidong
author_sort Chen, Lihua
collection PubMed
description Cytoplasmic stress granules (SGs) are critical for facilitating stress responses and for preventing the accumulation of misfolded proteins. SGs, however, have been linked to the pathogenesis of neurodegenerative diseases, in part because SGs share many components with neuronal granules. Oxidative stress is one of the conditions that induce SG formation. SGs regulate redox levels, and SG formation in turn is differently regulated by various types of oxidative stress. These associations and other evidences suggest that SG formation contributes to the development of neurodegenerative diseases. In this paper, we review the regulation of SG formation/assembly and discuss the interactions between oxidative stress and SG formation. We then discuss the links between SGs and neurodegenerative diseases and the current therapeutic approaches for neurodegenerative diseases that target SGs.
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spelling pubmed-52864662017-02-13 Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases Chen, Lihua Liu, Beidong Oxid Med Cell Longev Review Article Cytoplasmic stress granules (SGs) are critical for facilitating stress responses and for preventing the accumulation of misfolded proteins. SGs, however, have been linked to the pathogenesis of neurodegenerative diseases, in part because SGs share many components with neuronal granules. Oxidative stress is one of the conditions that induce SG formation. SGs regulate redox levels, and SG formation in turn is differently regulated by various types of oxidative stress. These associations and other evidences suggest that SG formation contributes to the development of neurodegenerative diseases. In this paper, we review the regulation of SG formation/assembly and discuss the interactions between oxidative stress and SG formation. We then discuss the links between SGs and neurodegenerative diseases and the current therapeutic approaches for neurodegenerative diseases that target SGs. Hindawi Publishing Corporation 2017 2017-01-18 /pmc/articles/PMC5286466/ /pubmed/28194255 http://dx.doi.org/10.1155/2017/1809592 Text en Copyright © 2017 L. Chen and B. Liu. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Chen, Lihua
Liu, Beidong
Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title_full Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title_fullStr Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title_full_unstemmed Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title_short Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
title_sort relationships between stress granules, oxidative stress, and neurodegenerative diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286466/
https://www.ncbi.nlm.nih.gov/pubmed/28194255
http://dx.doi.org/10.1155/2017/1809592
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