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Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases

Protein homeostasis or proteostasis is a fundamental cellular property that encompasses the dynamic balancing of processes in the proteostasis network (PN). Such processes include protein synthesis, folding, and degradation in both non-stressed and stressful conditions. The role of the PN in neurode...

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Detalles Bibliográficos
Autores principales: Bhore, Noopur, Wang, Bo-Jeng, Chen, Yun-Wen, Liao, Yung-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618612/
https://www.ncbi.nlm.nih.gov/pubmed/28902166
http://dx.doi.org/10.3390/ijms18091963
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author Bhore, Noopur
Wang, Bo-Jeng
Chen, Yun-Wen
Liao, Yung-Feng
author_facet Bhore, Noopur
Wang, Bo-Jeng
Chen, Yun-Wen
Liao, Yung-Feng
author_sort Bhore, Noopur
collection PubMed
description Protein homeostasis or proteostasis is a fundamental cellular property that encompasses the dynamic balancing of processes in the proteostasis network (PN). Such processes include protein synthesis, folding, and degradation in both non-stressed and stressful conditions. The role of the PN in neurodegenerative disease is well-documented, where it is known to respond to changes in protein folding states or toxic gain-of-function protein aggregation. Dual-specificity phosphatases have recently emerged as important participants in maintaining balance within the PN, acting through modulation of cellular signaling pathways that are involved in neurodegeneration. In this review, we will summarize recent findings describing the roles of dual-specificity phosphatases in neurodegeneration and offer perspectives on future therapeutic directions.
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spelling pubmed-56186122017-09-30 Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases Bhore, Noopur Wang, Bo-Jeng Chen, Yun-Wen Liao, Yung-Feng Int J Mol Sci Review Protein homeostasis or proteostasis is a fundamental cellular property that encompasses the dynamic balancing of processes in the proteostasis network (PN). Such processes include protein synthesis, folding, and degradation in both non-stressed and stressful conditions. The role of the PN in neurodegenerative disease is well-documented, where it is known to respond to changes in protein folding states or toxic gain-of-function protein aggregation. Dual-specificity phosphatases have recently emerged as important participants in maintaining balance within the PN, acting through modulation of cellular signaling pathways that are involved in neurodegeneration. In this review, we will summarize recent findings describing the roles of dual-specificity phosphatases in neurodegeneration and offer perspectives on future therapeutic directions. MDPI 2017-09-13 /pmc/articles/PMC5618612/ /pubmed/28902166 http://dx.doi.org/10.3390/ijms18091963 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bhore, Noopur
Wang, Bo-Jeng
Chen, Yun-Wen
Liao, Yung-Feng
Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title_full Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title_fullStr Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title_full_unstemmed Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title_short Critical Roles of Dual-Specificity Phosphatases in Neuronal Proteostasis and Neurological Diseases
title_sort critical roles of dual-specificity phosphatases in neuronal proteostasis and neurological diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618612/
https://www.ncbi.nlm.nih.gov/pubmed/28902166
http://dx.doi.org/10.3390/ijms18091963
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