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Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases

The ubiquitin-proteasome system (UPS) is one of the major protein degradation pathways, where abnormal UPS function has been observed in cancer and neurological diseases. Many neurodegenerative diseases share a common pathological feature, namely intracellular ubiquitin-positive inclusions formed by...

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Autores principales: Zheng, Qiuyang, Huang, Timothy, Zhang, Lishan, Zhou, Ying, Luo, Hong, Xu, Huaxi, Wang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5156861/
https://www.ncbi.nlm.nih.gov/pubmed/28018215
http://dx.doi.org/10.3389/fnagi.2016.00303
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author Zheng, Qiuyang
Huang, Timothy
Zhang, Lishan
Zhou, Ying
Luo, Hong
Xu, Huaxi
Wang, Xin
author_facet Zheng, Qiuyang
Huang, Timothy
Zhang, Lishan
Zhou, Ying
Luo, Hong
Xu, Huaxi
Wang, Xin
author_sort Zheng, Qiuyang
collection PubMed
description The ubiquitin-proteasome system (UPS) is one of the major protein degradation pathways, where abnormal UPS function has been observed in cancer and neurological diseases. Many neurodegenerative diseases share a common pathological feature, namely intracellular ubiquitin-positive inclusions formed by aggregate-prone neurotoxic proteins. This suggests that dysfunction of the UPS in neurodegenerative diseases contributes to the accumulation of neurotoxic proteins and to instigate neurodegeneration. Here, we review recent findings describing various aspects of UPS dysregulation in neurodegenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and Huntington’s disease.
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spelling pubmed-51568612016-12-23 Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases Zheng, Qiuyang Huang, Timothy Zhang, Lishan Zhou, Ying Luo, Hong Xu, Huaxi Wang, Xin Front Aging Neurosci Neuroscience The ubiquitin-proteasome system (UPS) is one of the major protein degradation pathways, where abnormal UPS function has been observed in cancer and neurological diseases. Many neurodegenerative diseases share a common pathological feature, namely intracellular ubiquitin-positive inclusions formed by aggregate-prone neurotoxic proteins. This suggests that dysfunction of the UPS in neurodegenerative diseases contributes to the accumulation of neurotoxic proteins and to instigate neurodegeneration. Here, we review recent findings describing various aspects of UPS dysregulation in neurodegenerative disorders such as Alzheimer’s disease, Parkinson’s disease, and Huntington’s disease. Frontiers Media S.A. 2016-12-15 /pmc/articles/PMC5156861/ /pubmed/28018215 http://dx.doi.org/10.3389/fnagi.2016.00303 Text en Copyright © 2016 Zheng, Huang, Zhang, Zhou, Luo, Xu and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Zheng, Qiuyang
Huang, Timothy
Zhang, Lishan
Zhou, Ying
Luo, Hong
Xu, Huaxi
Wang, Xin
Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title_full Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title_fullStr Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title_full_unstemmed Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title_short Dysregulation of Ubiquitin-Proteasome System in Neurodegenerative Diseases
title_sort dysregulation of ubiquitin-proteasome system in neurodegenerative diseases
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5156861/
https://www.ncbi.nlm.nih.gov/pubmed/28018215
http://dx.doi.org/10.3389/fnagi.2016.00303
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