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Ubiquitin-Proteasome System in Neurodegenerative Disorders

Cellular proteostasis is a highly dynamic process and is primarily carried out by the degradation tools of ubiquitin-proteasome system (UPS). Abnormalities in UPS function result in the accumulation of damaged or misfolded proteins which can form intra- and extracellular aggregated proteinaceous dep...

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Detalles Bibliográficos
Autores principales: Rao, Geeta, Croft, Brandon, Teng, Chengwen, Awasthi, Vibhudutta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370320/
https://www.ncbi.nlm.nih.gov/pubmed/30761219
http://dx.doi.org/10.4172/2157-7609.1000187
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author Rao, Geeta
Croft, Brandon
Teng, Chengwen
Awasthi, Vibhudutta
author_facet Rao, Geeta
Croft, Brandon
Teng, Chengwen
Awasthi, Vibhudutta
author_sort Rao, Geeta
collection PubMed
description Cellular proteostasis is a highly dynamic process and is primarily carried out by the degradation tools of ubiquitin-proteasome system (UPS). Abnormalities in UPS function result in the accumulation of damaged or misfolded proteins which can form intra- and extracellular aggregated proteinaceous deposits leading to cellular dysfunction and/or death. Deposition of abnormal protein aggregates and the cellular inability to clear them have been implicated in the pathogenesis of a number of neurodegenerative disorders such as Alzheimer’s and Parkinson’s. Contrary to the upregulation of proteasome function in oncogenesis and the use of proteasome inhibition as a therapeutic strategy, activation of proteasome function would serve therapeutic objectives of treatment of neurodegenerative diseases. This review describes the current understanding of the role of the proteasome in neurodegenerative disorders and potential utility of proteasomal modulation therein.
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spelling pubmed-63703202019-02-11 Ubiquitin-Proteasome System in Neurodegenerative Disorders Rao, Geeta Croft, Brandon Teng, Chengwen Awasthi, Vibhudutta J Drug Metab Toxicol Article Cellular proteostasis is a highly dynamic process and is primarily carried out by the degradation tools of ubiquitin-proteasome system (UPS). Abnormalities in UPS function result in the accumulation of damaged or misfolded proteins which can form intra- and extracellular aggregated proteinaceous deposits leading to cellular dysfunction and/or death. Deposition of abnormal protein aggregates and the cellular inability to clear them have been implicated in the pathogenesis of a number of neurodegenerative disorders such as Alzheimer’s and Parkinson’s. Contrary to the upregulation of proteasome function in oncogenesis and the use of proteasome inhibition as a therapeutic strategy, activation of proteasome function would serve therapeutic objectives of treatment of neurodegenerative diseases. This review describes the current understanding of the role of the proteasome in neurodegenerative disorders and potential utility of proteasomal modulation therein. 2015-08-13 2015 /pmc/articles/PMC6370320/ /pubmed/30761219 http://dx.doi.org/10.4172/2157-7609.1000187 Text en This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Rao, Geeta
Croft, Brandon
Teng, Chengwen
Awasthi, Vibhudutta
Ubiquitin-Proteasome System in Neurodegenerative Disorders
title Ubiquitin-Proteasome System in Neurodegenerative Disorders
title_full Ubiquitin-Proteasome System in Neurodegenerative Disorders
title_fullStr Ubiquitin-Proteasome System in Neurodegenerative Disorders
title_full_unstemmed Ubiquitin-Proteasome System in Neurodegenerative Disorders
title_short Ubiquitin-Proteasome System in Neurodegenerative Disorders
title_sort ubiquitin-proteasome system in neurodegenerative disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370320/
https://www.ncbi.nlm.nih.gov/pubmed/30761219
http://dx.doi.org/10.4172/2157-7609.1000187
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