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The Role of IRE1 Signaling in the Central Nervous System Diseases

The accumulation of misfolded or unfolded proteins in endoplasmic reticulum (ER) lumen results in the activation of an adaptive stress process called the unfolded protein response (UPR). As the most conserved signaling branch of the UPR, Inositol-requiring enzyme 1 (IRE1) possesses both Ser/Thr kina...

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Detalles Bibliográficos
Autores principales: Ni, Haibo, Rui, Qin, Li, Di, Gao, Rong, Chen, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251047/
https://www.ncbi.nlm.nih.gov/pubmed/29663887
http://dx.doi.org/10.2174/1570159X16666180416094646
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author Ni, Haibo
Rui, Qin
Li, Di
Gao, Rong
Chen, Gang
author_facet Ni, Haibo
Rui, Qin
Li, Di
Gao, Rong
Chen, Gang
author_sort Ni, Haibo
collection PubMed
description The accumulation of misfolded or unfolded proteins in endoplasmic reticulum (ER) lumen results in the activation of an adaptive stress process called the unfolded protein response (UPR). As the most conserved signaling branch of the UPR, Inositol-requiring enzyme 1 (IRE1) possesses both Ser/Thr kinase and RNase activities operating as major stress sensors, mediating both adaptive and pro-apoptotic pathways under ER stress. Over the last three decades, a mounting body of evidence has shown that IRE1 signaling dysfunction is involved in the pathology of various neurological disorders. Tar-geting this pathway has emerged as a promising therapeutic strategy against these diseases. In this review, we provide a gen-eral overview about the expression and physiological function of IRE1 signaling and its pathophysiological roles in the cen-tral nervous system diseases.
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spelling pubmed-62510472019-05-01 The Role of IRE1 Signaling in the Central Nervous System Diseases Ni, Haibo Rui, Qin Li, Di Gao, Rong Chen, Gang Curr Neuropharmacol Article The accumulation of misfolded or unfolded proteins in endoplasmic reticulum (ER) lumen results in the activation of an adaptive stress process called the unfolded protein response (UPR). As the most conserved signaling branch of the UPR, Inositol-requiring enzyme 1 (IRE1) possesses both Ser/Thr kinase and RNase activities operating as major stress sensors, mediating both adaptive and pro-apoptotic pathways under ER stress. Over the last three decades, a mounting body of evidence has shown that IRE1 signaling dysfunction is involved in the pathology of various neurological disorders. Tar-geting this pathway has emerged as a promising therapeutic strategy against these diseases. In this review, we provide a gen-eral overview about the expression and physiological function of IRE1 signaling and its pathophysiological roles in the cen-tral nervous system diseases. Bentham Science Publishers 2018-11 2018-11 /pmc/articles/PMC6251047/ /pubmed/29663887 http://dx.doi.org/10.2174/1570159X16666180416094646 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Ni, Haibo
Rui, Qin
Li, Di
Gao, Rong
Chen, Gang
The Role of IRE1 Signaling in the Central Nervous System Diseases
title The Role of IRE1 Signaling in the Central Nervous System Diseases
title_full The Role of IRE1 Signaling in the Central Nervous System Diseases
title_fullStr The Role of IRE1 Signaling in the Central Nervous System Diseases
title_full_unstemmed The Role of IRE1 Signaling in the Central Nervous System Diseases
title_short The Role of IRE1 Signaling in the Central Nervous System Diseases
title_sort role of ire1 signaling in the central nervous system diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251047/
https://www.ncbi.nlm.nih.gov/pubmed/29663887
http://dx.doi.org/10.2174/1570159X16666180416094646
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