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The unfolded protein response in multiple sclerosis

The unfolded protein response (UPR) occurs in response to endoplasmic reticulum (ER) stress caused by the accumulation of unfolded or misfolded proteins in the ER. The UPR is comprised of three signaling pathways that promote cytoprotective functions to correct ER stress; however, if ER stress canno...

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Detalles Bibliográficos
Autores principales: Stone, Sarrabeth, Lin, Wensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518158/
https://www.ncbi.nlm.nih.gov/pubmed/26283904
http://dx.doi.org/10.3389/fnins.2015.00264
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author Stone, Sarrabeth
Lin, Wensheng
author_facet Stone, Sarrabeth
Lin, Wensheng
author_sort Stone, Sarrabeth
collection PubMed
description The unfolded protein response (UPR) occurs in response to endoplasmic reticulum (ER) stress caused by the accumulation of unfolded or misfolded proteins in the ER. The UPR is comprised of three signaling pathways that promote cytoprotective functions to correct ER stress; however, if ER stress cannot be resolved the UPR results in apoptosis of affected cells. The UPR is an important feature of various human diseases, including multiple sclerosis (MS). Recent studies have shown several components of the UPR are upregulated in the multiple cell types in MS lesions, including oligodendrocytes, T cells, microglia/macrophages, and astrocytes. Data from animal model studies, particularly studies of experimental autoimmune encephalomyelitis (EAE) and the cuprizone model, imply an important role of the UPR activation in oligodendrocytes in the development of MS. In this review we will cover current literature on the UPR and the evidence for its role in the development of MS.
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spelling pubmed-45181582015-08-17 The unfolded protein response in multiple sclerosis Stone, Sarrabeth Lin, Wensheng Front Neurosci Psychiatry The unfolded protein response (UPR) occurs in response to endoplasmic reticulum (ER) stress caused by the accumulation of unfolded or misfolded proteins in the ER. The UPR is comprised of three signaling pathways that promote cytoprotective functions to correct ER stress; however, if ER stress cannot be resolved the UPR results in apoptosis of affected cells. The UPR is an important feature of various human diseases, including multiple sclerosis (MS). Recent studies have shown several components of the UPR are upregulated in the multiple cell types in MS lesions, including oligodendrocytes, T cells, microglia/macrophages, and astrocytes. Data from animal model studies, particularly studies of experimental autoimmune encephalomyelitis (EAE) and the cuprizone model, imply an important role of the UPR activation in oligodendrocytes in the development of MS. In this review we will cover current literature on the UPR and the evidence for its role in the development of MS. Frontiers Media S.A. 2015-07-29 /pmc/articles/PMC4518158/ /pubmed/26283904 http://dx.doi.org/10.3389/fnins.2015.00264 Text en Copyright © 2015 Stone and Lin. 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 Psychiatry
Stone, Sarrabeth
Lin, Wensheng
The unfolded protein response in multiple sclerosis
title The unfolded protein response in multiple sclerosis
title_full The unfolded protein response in multiple sclerosis
title_fullStr The unfolded protein response in multiple sclerosis
title_full_unstemmed The unfolded protein response in multiple sclerosis
title_short The unfolded protein response in multiple sclerosis
title_sort unfolded protein response in multiple sclerosis
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518158/
https://www.ncbi.nlm.nih.gov/pubmed/26283904
http://dx.doi.org/10.3389/fnins.2015.00264
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