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The UPR in Neurodegenerative Disease: Not Just an Inside Job

Neurons are highly specialized cells that continuously and extensively communicate with other neurons, as well as glia cells. During their long lifetime, the post-mitotic neurons encounter many stressful situations that can disrupt protein homeostasis (proteostasis). The importance of tight protein...

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Autores principales: van Ziel, Anna Maria, Scheper, Wiep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465596/
https://www.ncbi.nlm.nih.gov/pubmed/32707908
http://dx.doi.org/10.3390/biom10081090
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author van Ziel, Anna Maria
Scheper, Wiep
author_facet van Ziel, Anna Maria
Scheper, Wiep
author_sort van Ziel, Anna Maria
collection PubMed
description Neurons are highly specialized cells that continuously and extensively communicate with other neurons, as well as glia cells. During their long lifetime, the post-mitotic neurons encounter many stressful situations that can disrupt protein homeostasis (proteostasis). The importance of tight protein quality control is illustrated by neurodegenerative disorders where disturbed neuronal proteostasis causes neuronal dysfunction and loss. For their unique function, neurons require regulated and long-distance transport of membrane-bound cargo and organelles. This highlights the importance of protein quality control in the neuronal endomembrane system, to which the unfolded protein response (UPR) is instrumental. The UPR is a highly conserved stress response that is present in all eukaryotes. However, recent studies demonstrate the existence of cell-type-specific aspects of the UPR, as well as cell non-autonomous UPR signaling. Here we discuss these novel insights in view of the complex cellular architecture of the brain and the implications for neurodegenerative diseases.
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spelling pubmed-74655962020-09-04 The UPR in Neurodegenerative Disease: Not Just an Inside Job van Ziel, Anna Maria Scheper, Wiep Biomolecules Review Neurons are highly specialized cells that continuously and extensively communicate with other neurons, as well as glia cells. During their long lifetime, the post-mitotic neurons encounter many stressful situations that can disrupt protein homeostasis (proteostasis). The importance of tight protein quality control is illustrated by neurodegenerative disorders where disturbed neuronal proteostasis causes neuronal dysfunction and loss. For their unique function, neurons require regulated and long-distance transport of membrane-bound cargo and organelles. This highlights the importance of protein quality control in the neuronal endomembrane system, to which the unfolded protein response (UPR) is instrumental. The UPR is a highly conserved stress response that is present in all eukaryotes. However, recent studies demonstrate the existence of cell-type-specific aspects of the UPR, as well as cell non-autonomous UPR signaling. Here we discuss these novel insights in view of the complex cellular architecture of the brain and the implications for neurodegenerative diseases. MDPI 2020-07-22 /pmc/articles/PMC7465596/ /pubmed/32707908 http://dx.doi.org/10.3390/biom10081090 Text en © 2020 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
van Ziel, Anna Maria
Scheper, Wiep
The UPR in Neurodegenerative Disease: Not Just an Inside Job
title The UPR in Neurodegenerative Disease: Not Just an Inside Job
title_full The UPR in Neurodegenerative Disease: Not Just an Inside Job
title_fullStr The UPR in Neurodegenerative Disease: Not Just an Inside Job
title_full_unstemmed The UPR in Neurodegenerative Disease: Not Just an Inside Job
title_short The UPR in Neurodegenerative Disease: Not Just an Inside Job
title_sort upr in neurodegenerative disease: not just an inside job
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465596/
https://www.ncbi.nlm.nih.gov/pubmed/32707908
http://dx.doi.org/10.3390/biom10081090
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