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Recent advances in signal integration mechanisms in the unfolded protein response
Since its discovery more than 25 years ago, great progress has been made in our understanding of the unfolded protein response (UPR), a homeostatic mechanism that adjusts endoplasmic reticulum (ER) function to satisfy the physiological demands of the cell. However, if ER homeostasis is unattainable,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833987/ https://www.ncbi.nlm.nih.gov/pubmed/31723416 http://dx.doi.org/10.12688/f1000research.19848.1 |
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author | Karagöz, G. Elif Aragón, Tomás Acosta-Alvear, Diego |
author_facet | Karagöz, G. Elif Aragón, Tomás Acosta-Alvear, Diego |
author_sort | Karagöz, G. Elif |
collection | PubMed |
description | Since its discovery more than 25 years ago, great progress has been made in our understanding of the unfolded protein response (UPR), a homeostatic mechanism that adjusts endoplasmic reticulum (ER) function to satisfy the physiological demands of the cell. However, if ER homeostasis is unattainable, the UPR switches to drive cell death to remove defective cells in an effort to protect the health of the organism. This functional dichotomy places the UPR at the crossroads of the adaptation versus apoptosis decision. Here, we focus on new developments in UPR signaling mechanisms, in the interconnectivity among the signaling pathways that make up the UPR in higher eukaryotes, and in the coordination between the UPR and other fundamental cellular processes. |
format | Online Article Text |
id | pubmed-6833987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-68339872019-11-12 Recent advances in signal integration mechanisms in the unfolded protein response Karagöz, G. Elif Aragón, Tomás Acosta-Alvear, Diego F1000Res Review Since its discovery more than 25 years ago, great progress has been made in our understanding of the unfolded protein response (UPR), a homeostatic mechanism that adjusts endoplasmic reticulum (ER) function to satisfy the physiological demands of the cell. However, if ER homeostasis is unattainable, the UPR switches to drive cell death to remove defective cells in an effort to protect the health of the organism. This functional dichotomy places the UPR at the crossroads of the adaptation versus apoptosis decision. Here, we focus on new developments in UPR signaling mechanisms, in the interconnectivity among the signaling pathways that make up the UPR in higher eukaryotes, and in the coordination between the UPR and other fundamental cellular processes. F1000 Research Limited 2019-11-01 /pmc/articles/PMC6833987/ /pubmed/31723416 http://dx.doi.org/10.12688/f1000research.19848.1 Text en Copyright: © 2019 Karagöz GE et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Karagöz, G. Elif Aragón, Tomás Acosta-Alvear, Diego Recent advances in signal integration mechanisms in the unfolded protein response |
title | Recent advances in signal integration mechanisms in the unfolded protein response |
title_full | Recent advances in signal integration mechanisms in the unfolded protein response |
title_fullStr | Recent advances in signal integration mechanisms in the unfolded protein response |
title_full_unstemmed | Recent advances in signal integration mechanisms in the unfolded protein response |
title_short | Recent advances in signal integration mechanisms in the unfolded protein response |
title_sort | recent advances in signal integration mechanisms in the unfolded protein response |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833987/ https://www.ncbi.nlm.nih.gov/pubmed/31723416 http://dx.doi.org/10.12688/f1000research.19848.1 |
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