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Regulation of basal cellular physiology by the homeostatic unfolded protein response

The extensive membrane network of the endoplasmic reticulum (ER) is physically juxtaposed to and functionally entwined with essentially all other cellular compartments. Therefore, the ER must sense diverse and constantly changing physiological inputs so it can adjust its numerous functions to mainta...

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Detalles Bibliográficos
Autores principales: Rutkowski, D. Thomas, Hegde, Ramanujan S.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878945/
https://www.ncbi.nlm.nih.gov/pubmed/20513765
http://dx.doi.org/10.1083/jcb.201003138
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author Rutkowski, D. Thomas
Hegde, Ramanujan S.
author_facet Rutkowski, D. Thomas
Hegde, Ramanujan S.
author_sort Rutkowski, D. Thomas
collection PubMed
description The extensive membrane network of the endoplasmic reticulum (ER) is physically juxtaposed to and functionally entwined with essentially all other cellular compartments. Therefore, the ER must sense diverse and constantly changing physiological inputs so it can adjust its numerous functions to maintain cellular homeostasis. A growing body of new work suggests that the unfolded protein response (UPR), traditionally charged with signaling protein misfolding stress from the ER, has been co-opted for the maintenance of basal cellular homeostasis. Thus, the UPR can be activated, and its output modulated, by signals far outside the realm of protein misfolding. These findings are revealing that the UPR causally contributes to disease not just by its role in protein folding but also through its broad influence on cellular physiology.
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spelling pubmed-28789452010-11-30 Regulation of basal cellular physiology by the homeostatic unfolded protein response Rutkowski, D. Thomas Hegde, Ramanujan S. J Cell Biol Reviews The extensive membrane network of the endoplasmic reticulum (ER) is physically juxtaposed to and functionally entwined with essentially all other cellular compartments. Therefore, the ER must sense diverse and constantly changing physiological inputs so it can adjust its numerous functions to maintain cellular homeostasis. A growing body of new work suggests that the unfolded protein response (UPR), traditionally charged with signaling protein misfolding stress from the ER, has been co-opted for the maintenance of basal cellular homeostasis. Thus, the UPR can be activated, and its output modulated, by signals far outside the realm of protein misfolding. These findings are revealing that the UPR causally contributes to disease not just by its role in protein folding but also through its broad influence on cellular physiology. The Rockefeller University Press 2010-05-31 /pmc/articles/PMC2878945/ /pubmed/20513765 http://dx.doi.org/10.1083/jcb.201003138 Text en © 2010 Rutkowski and Hegde This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Reviews
Rutkowski, D. Thomas
Hegde, Ramanujan S.
Regulation of basal cellular physiology by the homeostatic unfolded protein response
title Regulation of basal cellular physiology by the homeostatic unfolded protein response
title_full Regulation of basal cellular physiology by the homeostatic unfolded protein response
title_fullStr Regulation of basal cellular physiology by the homeostatic unfolded protein response
title_full_unstemmed Regulation of basal cellular physiology by the homeostatic unfolded protein response
title_short Regulation of basal cellular physiology by the homeostatic unfolded protein response
title_sort regulation of basal cellular physiology by the homeostatic unfolded protein response
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878945/
https://www.ncbi.nlm.nih.gov/pubmed/20513765
http://dx.doi.org/10.1083/jcb.201003138
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