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Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition

The ubiquitin-proteasome system targets many cellular proteins for degradation and thereby controls most cellular processes. Although it is well established that proteasome inhibition is lethal, the underlying mechanism is unknown. Here, we show that proteasome inhibition results in a lethal amino a...

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Detalles Bibliográficos
Autores principales: Suraweera, Amila, Münch, Christian, Hanssum, Ariane, Bertolotti, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482661/
https://www.ncbi.nlm.nih.gov/pubmed/22959274
http://dx.doi.org/10.1016/j.molcel.2012.08.003
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author Suraweera, Amila
Münch, Christian
Hanssum, Ariane
Bertolotti, Anne
author_facet Suraweera, Amila
Münch, Christian
Hanssum, Ariane
Bertolotti, Anne
author_sort Suraweera, Amila
collection PubMed
description The ubiquitin-proteasome system targets many cellular proteins for degradation and thereby controls most cellular processes. Although it is well established that proteasome inhibition is lethal, the underlying mechanism is unknown. Here, we show that proteasome inhibition results in a lethal amino acid shortage. In yeast, mammalian cells, and flies, the deleterious consequences of proteasome inhibition are rescued by amino acid supplementation. In all three systems, this rescuing effect occurs without noticeable changes in the levels of proteasome substrates. In mammalian cells, the amino acid scarcity resulting from proteasome inhibition is the signal that causes induction of both the integrated stress response and autophagy, in an unsuccessful attempt to replenish the pool of intracellular amino acids. These results reveal that cells can tolerate protein waste, but not the amino acid scarcity resulting from proteasome inhibition.
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spelling pubmed-34826612012-11-14 Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition Suraweera, Amila Münch, Christian Hanssum, Ariane Bertolotti, Anne Mol Cell Article The ubiquitin-proteasome system targets many cellular proteins for degradation and thereby controls most cellular processes. Although it is well established that proteasome inhibition is lethal, the underlying mechanism is unknown. Here, we show that proteasome inhibition results in a lethal amino acid shortage. In yeast, mammalian cells, and flies, the deleterious consequences of proteasome inhibition are rescued by amino acid supplementation. In all three systems, this rescuing effect occurs without noticeable changes in the levels of proteasome substrates. In mammalian cells, the amino acid scarcity resulting from proteasome inhibition is the signal that causes induction of both the integrated stress response and autophagy, in an unsuccessful attempt to replenish the pool of intracellular amino acids. These results reveal that cells can tolerate protein waste, but not the amino acid scarcity resulting from proteasome inhibition. Cell Press 2012-10-26 /pmc/articles/PMC3482661/ /pubmed/22959274 http://dx.doi.org/10.1016/j.molcel.2012.08.003 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Suraweera, Amila
Münch, Christian
Hanssum, Ariane
Bertolotti, Anne
Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title_full Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title_fullStr Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title_full_unstemmed Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title_short Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition
title_sort failure of amino acid homeostasis causes cell death following proteasome inhibition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482661/
https://www.ncbi.nlm.nih.gov/pubmed/22959274
http://dx.doi.org/10.1016/j.molcel.2012.08.003
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