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Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux

Energy production is inevitably linked to the generation of toxic metabolites, such as reactive oxygen and carbonyl species, known as major contributors to ageing and degenerative diseases. It remains unclear how cells can adapt to elevated energy flux accompanied by accumulating harmful by-products...

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Autores principales: Zemva, Johanna, Fink, Christoph Andreas, Fleming, Thomas Henry, Schmidt, Leonard, Loft, Anne, Herzig, Stephan, Knieß, Robert André, Mayer, Matthias, Bukau, Bernd, Nawroth, Peter Paul, Tyedmers, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565788/
https://www.ncbi.nlm.nih.gov/pubmed/28826004
http://dx.doi.org/10.1016/j.redox.2017.08.007
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author Zemva, Johanna
Fink, Christoph Andreas
Fleming, Thomas Henry
Schmidt, Leonard
Loft, Anne
Herzig, Stephan
Knieß, Robert André
Mayer, Matthias
Bukau, Bernd
Nawroth, Peter Paul
Tyedmers, Jens
author_facet Zemva, Johanna
Fink, Christoph Andreas
Fleming, Thomas Henry
Schmidt, Leonard
Loft, Anne
Herzig, Stephan
Knieß, Robert André
Mayer, Matthias
Bukau, Bernd
Nawroth, Peter Paul
Tyedmers, Jens
author_sort Zemva, Johanna
collection PubMed
description Energy production is inevitably linked to the generation of toxic metabolites, such as reactive oxygen and carbonyl species, known as major contributors to ageing and degenerative diseases. It remains unclear how cells can adapt to elevated energy flux accompanied by accumulating harmful by-products without taking any damage. Therefore, effects of a sudden rise in glucose concentrations were studied in yeast cells. This revealed a feedback mechanism initiated by the reactive dicarbonyl methylglyoxal, which is formed non-enzymatically during glycolysis. Low levels of methylglyoxal activate a multi-layered defence response against toxic metabolites composed of prevention, detoxification and damage remission. The latter is mediated by the protein quality control system and requires inducible Hsp70 and Btn2, the aggregase that sequesters misfolded proteins. This glycohormetic mechanism enables cells to pre-adapt to rising energy flux and directly links metabolic to proteotoxic stress. Further data suggest the existence of a similar response in endothelial cells.
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spelling pubmed-55657882017-08-31 Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux Zemva, Johanna Fink, Christoph Andreas Fleming, Thomas Henry Schmidt, Leonard Loft, Anne Herzig, Stephan Knieß, Robert André Mayer, Matthias Bukau, Bernd Nawroth, Peter Paul Tyedmers, Jens Redox Biol Research Paper Energy production is inevitably linked to the generation of toxic metabolites, such as reactive oxygen and carbonyl species, known as major contributors to ageing and degenerative diseases. It remains unclear how cells can adapt to elevated energy flux accompanied by accumulating harmful by-products without taking any damage. Therefore, effects of a sudden rise in glucose concentrations were studied in yeast cells. This revealed a feedback mechanism initiated by the reactive dicarbonyl methylglyoxal, which is formed non-enzymatically during glycolysis. Low levels of methylglyoxal activate a multi-layered defence response against toxic metabolites composed of prevention, detoxification and damage remission. The latter is mediated by the protein quality control system and requires inducible Hsp70 and Btn2, the aggregase that sequesters misfolded proteins. This glycohormetic mechanism enables cells to pre-adapt to rising energy flux and directly links metabolic to proteotoxic stress. Further data suggest the existence of a similar response in endothelial cells. Elsevier 2017-08-12 /pmc/articles/PMC5565788/ /pubmed/28826004 http://dx.doi.org/10.1016/j.redox.2017.08.007 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Zemva, Johanna
Fink, Christoph Andreas
Fleming, Thomas Henry
Schmidt, Leonard
Loft, Anne
Herzig, Stephan
Knieß, Robert André
Mayer, Matthias
Bukau, Bernd
Nawroth, Peter Paul
Tyedmers, Jens
Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title_full Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title_fullStr Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title_full_unstemmed Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title_short Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
title_sort hormesis enables cells to handle accumulating toxic metabolites during increased energy flux
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5565788/
https://www.ncbi.nlm.nih.gov/pubmed/28826004
http://dx.doi.org/10.1016/j.redox.2017.08.007
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