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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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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. |
format | Online Article Text |
id | pubmed-5565788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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