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Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry
Copper (Cu) is an essential micronutrient for cells, but in excess it is cytotoxic. How Cu is cytotoxic is the subject of recent work by L. Zuily, N. Lahrach, R. Fassler, O. Genest, et al. (mBio 13:e03251-21, 2022, https://doi.org/10.1128/mbio.03251-21). Using Escherichia coli as the model cell, the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239040/ https://www.ncbi.nlm.nih.gov/pubmed/35604220 http://dx.doi.org/10.1128/mbio.00434-22 |
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author | O’Hern, Charlotte I. Z. Djoko, Karrera Y. |
author_facet | O’Hern, Charlotte I. Z. Djoko, Karrera Y. |
author_sort | O’Hern, Charlotte I. Z. |
collection | PubMed |
description | Copper (Cu) is an essential micronutrient for cells, but in excess it is cytotoxic. How Cu is cytotoxic is the subject of recent work by L. Zuily, N. Lahrach, R. Fassler, O. Genest, et al. (mBio 13:e03251-21, 2022, https://doi.org/10.1128/mbio.03251-21). Using Escherichia coli as the model cell, the work shows that anoxic cells accumulate larger amounts of Cu than do oxic cells. Accordingly, Cu is more cytotoxic under anoxic than oxic conditions. The work further shows that Cu cytotoxicity in anoxic bacteria is associated with increased intracellular protein aggregation. The mechanistic details remain as open questions, but these questions highlight that a fundamental understanding of Cu speciation and availability in cells is essential to uncover the cellular consequences of Cu cytotoxicity. |
format | Online Article Text |
id | pubmed-9239040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92390402022-06-29 Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry O’Hern, Charlotte I. Z. Djoko, Karrera Y. mBio Commentary Copper (Cu) is an essential micronutrient for cells, but in excess it is cytotoxic. How Cu is cytotoxic is the subject of recent work by L. Zuily, N. Lahrach, R. Fassler, O. Genest, et al. (mBio 13:e03251-21, 2022, https://doi.org/10.1128/mbio.03251-21). Using Escherichia coli as the model cell, the work shows that anoxic cells accumulate larger amounts of Cu than do oxic cells. Accordingly, Cu is more cytotoxic under anoxic than oxic conditions. The work further shows that Cu cytotoxicity in anoxic bacteria is associated with increased intracellular protein aggregation. The mechanistic details remain as open questions, but these questions highlight that a fundamental understanding of Cu speciation and availability in cells is essential to uncover the cellular consequences of Cu cytotoxicity. American Society for Microbiology 2022-05-23 /pmc/articles/PMC9239040/ /pubmed/35604220 http://dx.doi.org/10.1128/mbio.00434-22 Text en Copyright © 2022 O’Hern and Djoko. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Commentary O’Hern, Charlotte I. Z. Djoko, Karrera Y. Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title | Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title_full | Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title_fullStr | Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title_full_unstemmed | Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title_short | Copper Cytotoxicity: Cellular Casualties of Noncognate Coordination Chemistry |
title_sort | copper cytotoxicity: cellular casualties of noncognate coordination chemistry |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239040/ https://www.ncbi.nlm.nih.gov/pubmed/35604220 http://dx.doi.org/10.1128/mbio.00434-22 |
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