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Molecular analysis of chromium and cobalt-related toxicity
Occupational and environmental exposure to Co and Cr has been previously linked to a wide array of inflammatory and degenerative conditions and cancer. Recently, significant health concerns have been raised by the high levels of Cr and Co ions and corrosion products released by biomedical implants....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103093/ https://www.ncbi.nlm.nih.gov/pubmed/25034144 http://dx.doi.org/10.1038/srep05729 |
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author | Scharf, Brian Clement, Cristina C. Zolla, Valerio Perino, Giorgio Yan, Bo Elci, S. Gokhan Purdue, E. Goldring, S. Macaluso, Frank Cobelli, Neil Vachet, Richard W. Santambrogio, Laura |
author_facet | Scharf, Brian Clement, Cristina C. Zolla, Valerio Perino, Giorgio Yan, Bo Elci, S. Gokhan Purdue, E. Goldring, S. Macaluso, Frank Cobelli, Neil Vachet, Richard W. Santambrogio, Laura |
author_sort | Scharf, Brian |
collection | PubMed |
description | Occupational and environmental exposure to Co and Cr has been previously linked to a wide array of inflammatory and degenerative conditions and cancer. Recently, significant health concerns have been raised by the high levels of Cr and Co ions and corrosion products released by biomedical implants. Herein, we set to analyze the biological responses associated with Co and Cr toxicity. Histological, ultrastructural, and elemental analysis, performed on Cr and Co exposed patients reveal the presence of corrosion products, metallic wear debris and metal ions at varying concentrations. Metallic ions and corrosion products were also generated in vitro following macrophage phagocytosis of metal alloys. Ex vivo redox proteomic mapped several oxidatively damaged proteins by Cr(III) and Co(II)-induced Fenton reaction. Importantly, a positive correlation between the tissue amounts of Cr(III) and Co(II) ions and tissue oxidative damage was observed. Immobilized- Cr(III) and Co(II) affinity chromatography indicated that metal ions can also directly bind to several metallo and non-metalloproteins and, as demonstrated for aldolase and catalase, induce loss of their biological function. Altogether, our analysis reveals several biological mechanisms leading to tissue damage, necrosis, and inflammation in patients with Cr and Co-associated adverse local tissue reactions. |
format | Online Article Text |
id | pubmed-4103093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41030932014-07-21 Molecular analysis of chromium and cobalt-related toxicity Scharf, Brian Clement, Cristina C. Zolla, Valerio Perino, Giorgio Yan, Bo Elci, S. Gokhan Purdue, E. Goldring, S. Macaluso, Frank Cobelli, Neil Vachet, Richard W. Santambrogio, Laura Sci Rep Article Occupational and environmental exposure to Co and Cr has been previously linked to a wide array of inflammatory and degenerative conditions and cancer. Recently, significant health concerns have been raised by the high levels of Cr and Co ions and corrosion products released by biomedical implants. Herein, we set to analyze the biological responses associated with Co and Cr toxicity. Histological, ultrastructural, and elemental analysis, performed on Cr and Co exposed patients reveal the presence of corrosion products, metallic wear debris and metal ions at varying concentrations. Metallic ions and corrosion products were also generated in vitro following macrophage phagocytosis of metal alloys. Ex vivo redox proteomic mapped several oxidatively damaged proteins by Cr(III) and Co(II)-induced Fenton reaction. Importantly, a positive correlation between the tissue amounts of Cr(III) and Co(II) ions and tissue oxidative damage was observed. Immobilized- Cr(III) and Co(II) affinity chromatography indicated that metal ions can also directly bind to several metallo and non-metalloproteins and, as demonstrated for aldolase and catalase, induce loss of their biological function. Altogether, our analysis reveals several biological mechanisms leading to tissue damage, necrosis, and inflammation in patients with Cr and Co-associated adverse local tissue reactions. Nature Publishing Group 2014-07-17 /pmc/articles/PMC4103093/ /pubmed/25034144 http://dx.doi.org/10.1038/srep05729 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Scharf, Brian Clement, Cristina C. Zolla, Valerio Perino, Giorgio Yan, Bo Elci, S. Gokhan Purdue, E. Goldring, S. Macaluso, Frank Cobelli, Neil Vachet, Richard W. Santambrogio, Laura Molecular analysis of chromium and cobalt-related toxicity |
title | Molecular analysis of chromium and cobalt-related toxicity |
title_full | Molecular analysis of chromium and cobalt-related toxicity |
title_fullStr | Molecular analysis of chromium and cobalt-related toxicity |
title_full_unstemmed | Molecular analysis of chromium and cobalt-related toxicity |
title_short | Molecular analysis of chromium and cobalt-related toxicity |
title_sort | molecular analysis of chromium and cobalt-related toxicity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103093/ https://www.ncbi.nlm.nih.gov/pubmed/25034144 http://dx.doi.org/10.1038/srep05729 |
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