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Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents
Synthetic amorphous silica (SAS) is used in a plethora of applications and included in many daily products to which humans are exposed via inhalation, ingestion, or skin contact. This poses the question of their potential toxicity, particularly towards macrophages, which show specific sensitivity to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408573/ https://www.ncbi.nlm.nih.gov/pubmed/32708108 http://dx.doi.org/10.3390/nano10071418 |
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author | Dussert, Fanny Arthaud, Pierre-Adrien Arnal, Marie-Edith Dalzon, Bastien Torres, Anaëlle Douki, Thierry Herlin, Nathalie Rabilloud, Thierry Carriere, Marie |
author_facet | Dussert, Fanny Arthaud, Pierre-Adrien Arnal, Marie-Edith Dalzon, Bastien Torres, Anaëlle Douki, Thierry Herlin, Nathalie Rabilloud, Thierry Carriere, Marie |
author_sort | Dussert, Fanny |
collection | PubMed |
description | Synthetic amorphous silica (SAS) is used in a plethora of applications and included in many daily products to which humans are exposed via inhalation, ingestion, or skin contact. This poses the question of their potential toxicity, particularly towards macrophages, which show specific sensitivity to this material. SAS represents an ideal candidate for the adsorption of environmental contaminants due to its large surface area and could consequently modulate their toxicity. In this study, we assessed the toxicity towards macrophages and intestinal epithelial cells of three SAS particles, either isolated SiO(2) nanoparticles (LS30) or SiO(2) particles composed of agglomerated-aggregates of fused primary particles, either food-grade (E551) or non-food-grade (Fumed silica). These particles were applied to cells either alone or in combination with genotoxic co-contaminants, i.e., benzo[a]pyrene (B[a]P) and methane methylsulfonate (MMS). We show that macrophages are much more sensitive to these toxic agents than a non-differenciated co-culture of Caco-2 and HT29-MTX cells, used here as a model of intestinal epithelium. Co-exposure to SiO(2) and MMS causes DNA damage in a synergistic way, which is not explained by the modulation of DNA repair protein mRNA expression. Together, this suggests that SiO(2) particles could adsorb genotoxic agents on their surface and, consequently, increase their DNA damaging potential. |
format | Online Article Text |
id | pubmed-7408573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74085732020-08-13 Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents Dussert, Fanny Arthaud, Pierre-Adrien Arnal, Marie-Edith Dalzon, Bastien Torres, Anaëlle Douki, Thierry Herlin, Nathalie Rabilloud, Thierry Carriere, Marie Nanomaterials (Basel) Article Synthetic amorphous silica (SAS) is used in a plethora of applications and included in many daily products to which humans are exposed via inhalation, ingestion, or skin contact. This poses the question of their potential toxicity, particularly towards macrophages, which show specific sensitivity to this material. SAS represents an ideal candidate for the adsorption of environmental contaminants due to its large surface area and could consequently modulate their toxicity. In this study, we assessed the toxicity towards macrophages and intestinal epithelial cells of three SAS particles, either isolated SiO(2) nanoparticles (LS30) or SiO(2) particles composed of agglomerated-aggregates of fused primary particles, either food-grade (E551) or non-food-grade (Fumed silica). These particles were applied to cells either alone or in combination with genotoxic co-contaminants, i.e., benzo[a]pyrene (B[a]P) and methane methylsulfonate (MMS). We show that macrophages are much more sensitive to these toxic agents than a non-differenciated co-culture of Caco-2 and HT29-MTX cells, used here as a model of intestinal epithelium. Co-exposure to SiO(2) and MMS causes DNA damage in a synergistic way, which is not explained by the modulation of DNA repair protein mRNA expression. Together, this suggests that SiO(2) particles could adsorb genotoxic agents on their surface and, consequently, increase their DNA damaging potential. MDPI 2020-07-21 /pmc/articles/PMC7408573/ /pubmed/32708108 http://dx.doi.org/10.3390/nano10071418 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dussert, Fanny Arthaud, Pierre-Adrien Arnal, Marie-Edith Dalzon, Bastien Torres, Anaëlle Douki, Thierry Herlin, Nathalie Rabilloud, Thierry Carriere, Marie Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title | Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title_full | Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title_fullStr | Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title_full_unstemmed | Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title_short | Toxicity to RAW264.7 Macrophages of Silica Nanoparticles and the E551 Food Additive, in Combination with Genotoxic Agents |
title_sort | toxicity to raw264.7 macrophages of silica nanoparticles and the e551 food additive, in combination with genotoxic agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408573/ https://www.ncbi.nlm.nih.gov/pubmed/32708108 http://dx.doi.org/10.3390/nano10071418 |
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