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Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets

Graphene nanomaterials have attracted a great interest during the last years for different applications, but their possible impact on different biological systems remains unclear. Here, an assessment to understand the toxicity of commercial polycarboxylate functionalized graphene nanoplatelets (GN)...

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Autores principales: Suarez-Diez, Maria, Porras, Santiago, Laguna-Teno, Felix, Schaap, Peter J., Tamayo-Ramos, Juan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039959/
https://www.ncbi.nlm.nih.gov/pubmed/32094381
http://dx.doi.org/10.1038/s41598-020-60101-7
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author Suarez-Diez, Maria
Porras, Santiago
Laguna-Teno, Felix
Schaap, Peter J.
Tamayo-Ramos, Juan A.
author_facet Suarez-Diez, Maria
Porras, Santiago
Laguna-Teno, Felix
Schaap, Peter J.
Tamayo-Ramos, Juan A.
author_sort Suarez-Diez, Maria
collection PubMed
description Graphene nanomaterials have attracted a great interest during the last years for different applications, but their possible impact on different biological systems remains unclear. Here, an assessment to understand the toxicity of commercial polycarboxylate functionalized graphene nanoplatelets (GN) on the unicellular fungal model Saccharomyces cerevisiae was performed. While cell proliferation was not negatively affected even in the presence of 800 mg L(−1) of the nanomaterial for 24 hours, oxidative stress was induced at a lower concentration (160 mg L(−1)), after short exposure periods (2 and 4 hours). No DNA damage was observed under a comet assay analysis under the studied conditions. In addition, to pinpoint the molecular mechanisms behind the early oxidative damage induced by GN and to identify possible toxicity pathways, the transcriptome of S. cerevisiae exposed to 160 and 800 mg L(−1) of GN was studied. Both GN concentrations induced expression changes in a common group of genes (337), many of them related to the fungal response to reduce the nanoparticles toxicity and to maintain cell homeostasis. Also, a high number of genes were only differentially expressed in the GN800 condition (3254), indicating that high GN concentrations can induce severe changes in the physiological state of the yeast.
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spelling pubmed-70399592020-02-28 Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets Suarez-Diez, Maria Porras, Santiago Laguna-Teno, Felix Schaap, Peter J. Tamayo-Ramos, Juan A. Sci Rep Article Graphene nanomaterials have attracted a great interest during the last years for different applications, but their possible impact on different biological systems remains unclear. Here, an assessment to understand the toxicity of commercial polycarboxylate functionalized graphene nanoplatelets (GN) on the unicellular fungal model Saccharomyces cerevisiae was performed. While cell proliferation was not negatively affected even in the presence of 800 mg L(−1) of the nanomaterial for 24 hours, oxidative stress was induced at a lower concentration (160 mg L(−1)), after short exposure periods (2 and 4 hours). No DNA damage was observed under a comet assay analysis under the studied conditions. In addition, to pinpoint the molecular mechanisms behind the early oxidative damage induced by GN and to identify possible toxicity pathways, the transcriptome of S. cerevisiae exposed to 160 and 800 mg L(−1) of GN was studied. Both GN concentrations induced expression changes in a common group of genes (337), many of them related to the fungal response to reduce the nanoparticles toxicity and to maintain cell homeostasis. Also, a high number of genes were only differentially expressed in the GN800 condition (3254), indicating that high GN concentrations can induce severe changes in the physiological state of the yeast. Nature Publishing Group UK 2020-02-24 /pmc/articles/PMC7039959/ /pubmed/32094381 http://dx.doi.org/10.1038/s41598-020-60101-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Suarez-Diez, Maria
Porras, Santiago
Laguna-Teno, Felix
Schaap, Peter J.
Tamayo-Ramos, Juan A.
Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title_full Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title_fullStr Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title_full_unstemmed Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title_short Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
title_sort toxicological response of the model fungus saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039959/
https://www.ncbi.nlm.nih.gov/pubmed/32094381
http://dx.doi.org/10.1038/s41598-020-60101-7
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