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Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells

Metal oxide nanoparticles (NPs) are among the most highly produced nanomaterials, and have many diverse functions in catalysis, environmental remediation, as sensors, and in the production of personal care products. In this study, the toxicity of several widely used metal oxide NPs such as copper ox...

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Detalles Bibliográficos
Autores principales: Sun, Tingting, Yan, Yiwu, Zhao, Yan, Guo, Feng, Jiang, Chengyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423358/
https://www.ncbi.nlm.nih.gov/pubmed/22916263
http://dx.doi.org/10.1371/journal.pone.0043442
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author Sun, Tingting
Yan, Yiwu
Zhao, Yan
Guo, Feng
Jiang, Chengyu
author_facet Sun, Tingting
Yan, Yiwu
Zhao, Yan
Guo, Feng
Jiang, Chengyu
author_sort Sun, Tingting
collection PubMed
description Metal oxide nanoparticles (NPs) are among the most highly produced nanomaterials, and have many diverse functions in catalysis, environmental remediation, as sensors, and in the production of personal care products. In this study, the toxicity of several widely used metal oxide NPs such as copper oxide, silica, titanium oxide and ferric oxide NPs, were evaluated In vitro. We exposed A549, H1650 and CNE-2Z cell lines to metal oxide NPs, and found CuO NPs to be the most toxic, SiO2 mild toxic, while the other metal oxide NPs had little effect on cell viability. Furthermore, the autophagic biomarker LC3-II significantly increased in A549 cells treated with CuO NPs, and the use of the autophagy inhibitors wortmannin and 3-methyladenin significantly improved cell survival. These results indicate that the cytoxicity of CuO NPs may involve the autophagic pathway in A549 cells.
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spelling pubmed-34233582012-08-22 Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells Sun, Tingting Yan, Yiwu Zhao, Yan Guo, Feng Jiang, Chengyu PLoS One Research Article Metal oxide nanoparticles (NPs) are among the most highly produced nanomaterials, and have many diverse functions in catalysis, environmental remediation, as sensors, and in the production of personal care products. In this study, the toxicity of several widely used metal oxide NPs such as copper oxide, silica, titanium oxide and ferric oxide NPs, were evaluated In vitro. We exposed A549, H1650 and CNE-2Z cell lines to metal oxide NPs, and found CuO NPs to be the most toxic, SiO2 mild toxic, while the other metal oxide NPs had little effect on cell viability. Furthermore, the autophagic biomarker LC3-II significantly increased in A549 cells treated with CuO NPs, and the use of the autophagy inhibitors wortmannin and 3-methyladenin significantly improved cell survival. These results indicate that the cytoxicity of CuO NPs may involve the autophagic pathway in A549 cells. Public Library of Science 2012-08-20 /pmc/articles/PMC3423358/ /pubmed/22916263 http://dx.doi.org/10.1371/journal.pone.0043442 Text en © 2012 Sun et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sun, Tingting
Yan, Yiwu
Zhao, Yan
Guo, Feng
Jiang, Chengyu
Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title_full Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title_fullStr Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title_full_unstemmed Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title_short Copper Oxide Nanoparticles Induce Autophagic Cell Death in A549 Cells
title_sort copper oxide nanoparticles induce autophagic cell death in a549 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423358/
https://www.ncbi.nlm.nih.gov/pubmed/22916263
http://dx.doi.org/10.1371/journal.pone.0043442
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