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Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells

Nanoparticles (Nps) can induce toxicity in the lung by accidental or intentional exposure. The main objective of the study reported here was to characterize the effect that four metal oxide Nps (CeO(2), TiO(2), Al(2)O(3) and ZnO) had at the cellular level on a human lung epithelial cell line. This g...

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Autores principales: Simón-Vázquez, Rosana, Lozano-Fernández, Tamara, Dávila-Grana, Angela, González-Fernández, África
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137956/
https://www.ncbi.nlm.nih.gov/pubmed/28031965
http://dx.doi.org/10.4155/fso.16.2
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author Simón-Vázquez, Rosana
Lozano-Fernández, Tamara
Dávila-Grana, Angela
González-Fernández, África
author_facet Simón-Vázquez, Rosana
Lozano-Fernández, Tamara
Dávila-Grana, Angela
González-Fernández, África
author_sort Simón-Vázquez, Rosana
collection PubMed
description Nanoparticles (Nps) can induce toxicity in the lung by accidental or intentional exposure. The main objective of the study reported here was to characterize the effect that four metal oxide Nps (CeO(2), TiO(2), Al(2)O(3) and ZnO) had at the cellular level on a human lung epithelial cell line. This goal was achieved by studying the capacity of the Nps to activate the main mitogen-activated protein kinases (MAPKs) and the nuclear factor NFκB. Only ZnO Nps were able to activate all of the MAPKs and the release of Zn(2+) ions was the main cause of activation. ZnO and Al(2)O(3) Nps activated the NFκB pathway and induced the release of inflammatory cytokines. CeO(2) and TiO(2) Nps were found to have safer profiles. [Image: see text] The graphical abstract was obtained using Servier Medical Art.
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spelling pubmed-51379562016-12-28 Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells Simón-Vázquez, Rosana Lozano-Fernández, Tamara Dávila-Grana, Angela González-Fernández, África Future Sci OA Research Article Nanoparticles (Nps) can induce toxicity in the lung by accidental or intentional exposure. The main objective of the study reported here was to characterize the effect that four metal oxide Nps (CeO(2), TiO(2), Al(2)O(3) and ZnO) had at the cellular level on a human lung epithelial cell line. This goal was achieved by studying the capacity of the Nps to activate the main mitogen-activated protein kinases (MAPKs) and the nuclear factor NFκB. Only ZnO Nps were able to activate all of the MAPKs and the release of Zn(2+) ions was the main cause of activation. ZnO and Al(2)O(3) Nps activated the NFκB pathway and induced the release of inflammatory cytokines. CeO(2) and TiO(2) Nps were found to have safer profiles. [Image: see text] The graphical abstract was obtained using Servier Medical Art. Future Science Ltd 2016-04-15 /pmc/articles/PMC5137956/ /pubmed/28031965 http://dx.doi.org/10.4155/fso.16.2 Text en © Rosana Simón-Vázquez This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Simón-Vázquez, Rosana
Lozano-Fernández, Tamara
Dávila-Grana, Angela
González-Fernández, África
Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title_full Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title_fullStr Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title_full_unstemmed Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title_short Analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
title_sort analysis of the activation routes induced by different metal oxide nanoparticles on human lung epithelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137956/
https://www.ncbi.nlm.nih.gov/pubmed/28031965
http://dx.doi.org/10.4155/fso.16.2
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