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Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)

Titanium dioxide nanoparticles (TiO(2) NPs) have a wide variety of applications in many consumer products, including as food additives, increasing the concern about the possible hazards that TiO(2) NPs may pose to human health. Although most previous studies have focused on the respiratory system, i...

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Autores principales: Brandão, Fátima, Fernández-Bertólez, Natalia, Rosário, Fernanda, Bessa, Maria João, Fraga, Sónia, Pásaro, Eduardo, Teixeira, João Paulo, Laffon, Blanca, Valdiglesias, Vanessa, Costa, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152841/
https://www.ncbi.nlm.nih.gov/pubmed/32120981
http://dx.doi.org/10.3390/nano10030412
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author Brandão, Fátima
Fernández-Bertólez, Natalia
Rosário, Fernanda
Bessa, Maria João
Fraga, Sónia
Pásaro, Eduardo
Teixeira, João Paulo
Laffon, Blanca
Valdiglesias, Vanessa
Costa, Carla
author_facet Brandão, Fátima
Fernández-Bertólez, Natalia
Rosário, Fernanda
Bessa, Maria João
Fraga, Sónia
Pásaro, Eduardo
Teixeira, João Paulo
Laffon, Blanca
Valdiglesias, Vanessa
Costa, Carla
author_sort Brandão, Fátima
collection PubMed
description Titanium dioxide nanoparticles (TiO(2) NPs) have a wide variety of applications in many consumer products, including as food additives, increasing the concern about the possible hazards that TiO(2) NPs may pose to human health. Although most previous studies have focused on the respiratory system, ingestion must also be considered as an important exposure route. Furthermore, after inhalation or ingestion, TiO(2) NPs can reach several organs, such as the liver, brain or lungs. Taking this into consideration, the present study focuses on the uptake and potential genotoxicity (micronuclei induction) of TiO(2) NPs on four human cell lines of diverse origin: lung cells (A549), liver cells (HepG2), glial cells (A172) and neurons (SH-SY5Y), using flow cytometry methods. Results showed a concentration-, time- and cell-type- dependent increase in TiO(2) NPs uptake but no significant induction of micronuclei in any of the tested conditions. Data obtained reinforce the importance of cell model and testing protocols choice for toxicity assessment. However, some questions remain to be answered, namely on the role of cell culture media components on the agglomeration state and mitigation of TiO(2) NPs toxic effects.
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spelling pubmed-71528412020-04-20 Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y) Brandão, Fátima Fernández-Bertólez, Natalia Rosário, Fernanda Bessa, Maria João Fraga, Sónia Pásaro, Eduardo Teixeira, João Paulo Laffon, Blanca Valdiglesias, Vanessa Costa, Carla Nanomaterials (Basel) Article Titanium dioxide nanoparticles (TiO(2) NPs) have a wide variety of applications in many consumer products, including as food additives, increasing the concern about the possible hazards that TiO(2) NPs may pose to human health. Although most previous studies have focused on the respiratory system, ingestion must also be considered as an important exposure route. Furthermore, after inhalation or ingestion, TiO(2) NPs can reach several organs, such as the liver, brain or lungs. Taking this into consideration, the present study focuses on the uptake and potential genotoxicity (micronuclei induction) of TiO(2) NPs on four human cell lines of diverse origin: lung cells (A549), liver cells (HepG2), glial cells (A172) and neurons (SH-SY5Y), using flow cytometry methods. Results showed a concentration-, time- and cell-type- dependent increase in TiO(2) NPs uptake but no significant induction of micronuclei in any of the tested conditions. Data obtained reinforce the importance of cell model and testing protocols choice for toxicity assessment. However, some questions remain to be answered, namely on the role of cell culture media components on the agglomeration state and mitigation of TiO(2) NPs toxic effects. MDPI 2020-02-27 /pmc/articles/PMC7152841/ /pubmed/32120981 http://dx.doi.org/10.3390/nano10030412 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
Brandão, Fátima
Fernández-Bertólez, Natalia
Rosário, Fernanda
Bessa, Maria João
Fraga, Sónia
Pásaro, Eduardo
Teixeira, João Paulo
Laffon, Blanca
Valdiglesias, Vanessa
Costa, Carla
Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title_full Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title_fullStr Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title_full_unstemmed Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title_short Genotoxicity of TiO(2) Nanoparticles in Four Different Human Cell Lines (A549, HEPG2, A172 and SH-SY5Y)
title_sort genotoxicity of tio(2) nanoparticles in four different human cell lines (a549, hepg2, a172 and sh-sy5y)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152841/
https://www.ncbi.nlm.nih.gov/pubmed/32120981
http://dx.doi.org/10.3390/nano10030412
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