DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles

The genotoxicity of nanomaterials has attracted great attention in recent years. As a possible occupational carcinogen, the genotoxic effects and underlying mechanisms of titanium dioxide nanoparticles (TiO<sub>2</sub> NPs) have been of particular concern. In this study, the effect of Ti...

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Main Authors: Zhangjian Chen, Jiaqi Shi, Yi Zhang, Shuo Han, Jiahe Zhang, Guang Jia
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/12/15/2616
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author Zhangjian Chen
Jiaqi Shi
Yi Zhang
Shuo Han
Jiahe Zhang
Guang Jia
author_facet Zhangjian Chen
Jiaqi Shi
Yi Zhang
Shuo Han
Jiahe Zhang
Guang Jia
author_sort Zhangjian Chen
collection DOAJ
description The genotoxicity of nanomaterials has attracted great attention in recent years. As a possible occupational carcinogen, the genotoxic effects and underlying mechanisms of titanium dioxide nanoparticles (TiO<sub>2</sub> NPs) have been of particular concern. In this study, the effect of TiO<sub>2</sub> NPs (0, 25, 50 and 100 µg/mL) on DNA damage and the role of oxidative stress were investigated using human bronchial epithelial cells (BEAS-2B) as an in vitro model. After detailed characterization, the cytotoxicity of TiO<sub>2</sub> NPs was detected. Through transmission electron microscopy (TEM), we found that TiO<sub>2</sub> NPs entered the cytoplasm but did not penetrate deep into the nucleus of cells. The intracellular levels of reactive oxygen species (ROS) significantly increased in a dose-dependent manner and the ratios of GSH/GSSG also significantly decreased. The results of the normal comet assay were negative, while the Fpg-modified comet assay that specifically detected DNA oxidative damage was positive. Meanwhile, <i>N</i>-acetyl-L-cysteine (NAC) intervention inhibited the oxidative stress and genotoxicity induced by TiO<sub>2</sub> NPs. Therefore, it was suggested that TiO<sub>2</sub> NPs could induce cytotoxicity, oxidative stress and DNA oxidative damage in BEAS-2B cells. DNA oxidative damage may be a more sensitive genetic endpoint to detect the genotoxicity of TiO<sub>2</sub> NPs.
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spelling doaj.art-5f485d87c8ba4863a9f27093bd2ecb0f2023-12-03T12:52:06ZengMDPI AGNanomaterials2079-49912022-07-011215261610.3390/nano12152616DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide NanoparticlesZhangjian Chen0Jiaqi Shi1Yi Zhang2Shuo Han3Jiahe Zhang4Guang Jia5Department of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaDepartment of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaDepartment of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaDepartment of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaDepartment of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaDepartment of Occupational and Environmental Health Sciences, School of Public Health, Peking University, Beijing 100191, ChinaThe genotoxicity of nanomaterials has attracted great attention in recent years. As a possible occupational carcinogen, the genotoxic effects and underlying mechanisms of titanium dioxide nanoparticles (TiO<sub>2</sub> NPs) have been of particular concern. In this study, the effect of TiO<sub>2</sub> NPs (0, 25, 50 and 100 µg/mL) on DNA damage and the role of oxidative stress were investigated using human bronchial epithelial cells (BEAS-2B) as an in vitro model. After detailed characterization, the cytotoxicity of TiO<sub>2</sub> NPs was detected. Through transmission electron microscopy (TEM), we found that TiO<sub>2</sub> NPs entered the cytoplasm but did not penetrate deep into the nucleus of cells. The intracellular levels of reactive oxygen species (ROS) significantly increased in a dose-dependent manner and the ratios of GSH/GSSG also significantly decreased. The results of the normal comet assay were negative, while the Fpg-modified comet assay that specifically detected DNA oxidative damage was positive. Meanwhile, <i>N</i>-acetyl-L-cysteine (NAC) intervention inhibited the oxidative stress and genotoxicity induced by TiO<sub>2</sub> NPs. Therefore, it was suggested that TiO<sub>2</sub> NPs could induce cytotoxicity, oxidative stress and DNA oxidative damage in BEAS-2B cells. DNA oxidative damage may be a more sensitive genetic endpoint to detect the genotoxicity of TiO<sub>2</sub> NPs.https://www.mdpi.com/2079-4991/12/15/2616genotoxicitytitanium dioxide nanoparticlesDNA oxidative damageFpg-modified comet assayoxidative stress
spellingShingle Zhangjian Chen
Jiaqi Shi
Yi Zhang
Shuo Han
Jiahe Zhang
Guang Jia
DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
Nanomaterials
genotoxicity
titanium dioxide nanoparticles
DNA oxidative damage
Fpg-modified comet assay
oxidative stress
title DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
title_full DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
title_fullStr DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
title_full_unstemmed DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
title_short DNA Oxidative Damage as a Sensitive Genetic Endpoint to Detect the Genotoxicity Induced by Titanium Dioxide Nanoparticles
title_sort dna oxidative damage as a sensitive genetic endpoint to detect the genotoxicity induced by titanium dioxide nanoparticles
topic genotoxicity
titanium dioxide nanoparticles
DNA oxidative damage
Fpg-modified comet assay
oxidative stress
url https://www.mdpi.com/2079-4991/12/15/2616
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