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Zinc oxide nanoparticles exhibit cytotoxicity and genotoxicity through oxidative stress responses in human lung fibroblasts and Drosophila melanogaster

Authors Ng CT, Yong LQ, Hande MP, Ong CN, Yu LE, Bay BH, Baeg GH

Received 11 October 2016

Accepted for publication 3 December 2016

Published 28 February 2017 Volume 2017:12 Pages 1621—1637

DOI https://doi.org/10.2147/IJN.S124403

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Cristian Vilos

Peer reviewer comments 3

Editor who approved publication: Dr Thomas J Webster

Cheng Teng Ng,1,2,* Liang Qing Yong,1,* Manoor Prakash Hande,3 Choon Nam Ong,2 Liya E Yu,4 Boon Huat Bay,1 Gyeong Hun Baeg1

1Department of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; 2Environmental Research Institute, National University of Singapore, Singapore; 3Department of Physiology, Yong Loo Lin School of Medicine, 4Department of Civil and Environmental Engineering, National University of Singapore, Singapore, Singapore

*These authors contributed equally to this work

Background: Although zinc oxide nanoparticles (ZnO NPs) have been widely used, there has been an increasing number of reports on the toxicity of ZnO NPs. However, study on the underlying mechanisms under in vivo conditions is insufficient.
Methods: In this study, we investigated the toxicological profiles of ZnO NPs in MRC5 human lung fibroblasts in vitro and in an in vivo model using the fruit fly Drosophila melanogaster. A comprehensive study was conducted to evaluate the uptake, cytotoxicity, reactive oxygen species (ROS) formation, gene expression profiling and genotoxicity induced by ZnO NPs.
Results: For in vitro toxicity, the results showed that there was a significant release of extracellular lactate dehydrogenase and decreased cell viability in ZnO NP-treated MRC5 lung cells, indicating cellular damage and cytotoxicity. Generation of ROS was observed to be related to significant expression of DNA Damage Inducible Transcript (DDIT3) and endoplasmic reticulum (ER) to nucleus signaling 1 (ERN1) genes, which are ER stress-related genes. Oxidative stress induced DNA damage was further verified by a significant release of DNA oxidation product, 8-hydroxydeoxyguanosine (8-OHdG), as well as by the Comet assay. For the in vivo study using the fruit fly D. melanogaster as a model, significant toxicity was observed in F1 progenies upon ingestion of ZnO NPs. ZnO NPs induced significant decrease in the egg-to-adult viability of the flies. We further showed that the decreased viability is closely associated with ROS induction by ZnO NPs. Removal of one copy of the D. melanogaster Nrf2 alleles further decreased the ZnO NPs-induced lethality due to increased production of ROS, indicating that nuclear factor E2-related factor 2 (Nrf2) plays important role in ZnO NPs-mediated ROS production.
Conclusion: The present study suggests that ZnO NPs induced significant oxidative stress-related cytotoxicity and genotoxicity in human lung fibroblasts in vitro and in D. melanogaster in vivo. More extensive studies would be needed to verify the safety issues related to increased usage of ZnO NPs by consumers.

Keywords: zinc oxide nanoparticles, ROS, oxidative stress, MRC5 cells, Drosophila
 

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