PUBLICATION
Mechanism of toxic effects of Nano-ZnO on cell cycle of zebrafish (Danio rerio)
- Authors
- Hou, J., Liu, H., Zhang, S., Liu, X., Hayat, T., Alsaedi, A., Wang, X.
- ID
- ZDB-PUB-190513-7
- Date
- 2019
- Source
- Chemosphere 229: 206-213 (Journal)
- Registered Authors
- Keywords
- Cell cycle, Cyclins, DNA replication, Nano-ZnO, Toxicity
- MeSH Terms
-
- Animals
- Cell Cycle/drug effects*
- Cell Differentiation/drug effects
- Cell Division/drug effects
- Cell Proliferation/drug effects
- Nanostructures/toxicity*
- Zebrafish*
- Zinc Oxide/chemistry*
- Zinc Oxide/toxicity*
- PubMed
- 31078877 Full text @ Chemosphere
Citation
Hou, J., Liu, H., Zhang, S., Liu, X., Hayat, T., Alsaedi, A., Wang, X. (2019) Mechanism of toxic effects of Nano-ZnO on cell cycle of zebrafish (Danio rerio). Chemosphere. 229:206-213.
Abstract
The release of nano-zinc oxide (nano-ZnO) into the environment may lead to unpredictable risks, thus it is necessary to study its potential harm to organisms. In this study, zebrafish exposed to nano-ZnO were analyzed through cDNA microarrays to provide insight into the toxic effect of nano-ZnO on aquatic organisms at the molecular level. Results found that nano-ZnO inhibited the normal growth and development of zebrafish and other life activities by affecting the process of cell cycle. The nano-ZnO inhibited the expression of the cyclins (Cycs), cyclin-dependent kinases (CDK) and the minichromosome maintenance (MCM), making the activation of Cyc/CDK complexs (CycD/CDK4, 6; CycE/CDK2; CycA/CDK2) and MCM fail and resulting in DNA replication disorder in different periods (G1, M and G2 phase). Therefore, the normal activities of individual organism such as cell division, differentiation and proliferation and the functions of DNA binding and intracellular transfer were disturbed. These findings contribute to our understanding of the toxicity of ZnO NPs to aquatic organisms, and also provide an evaluation basis for assessing the environmental impact of nano materials.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping