PUBLICATION

Redox Activity and Nano-Bio Interactions Determine the Skin Injury Potential of Co3O4-Based Metal Oxide Nanoparticles toward Zebrafish

Authors
Peng, G., He, Y., Wang, X., Cheng, Y., Zhang, H., Savolainen, K., Mädler, L., Pokhrel, S., Lin, S.
ID
ZDB-PUB-200403-126
Date
2020
Source
ACS nano   14(4): 4166-4177 (Journal)
Registered Authors
Keywords
metal oxide, nano−bio interactions, oxidative stress, redox activity, zebrafish
MeSH Terms
  • Animals
  • Larva
  • Metal Nanoparticles*/toxicity
  • Nanoparticles*
  • Oxidation-Reduction
  • Oxidative Stress
  • Oxides/toxicity
  • Zebrafish
PubMed
32191835 Full text @ ACS Nano
Abstract
Redox-active metal oxide nanoparticles show varying oxidizing capacities and injury potentials toward biological systems. Here, two metal oxide libraries including transition-metal-doped Co3O4 and PdO-Co3O4 with strong chemical contacts were design-synthesized and used to investigate their biological injury potential and mechanisms using zebrafish as a model organism. Among different dopants, Cu significantly increased the oxidizing capacity of Co3O4. An increased amount of PdO resulted in higher density of heterojunctions, which also led to higher oxidizing capacity. The oxidizing capacity of these nanoparticles was positively correlated with higher mortality of dechorionated embryos and severe larval skin injury upon exposure. Using transgenic zebrafish Tg(LysC:eGFP), we show in real time that the redox-active nanoparticles induced skin injury and activated the infiltration of immune cells. Such inflammatory response was confirmed by the increased mRNA expression level of Nrf2a, HO-1, IL-1β, and IL-6 genes. Although the exposure to the nanoparticles alone was not lethal, the skin injury did lower the tolerance level against other environmental contaminants. More importantly, after withdrawing from the nanoparticle exposure, larvae with skin injury could recover within 24 h in uncontaminated medium, indicating such injury was transient and recoverable.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping