Silica coated iron oxide nanoparticles-induced cytotoxicity, genotoxicity and its underlying mechanism in human HK-2 renal proximal tubule epithelial cells
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31326033
DOI
10.1016/j.mrgentox.2019.05.015
PII: S1383-5718(18)30428-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cytotoxicity, DNA damage, Kidneys, Magnetic nanoparticles, ROS,
- MeSH
- apoptóza účinky léků MeSH
- buněčné linie MeSH
- buněčný cyklus účinky léků MeSH
- dvouřetězcové zlomy DNA MeSH
- epitelové buňky účinky léků MeSH
- geny p53 MeSH
- histony genetika MeSH
- lidé MeSH
- magnetické nanočástice toxicita MeSH
- mikrotubuly účinky léků MeSH
- oxid křemičitý toxicita MeSH
- oxid železnato-železitý toxicita MeSH
- poškození DNA * MeSH
- povrchové vlastnosti MeSH
- proximální tubuly ledvin cytologie MeSH
- reaktivní formy kyslíku MeSH
- testy genotoxicity MeSH
- virová transformace buněk MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- H2AX protein, human MeSH Prohlížeč
- histony MeSH
- magnetické nanočástice MeSH
- oxid křemičitý MeSH
- oxid železnato-železitý MeSH
- reaktivní formy kyslíku MeSH
Iron oxide nanoparticles (IONPs) have a great potential with regard to cell labelling, cell tracking, cell separation, magnetic resonance imaging, magnetic hyperthermia, targeted drug and gene delivery. However, a growing body of research has raised concerns about the possible unwanted adverse cytotoxic effects of IONPs. In the present study, the in vitro cellular uptake, antiproliferative activity, cytotoxicity, genotoxicity, prooxidant, microtubule-disrupting and apoptosis-inducing effect of Fe3O4@SiO2 and passivated Fe3O4@SiO2-NH2 nanoparticles on human renal proximal tubule epithelial cells (HK-2) have been studied. Both investigated silica coated IONPs were found to have cell growth-inhibitory activity in a time- and dose-dependent manner. Determination of cell cycle phase distribution by flow cytometry demonstrated a G1 and G2/M phase accumulation of HK-2 cells. A tetrazolium salt cytotoxicity assay at 24 h following treatment demonstrated that cell viability was reduced in a dose-dependent manner. Microscopy observations showed that both Fe3O4@SiO2 and Fe3O4@SiO2-NH2 nanoparticles accumulated in cells and appeared to have microtubule-disrupting activity. Our study also revealed that short term 1 h exposure to 25 and 100 μg/mL of silica coated IONPs causes genotoxicity. Compared with vehicle control cells, a significantly higher amount of γH2AX foci correlating with an increase in DNA double-strand breaks was observed in Fe3O4@SiO2 and Fe3O4@SiO2-NH2-treated and immunestained HK-2 cells. The investigated nanoparticles did not trigger significant ROS generation and apoptosis-mediated cell death. In conclusion, these findings provide new insights into the cytotoxicity of silica coated IONPs that may support their further safer use.
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