In vitro uptake and toxicity studies of metal nanoparticles and metal oxide nanoparticles in human HT29 cells.
Thomas SchneiderMartin WestermannMichael GleiPublished in: Archives of toxicology (2017)
In this paper, we investigated the toxicological behavior of metal nanoparticles (gold, silver) and metal oxide nanoparticles (copper oxide, zinc oxide, titanium dioxide) in vitro in human colorectal adenocarcinoma cells (HT29). We analyzed the cellular uptake by ICP-MS and TEM, the influence on cell viability by MTT assay and trypan blue exclusion test, their effect on DNA damage and/or generation of oxidized bases by alkaline comet assay, and their potential to induce apoptosis by flow cytometry after 24-h nanoparticle treatment with concentrations between 2 and 10 µg/ml. We determined the amount of metal taken up by a single HT29 cell, ranging from 0.02 pg/cell up to 1.39 pg/cell. Cell viability assays showed a significantly decrease for metal oxide nanoparticles using trypan blue exclusion test and for all nanoparticles, except titanium dioxide, using MTT assay. Genotoxic effects after nanoparticle treatment were not observed for the tested concentrations. Apoptosis induction was significantly increased for silver nanoparticles (tested for two sizes) as well as for titanium dioxide and zinc oxide nanoparticles. Our results indicate potential health risks of oral NP uptake by food ingredients or food contamination, making further mechanistic investigations on cellular uptake and toxicity necessary.
Keyphrases
- oxide nanoparticles
- cell cycle arrest
- silver nanoparticles
- induced apoptosis
- dna damage
- oxidative stress
- single cell
- high throughput
- endoplasmic reticulum stress
- endothelial cells
- flow cytometry
- human health
- cell death
- cell therapy
- risk assessment
- squamous cell carcinoma
- multiple sclerosis
- pi k akt
- mesenchymal stem cells
- signaling pathway
- gold nanoparticles
- stem cells
- radiation therapy
- cell proliferation
- drinking water
- health risk
- climate change
- rectal cancer
- ms ms
- dna repair
- high resolution
- pluripotent stem cells
- low density lipoprotein