Toxicity and Metabolomic Impact of Cobalt, Chromium, and Nickel Exposure on HepaRG Hepatocytes.
Marie BellouardMarie GasserSébastien LengletFederica GilardiNasim BararpourMarc AugsburgerAurélien ThomasJean-Claude AlvarezPublished in: Chemical research in toxicology (2022)
Cobalt, chromium, and nickel are used in orthopedic prostheses. They can be released, accumulate in many organs, and be toxic. The aim of this study is to evaluate the cytotoxicity of these metals on human hepatocytes and to improve our knowledge of their cellular toxicity mechanisms by metabolomic analysis. HepaRG cells were incubated for 48 h with increasing concentrations of metals to determine their IC 50 . Then, a nontargeted metabolomic study using liquid chromatography-high-resolution mass spectrometry (LC-HRMS) was done at IC 50 and at a lower concentration (100 nM), near to those found in the blood and liver of patients with prostheses. IC 50 were defined at 940, 2, and 1380 μM for Co, Cr, and Ni, respectively. In vitro , Cr appears to be much more toxic than Co and Ni. Metabolomic analysis revealed the disruption of metabolic pathways from the low concentration of 100 nM, in particular tryptophan metabolism and lipid metabolism illustrated by an increase in phenylacetylglycine, a marker of phospholipidosis, for all three metals. They also appear to be responsible for oxidative stress. Dysregulation of these pathways impacts hepatocyte metabolism and may result in hepatotoxicity. Further investigations on accessible biological matrices should be conducted to correlate our in vitro results with the clinical data of prostheses-bearing patients.
Keyphrases
- high resolution mass spectrometry
- liquid chromatography
- oxidative stress
- mass spectrometry
- ultra high performance liquid chromatography
- metal organic framework
- induced apoptosis
- end stage renal disease
- reduced graphene oxide
- tandem mass spectrometry
- chronic kidney disease
- human health
- gas chromatography
- health risk
- healthcare
- simultaneous determination
- photodynamic therapy
- ejection fraction
- endothelial cells
- carbon nanotubes
- oxide nanoparticles
- single cell
- health risk assessment
- dna damage
- gold nanoparticles
- patient reported outcomes
- fatty acid
- endoplasmic reticulum stress
- cell proliferation
- prognostic factors
- cell death
- heavy metals
- data analysis
- heat stress
- heat shock protein