Toxicity of TiO Nanoparticles: Validation of Alternative Models.

Fiche publication

Date publication

juillet 2020

Journal

International journal of molecular sciences

Auteurs

Membres identifiés du Cancéropôle Est :
Pr SCHNEIDER Raphaël , Dr BONNET Céline , Pr RIHN Bertrand

Tous les auteurs :
Leroux MM, Doumandji Z, Chézeau L, Gaté L, Nahle S, Hocquel R, Zhernovkov V, Migot S, Ghanbaja J, Bonnet C, Schneider R, Rihn BH, Ferrari L, Joubert O

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/32659965

Résumé

There are many studies concerning titanium dioxide (TiO) nanoparticles (NP) toxicity. Nevertheless, there are few publications comparing and exposure, and even less comparing air-liquid interface exposure (ALI) with other and exposures. The identification and validation of common markers under different exposure conditions are relevant for the development of smart and quick nanotoxicity tests. In this work, cell viability was assessed by WST-1 and LDH assays after the exposure of NR8383 cells to TiO NP sample. To evaluate gene expression profile, NR8383 cells were exposed to TiO NP during 4 h at 3 cm of TiO NP/cm of cells or 19 μg/mL, in two settings-submerged cultures and ALI. For the study, Fischer 344 rats were exposed by inhalation to a nanostructured aerosol at a concentration of 10 mg/m, 6 h/day, 5 days/week for 4 weeks. This was followed immediately by gene expression analysis. The results showed a low cytotoxic potential of TiO NP on NR8383 cells. Despite the absence of toxicity at the doses studied, the different exposures to TiO NP induce 18 common differentially expressed genes (DEG) which are involved in mitosis regulation, cell proliferation and apoptosis and inflammation transport of membrane proteins. Among these genes, we noticed the upregulation of , , and genes which could be suggested as early response biomarkers after exposure to TiO NP. On the other hand, the comparison of the three models helped us to validate the alternative ones, namely submerged and ALI approaches.