Interference between nanoparticles and metal homeostasis

• Published in: Journal of physics. Conference series Vol. 304; no. 1; pp. 012035 - 10
• Main Authors: Petit, A N, Garcia, C Aude, Candéias, S, Casanova, A, Catty, P, Charbonnier, P, Chevallet, M, Collin-Faure, V, Cuillel, M, Douki, T, Herlin-Boime, N, Lelong, C, Luche, S, Mintz, E, Moulis, J M, Nivière, V, Choudens, S Ollagnier de, Rabilloud, T, Ravanat, J L, Sauvaigo, S, Carrière, M, Michaud-Soret, I
• Format: Journal Article
• Language: English
• Published: Bristol IOP Publishing 06.07.2011
• Subjects: Agglomeration; Bacteria; Crystal structure; Crystallinity; E coli; Genotoxicity; Homeostasis; Human; Lipids; Macrophages; Molecular structure; Nanomaterials; Nanoparticles; Perturbation; Physics; Titanium dioxide; Toxicity
• ISSN: 1742-6596; 1742-6588; 1742-6596
• DOI: 10.1088/1742-6596/304/1/012035

The TiO2 nanoparticles (NPs) are now produced abundantly and widely used in a variety of consumer products. Due to the important increase in the production of TiO2-NPs, potential widespread exposure of humans and environment may occur during both the manufacturing process and final use. Therefore, the potential toxicity of TiO2-NPs on human health and environment has attracted particular attention. Unfortunately, the results of the large number of studies on the toxicity of TiO2-NPs differ significantly, mainly due to an incomplete characterization of the used nanomaterials in terms of size, shape and crystalline structure and to their unknown state of agglomeration/aggregation. The purpose of our project entitled NanoBioMet is to investigate if interferences between nanoparticles and metal homeostasis could be observed and to study the toxicity mechanisms of TiO2-NPs with well-characterized physicochemical parameters, using proteomic and molecular approaches. A perturbation of metal homeostasis will be evaluated upon TiO2-NPs exposure which could generate reactive oxygen species (ROS) production. Moreover, oxidative stress consequences such as DNA damage and lipid peroxidation will be studied. The toxicity of TiO2-NPs of different sizes and crystalline structures will be evaluated both in prokaryotic (E. coli) and eukaryotic cells (A549 human pneumocytes, macrophages, and hepatocytes). First results of the project will be presented concerning the dispersion of TiO2-NPs in bacterial medium, proteomic studies on total extracts of macrophages and genotoxicity on pneumocytes.