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Contact-dependent transfer of TiO2 nanoparticles between mammalian cells
Authors:Julia Schoelermann  Anne Burtey  Zouhir Ekeland Allouni  Hans-Hermann Gerdes
Affiliation:1. Department of Biomedicine, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway and julia.schoelermann@bergenbio.com;3. Department of Biomedicine, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway and;4. Division of Biomaterials, Department of Clinical Dentistry, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway
Abstract:Cellular organelles have been shown to shuttle between cells in co-culture. We hereby show that titanium dioxide (TiO2) nanoparticles (NPs) can be transferred in such a manner, between cells in direct contact, along with endosomes and lysosomes. A co-culture system was employed for this purpose and the NP transfer was observed in mammalian cells including normal rat kidney (NRK) and HeLa cells. We found that the small GTPase Arf6 facilitates the intercellular transfer of smaller NPs and agglomerates. Spherical, anatase nano-TiO2 with sizes of 5 (Ti5) and 40?nm (Ti40) were used in this study. Humans are increasingly exposed to TiO2 NPs from external sources such as constituents of foods, cosmetics, and pharmaceuticals, or from internal sources represented by Ti-based implants, which release NPs upon abrasion. Exposure to 5?mg/l of Ti5 and Ti40 for 24?h did not affect cellular viability but modified their ability to communicate with surrounding cells. Altogether, our results have important implications for the design of nanomedicines, drug delivery and toxicity.
Keywords:ADP ribosylation  cell-to-cell transfer  factor 6 (ARF6)  drug delivery  nanoparticles  titanium dioxide  toxicity
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