TY - JOUR T1 - Type of Cell Death Induced by Seven Metals in Cultured Mouse Osteoblastic Cells JF - In Vivo JO - In Vivo SP - 507 LP - 512 VL - 24 IS - 4 AU - RENÉ GARCÍA CONTRERAS AU - JOSÉ ROGELIO SCOUGALL VILCHIS AU - HIROSHI SAKAGAMI AU - YUKO NAKAMURA AU - YUKIO NAKAMURA AU - YASUSHI HIBINO AU - HIROSHI NAKAJIMA AU - JUN SHIMADA Y1 - 2010/07/01 UR - http://iv.iiarjournals.org/content/24/4/507.abstract N2 - The use of dental metal alloys in the daily clinic makes it necessary to evaluate the cytotoxicity of eluted metal components against oral cells. However, the cytotoxic mechanism and the type of cell death induced by dental metals in osteoblasts have not been well characterized. This study investigated the cytotoxicity of seven metals against the mouse osteoblastic cell line MC3T3-E1. α-MEM was used as a culture medium, since this medium provided much superior proliferation of MC3T3-E1 cells over DMEM. Ag (NH3)2F was the most cytotoxic, followed by CuCl>CuCl2 >CoCl2, NiCl2>FeCl3 and FeCl2 (least toxic). None of the metals showed any apparent growth stimulating effect (so-called ‘hormesis’) at lower concentrations. A time course study demonstrated that two hours of contact between oral cells and Ag (NH3)2F, CuCl, CoCl2 or NiCl2 induced irreversible cell death. Contact with these metals induced a smear pattern of DNA fragmentation without activation of caspase-3. Preincubation of MC3T3-E1 cells with either a caspase inhibitor (Z-VAD-FMK) or autophagy inhibitors (3-methyladenine, bafilomycin) failed to rescue them from metal cytotoxicity. These data suggest the induction of necrotic cell death rather than apoptosis and autophagy by metals in this osteoblastic cell line. ER -