Abstract
In an effort to examine signaling pathway of inflammation of the mouse liver caused by intragastric administration of titanium dioxide nanoparticles (NPs), we assessed Toll‐like receptor‐2 (TLR2), TLR‐4, IκB kinase (IKK‐α, IKK‐β), IκB nucleic factor‐κB (NF‐κB), NF‐κBP52, NF‐κBP65, tumor necrosis factor‐α (TNF‐α), NF‐κB‐inducible kinase (NIK), interleukin‐2 (IL‐2), biochemical parameters of liver functions, and histopathological changes and liver ultrastructure in the TiO~2~ NPs‐treated mice. The results showed the titanium accumulation in liver, histopathological changes and hepatocytes apoptosis of mice liver, and the liver function damaged by TiO~2~ NPs. The real‐time quantitative reverse transcriptase polymerase chain reaction and enzyme‐linked immunosorbent assay analyses showed that TiO~2~ NPs can significantly increase the mRNA and protein expression of TLR2 and TLR4 and several inflammatory cytokines, including IKK1, IKK2, NF‐κB, NF‐κBP52, NF‐κBP65, TNF‐α, and NIK, and TiO~2~ NPs can significantly decrease the mRNA and protein expression of IκB and IL‐2. The results of this study added to our understanding of TiO~2~ NPs‐induced liver toxicity. It implied that the signaling pathway of liver injury in the TiO~2~ NPs‐stimulated mouse liver sequentially might occur via activation of TLRs→NIK→IκB kinase→NF‐κB→TNF‐α→inflammation→apoptosis→liver injury. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2010.