文摘
Silicon (Si) incorporated porous TiO2 coating (Si-TiO2) prepared on titanium (Ti) by micro-arc oxidation (MAO) technique was demonstrated to be cytocompatible in previous studies. In view of the potential clinical applications, a detailed in vitro study of the biological activity of Si-TiO2 coating, in terms of osteoblast (MC3T3-E1 cells) morphology, proliferation, differentiation and mineralization was performed. Immunofluo-rescent staining indicated that cells seeded on the Si-TiO2 coating showed improved adhesion with developing mature cytoskeletons, which contained numerous distinct and well-defined actin stress fibers in the cell membranes compared with those on the TiO2 coating and Ti plate. Results from proliferation assay showed that the proliferation rate of cells seeded on the Si-TiO2coating was significantly faster than that on the TiO2 coating and Ti plate. Furthermore, the analysis of osteogenic gene expression demonstrated that the Si-TiO2 coating stimulated the expression of osteoblast-related genes and promoted differentiation and mineralization of MC3T3-E1 cells. In addition, the Si-TiO2 coating differentially regulated Wnt signaling pathway by up-regulating the expression of low-density lipoprotein (LDL) receptor-related protein 5 (Lrp5), and down-regulating the expression of Dickkopf-1 (Dkkl). All together, these results indicate that the investigated titanium with Si-TiO2 coating is biocompatible and a good candidate material used as implants.