作者: Bernhard Setzer , Maria Bächle , Marc C. Metzger , Ralf J. Kohal
DOI: 10.1016/J.BIOMATERIALS.2008.10.054
关键词: Analytical chemistry 、 Cytoskeleton organization 、 Cubic zirconia 、 Materials science 、 Integrin 、 Cellular differentiation 、 Bone morphogenetic protein 7 、 Scanning electron microscope 、 Biophysics 、 RUNX2 、 Titanium
摘要: Abstract The osteoblastic cell-line hFOB 1.19 with the potential to proliferate and differentiate revealed that cellular differentiation is not affected by material roughness on newly developed zirconia implant materials. Materials under investigation were surfaces machined titanium (Ti-m), modified (TiUnite ® ), (TZP-A-m), (ZiUnite alumina-toughened (ATZ-m) (ATZ-mod). After surface description scanning electron microscopy (SEM) atomic force (AFM), proliferation (EZ4U, Casy1) examined after days 1, 3, 7, 14, 21, 28. Osteogenic was visualized alkaline phosphatase staining, mineralization assay (alizarin red) expression analysis (RT-PCR) of bone- extracellular matrix-related genes. Proliferation rough reduced both zirconia. Cell-attachment cytoskeleton organization documented confocal laser (CLSM) elucidated attenuated cell attachment within first 4 h be reason for impaired proliferation. A specific up-regulation m-RNAs in an early event (RUNX2, NELL-1, RUNX3, BMP7) a late (Integrin B3) could observed TiUnite ZiUnite . For IBSP Integrin B1 described at day 21. In total, neither nor roughness.