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MC3T3-E1 Cellular Response and Protein Detection on Surface Potential-Controlled TiO_2 Scale in Serum-Containing Medium

机译:MC3T3-E1细胞反应和蛋白质检测表面电位控制的TiO_2在含血清培养基中的规模

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MC3T3-E1 cell differentiation and related surface potentials of rutile-type TiO_2 scales formed on Ti are controlled by varying the Ti heat treatment conditions in a N_2 atmosphere containing a trace amount of O_2. The zeta potentials of the samples heated at 873 and 973 K for 1 h show large negative and positive values, respectively, while cell differentiation on the surface is enhanced in both cases (14 days incubation). In the case of untreated Ti, the cell differentiation diminishes and the zeta potential becomes more neutral. Protein detection by an immunogold-labeling technique and Ca and P detection by time-of-flight secondary ion mass spectrometry reveal that both an adhesive protein such as fibronectin and non-adhesive protein such as albumin adsorbed on the scales formed in 1 h at 873 and 973 K, respectively. And then, the Ca and P were also detected on the charged scales. In the case of untreated Ti, both fibronectin and albumin adsorbed, but no Ca and P were detected. The present findings illuminate the relationship between charged surfaces and MC3T3-E1 cellular response.
机译:通过在含有痕量O_2的N_2气氛中改变Ti热处理条件,控制在Ti上形成的金红石型TiO_2刻度的MC3T3-E1细胞分化和相关表面电位。在873和973k中加热的样品的ζ电位分别显示出大的阴性和正值,而在两种情况下,表面的细胞分化会增强(孵育14天)。在未经处理的Ti的情况下,细胞分化会降低,并且ζ电位变得更加中性。通过免疫角质标记技术和Ca和P检测通过飞行时间二次离子质谱法检测蛋白质检测,揭示了粘合剂蛋白,如纤维素和非粘合剂蛋白如白蛋白,在873处形成1小时内形成的鳞片中形成的鳞片分别为973 k。然后,在充电的尺度上也检测到CA和P.在未处理的Ti的情况下,检测到纤连蛋白和白蛋白,但没有检测到Ca和P。本研究结果照亮了带电表面和MC3T3-E1细胞反应之间的关系。

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