山东大学学报(医学版) ›› 2017, Vol. 55 ›› Issue (8): 24-29.doi: 10.6040/j.issn.1671-7554.0.2017.059
姬原原1,包景泊2,赵旭1,曹鲁宁1,崔敏1,张娜1,于灵芝1
JI Yuanyuan1, BAO Jingbo2, ZHAO Xu1, CAO Luning1, CUI Min1, ZHANG Na1, YU Lingzhi1
摘要: 目的 探讨白介素17F对大鼠成骨细胞增殖、矿化和Runx2、Osterix表达水平的影响。 方法 分离提取新生24 h内wistar大鼠颅盖骨原代成骨细胞,用含10%胎牛血清的低糖DMEM培养基培养,培养基每3天更换1次。当细胞相互融合生长面积达80%左右时,进行细胞传代。向培养基中加入白介素17F,根据浓度将第4代成骨细胞分为0 ng/mL组(对照组)、1 ng/mL组、10 ng/mL组、20 ng/mL组、50 ng/mL组、100 ng/mL组。分组后继续培养3 d,采用CCK-8试剂盒检测各组成骨细胞增殖率,采用实时荧光定量PCR法和Western blotting法分别检测成骨细胞中Runx2、Osterix的mRNA转录水平和蛋白表达水平。在分组培养第10天,对照组和100 ng/mL组进行矿化结节染色。 结果 20 ng/mL组、50 ng/mL组和100 ng/mL组成骨细胞增殖率较对照组增高(P<0.05),呈浓度依赖性。50 ng/mL组和100 ng/mL组成骨细胞中Runx2、Osterix的mRNA转录水平和蛋白表达水平均高于对照组(P<0.05)。100 ng/mL组成骨细胞矿化结节的染色阳性区域多于对照组。 结论 白介素17F可促进体外培养的大鼠成骨细胞的成骨作用。
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