文章摘要
周骅 曹新生 胡泽兵 王瀚 王艺璇 张舒.模拟微重力通过调节AKT 磷酸化抑制前成骨细胞的增殖[J].,2017,17(2):229-232
模拟微重力通过调节AKT 磷酸化抑制前成骨细胞的增殖
Simulated Microgravity Inhibits the Proliferation of Osteoblasts byRegulating the Phosphorylation of AKT
  
DOI:
中文关键词: 模拟微重力  MC3T3-E1 细胞  AKT  增殖
英文关键词: Simulated microgravity  MC3T3-E1 cell  AKT  Cell proliferation
基金项目:国家自然科学基金项目(31570939;81471815;31170889)
作者单位
周骅 曹新生 胡泽兵 王瀚 王艺璇 张舒 第四军医大学航空航天生物动力学教研室 
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中文摘要:
      目的:研究模拟微重力对前成骨细胞的增殖作用及其分子机制。方法:利用2D 回转器模拟失重条件培养前成骨细胞 MC3T3-E1 24 小时;将p-AKT 激活剂SC79 加入细胞培养基后模拟失重条件下培养前成骨细胞MC3T3-E1 24 小时;利用 Western blot技术分别检测细胞增殖相关蛋白PCNA以及AKT、p-AKT 的表达变化情况。结果:①与对照组相比,模拟失重组前成 骨细胞增殖受到抑制(P<0.01),p-AKT/AKT 比值减小(P<0.01);②加入SC79 组与对照组相比,p-AKT/AKT 比值显著增加;③加 入SC79 的模拟失重组(MG+SC79)与模拟失重组相比(MG),p-AKT/AKT 比值增加,PCNA 蛋白表达增加(P<0.01),成骨细胞增 殖有所恢复。结论:模拟微重力可能通过抑制AKT 的磷酸化形式抑制前成骨细胞的增殖,加入p-AKT 激活剂可部分恢复前成骨 细胞的增殖。
英文摘要:
      Objective:To investigate the effect of simulated microgravity on the proliferation and the molecular mechanism of the osteoblast.Methods:2D rotator was used to simulate weightlessness condition. The MC3T3-E1 cells were divided into 4 groups: control group (CON), the simulated weightlessness group (MG), the control with SC79 group (CON+SC79) and simulated weightlessness treatment with SC79 group (MG+SC79). AKT phosphorylation activator SC79 was added into the cell culture medium before exposing to simulated weightlessness, then all the MC3T3-E1 cells were cultured for 24 h. Changes among MC3T3-E1 cells were detected by Western blot analysis, which including cell proliferation related protein PCNA, p-AKT and AKT.Results:① Compared with the CON group, cell proliferation of MG group is inhibited (P<0.01), and the ratio of p-AKT/AKT was decreased (P<0.01).② Compared with the CON group, the ratio of p-AKT/AKT of CON+SC79 group was raised. ③Compared with MG group, p-AKT / AKT ratio was increased, PCNA protein expression was increased partially (P <0.01), and osteoblast proliferation had been restored in the MG+SC79 group.Conclusion:Simulated microgravity can inhibit the proliferation of osteoblasts by inhibiting the phosphorylation of AKT. The proliferation of osteoblasts are partially restored by the addition of p-AKT activator.
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