Zip1 转染骨髓间充质干细胞对WNT1/β-catenin信号成骨通路的影响
Effect of Zip1 transfection on WNT1/β-catenin signaling pathway in osteogenic differentiation by bone marrow mesenchymal stem cells
  
DOI:10.3969/j.issn.1006.7108.2018.05.007
中文关键词:  骨髓间充质干细胞,锌转运蛋白1,碱性磷酸酶,骨钙素,成骨分化
英文关键词:BMSCs, ZIP 1, Alkaline phosphatase, Osteocalcin, Osteogenic differentiation
基金项目:广西自然科学基金课题(2015GXNSFAA139136);广西高校青年教师基础能力提升项目(KY2016YB204);广西卫生厅重点课题(S201419-05);国自然科学基金项目(81760796);2017年大学生创新创业训练计划专项经费(省级)(J17143055);中央支持地方高校发展专项资金(04B2017082);广西中医药大学校级科研项目(2015LX027)
作者单位
章晓云1 夏天2* 陈跃平1 廖小林2袁振中2 卓映宏2 冯洋2 蓝佼2 赵斌2 1.广西中医药大学附属瑞康医院创伤骨科与手外科广西 南宁 530011 2.广西中医药大学广西 南宁 530001 
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中文摘要:
      目的 观察ZIP1 siRNA转染的骨髓间充质干细胞对WNT1/β-catenin信号成骨通路的影响。方法 从成年雄性新西兰兔股骨骨髓中提取骨髓间充质干细胞并培养传代,然后使用0.03 mol/L,0.09 mol/L,0.15 mol/L,0.21 mol/L酒精进行培养,经ZIP1 siRNA及ZIP1表达转染后,检测各组骨髓间充质干细胞中ALP、I型胶原、OCN及RUNX2蛋白的表达量。结果 与空白对照组相比,不同酒精组的ALP、I型胶原、OCN及RUNX2蛋白表达量均有所下降,随着浓度升高,其表达量逐渐下降,但0.03mol/L组中ALP及OCN下降不明显,统计学无明显意义(P>0.05),其他各组均有明显的统计学意义(P<0.05),不同酒精组中的I型胶原及RUNX2与正常组之间差异均有明显统计学意义(P<0.05)。与空白对照组对比,ZIP1表达组ALP、I型胶原及OCN表达量明显升高,差异具有明显的统计学意义(P < 0.05),ZIP1siRNA组ALP、OCN表达量明显降低,差异具有明显的统计学意义(P < 0.05),而I型胶原表达量下降不明显,差异无统计学意义(P>0.05);与ZIP1siRNA组相比,ZIP1表达组ALP、I型胶原及OCN表达量明显升高,差异有统计学意义(P < 0.05)。结论 ZIP1能促使骨髓间质干细胞向成骨分化,从而促进骨修复及骨代谢。沉默ZIP1表达能抑制骨髓间充质干细胞的WNT1/β-catenin信号成骨通路的表达,从而抑制促进细胞的成骨分化能力。
英文摘要:
      Objective To study the effect of BMSCs transfected by ZIP1 (Zrt/Irt-like Protein 1) on WNT1/β-catenin signaling pathway in the process of osteogenic differentiation. Methods BMSCs were extracted from bone marrow of the femurs of adult male New Zealand rabbits and cultured under different concentrations of alcohol (0.03 mol/L, 0.09 mol/L, 0.15 mol/L, and 0.21 mol/L, respectively). Cells were transfected by ZIP1 siRNA and ZIP1.The expression ALP, collagen type I, OCN, and RUNX2 were detected in BMSCs. Results Compared with the control group, the protein expression of ALP, collagen type I, OCN, and RUNX2 decreased in different alcohol groups. With the increase of alcohol concentration, the expression decreased gradually. The decrease of ALP and OCN was not significant in 0.03mol/L group (P >0.05). The difference was statistically significant (P<0.05) in other groups. The differences of the expression of collagen type I and RUNX2 between different alcohol groups and normal group were statistically significant (P<0.05). Compared with the control group, the expression of ALP, collagen type I and OCN increased significantly in the ZIP1 group, and the difference was significant (P<0.05). The expression of ALP and OCN, except the type I collagen, decreased significantly in the ZIP1 siRNA group, and the difference was significant (P<0.05). Compared with ZIP1 siRNA group, the expression of ALP, collagen type I, and OCN increased significantly in the ZIP1 group, and the difference was statistically significant (P<0.05). Conclusion ZIP1 promotes the osteogenic differentiation of BMSCs and promotes bone repair and bone metabolism. ZIP1 siRNA suppresses the osteogenic differentiation of BMSCs by activating WNT1/β-catenin signaling pathway.
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