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刘 艳, 胡 赟, 张 夏, 等.双磷酸盐对高糖环境下BMSCs自噬相关因子Beclin1和LC3Ⅱ影响的研究.四川大学学报(医学版),2018,49(5):694-699
双磷酸盐对高糖环境下BMSCs自噬相关因子Beclin1和LC3Ⅱ影响的研究
Effects of Bisphosphonates on Beclin1 and LC3Ⅱ Induced by High-glucose in Rat Bone Marrow Mesenchymal Stem Cells
  
中文关键词:  自噬 双磷酸盐 糖尿病性骨质疏松
英文关键词:Autophagy Bisphosphonates Diabetic osteoporosis
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中文摘要:
      目的 研究双磷酸盐对高糖环境下骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs)自噬相关因子Beclin1和微管相关蛋白1轻链3(microtubule-associated protein 1 light chain 3, LC3)Ⅱ的影响。 方法 BMSCs体外分离与培养,进行成骨、成软骨及成脂三向分化诱导与鉴定,配置含浓度梯度10-6~10-9mmol/L双磷酸盐的高糖(30 mmol/L)培养基,采用CCK-8检测BMSCs的增殖活性后选定用于实验的双磷酸盐浓度为10-9 mmol/L。另取BMSCs分为3组:正常对照组(D-葡萄糖5.6 mmol/L),高糖组(D-葡萄糖30 mmol/L),高糖(D-葡萄糖30 mmol/L)+双磷酸盐(10-9 mmol/L)组。用real time -PCR检测3组细胞LC3和Beclin1的基因表达,Western blot检测3组细胞LC3Ⅱ和Beclin1蛋白的表达水平,透射电镜观察自噬体。 结果 鉴定结果示所得BMSCs具有成骨、成软骨及成脂分化能力。高糖组LC3和Beclin1 mRNA、LC3Ⅱ和Beclin1蛋白的表达较正常对照组增高(P<0.01),而高糖组+双磷酸盐组较高糖组低(P<0.05);透射电镜显示高糖组细胞中自噬体数量最多,高糖+双磷酸盐组其次,正常对照组最少。 结论 高糖环境下BMSCs自噬水平升高,而双磷酸盐能下调高糖环境下BMSCs自噬相关因子Beclin1和LC3Ⅱ的表达。
英文摘要:
      Objective To investigate the effects of bisphosphonates on autophagy induced by high-glucose in rat bone marrow mesenchymal stem cells (BMSCs). Methods BMSCs were isolated and cultured in vitro,identified by undergoing osteogenic/chondrogenic/adipogenic differentiation, the concentration of bisphosphonates was determined by CCK-8 method. The cells were cultured in normal glucose (5.6 mmol/L D-glucose), high glucose (30 mmol/L D-glucose), and high glucose with bisphosphonates (30 mmol/L D-glucose+10-9 mmol/L bisphosphonates). At 48 h, mRNA expression levels of autophagy related genes Beclin1 and microtubule-associated protein 1 light chain 3 (LC3) were dected by real-time PCR, protein expression levels of Beclin1 and LC3Ⅱ were detected by Western blot, and the autophagy body was observed by transmission electron microscopy (TEM). Results The results showed that BMSCs had the ability of osteogenenic, chondrogenic and adipogenic differentiation. Compared with the control group and high glucose with bisphosphonates group, the mRNA expressions of Beclin1 and LC3 and protein expressions of Beclin1 and LC3Ⅱ in the high glucose group were increased (P<0.01 or P<0.05). TEM showed that the number of autophagy body in high glucose group was higher than that in normal group and high glucose with bisphosphonates group. Conclusion Bisphosphonates may play a role of down-regulating the expression of Beclin1 and LC3Ⅱ induced by high-glucose in BMSCs.
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