{"title":"瑞舒伐他汀通过磷脂酰肌醇-3激酶/蛋白激酶B调控间充质干细胞成骨分化","authors":"Xuepeng Wang, Chunchun Zou, Changju Hou, Maoqiang Li, Z. Bian, Liulong Zhu","doi":"10.3760/CMA.J.ISSN.1001-9030.2020.01.029","DOIUrl":null,"url":null,"abstract":"Objective \nTo investigate the effects of rosuvastatin on proliferation, osteogenic differentiation and phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt) expression of mesenchymal stem cells (MSCs). \n \n \nMethods \nMSCs were isolated. Rosuvastatin at concentrations of 1×10-11, 1×10-9 and 1×10-7 mol/L were added to the experimental groups, and dimethylsurfoxide (DMSO) served as control. Cell proliferation was measured by methyl thiazol tetrazolium (MTT) assay. After 3, 7, 14 and 21 days of osteogenic induction, alkaline phosphatase (ALP) quantitative analysis, alizarin red staining and quantitative analysis, real-time quantitative polymerase chain reaction (Real-time PCR) and Western blotting were performed. T-test was used for comparison between two groups, and ANOVA for more than two groups. \n \n \nResults \nAt 24 h and 48 h, the proliferation of MSCs in high concentration group was significantly higher than in the control group (24 h: 3.57±0.24 vs. 3.14±0.14, t=-3.851, P<0.05; 48 h: 4.19±0.18 vs. 3.44±0.11, t=-6.780, P<0.05). Until 72 h, the proliferation with 1×10-9 mol/L rosuvastatin was also significantly increased (5.42±0.13 vs. 4.47±0.16, t=-8.700, P<0.05). At 3rd day after induction culture, 1×10-7 mol/L rosuvastatin significantly enhanced the genes expression of BMP2, Runx 2, OPN 2, OPN and ColⅠ (BMP2: 2.1±0.2 vs. 1.0±0.2, t=-6.736, P<0.05; Runx2: 5.2±0.6 vs. 1.0±0.1, t=-11.959, P<0.05; OPN: 1.8±0.4 vs. 1.0±0.2, t=-3.098, P<0.05; ColⅠ: 1.9±0.3 vs. 1.0±0.3, t=-3.674, P<0.05); 1×10-7 mol/L rosuvastatin could increase the expression of p-Akt/PI3K. The ALP activity after adding 1×10-9 or 1×10-7 mol/L rosuvastatin was significantly increased at 14th and 21st day (14 d: 12.07±1.67, 18.32±2.26 vs. 3.43±0.36, F=7.200, P<0.05; 21 d: 10.74±1.27, 14.71±3.18 vs. 5.76±0.63, F=6.489, P<0.05). The quantitative results of alizarin red were similar to those of the staining. Meanwhile, the quantitative values of alizarin red in the 1×10-9 and 1×10-7 mol/L groups were also significantly increased (14 d: 5.6±0.8, 6.2±1.2 vs. 1.0±0.2, F=5.600, P<0.05; 21 d: 5.8±1.1, 7.1±1.8 vs. 2.4±0.3, F=5.956, P<0.05). \n \n \nConclusion \nRosuvastatin promotes proliferation and osteogenic differentiation of MSCs, which may be related to PI3K/Akt signaling. \n \n \nKey words: \nRosuvastatin; Phosphatidylinositol-3-kinase/protein kinase B signaling pathway; Mesenchymal stem cells; Osteogenic differentiation","PeriodicalId":10065,"journal":{"name":"中华实验外科杂志","volume":"37 1","pages":"101-104"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rosuvastatin regulates osteogenic differentiation of mesenchymal stem cells through phosphatidylinositol-3-kinase/protein kinase B\",\"authors\":\"Xuepeng Wang, Chunchun Zou, Changju Hou, Maoqiang Li, Z. Bian, Liulong Zhu\",\"doi\":\"10.3760/CMA.J.ISSN.1001-9030.2020.01.029\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo investigate the effects of rosuvastatin on proliferation, osteogenic differentiation and phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt) expression of mesenchymal stem cells (MSCs). \\n \\n \\nMethods \\nMSCs were isolated. Rosuvastatin at concentrations of 1×10-11, 1×10-9 and 1×10-7 mol/L were added to the experimental groups, and dimethylsurfoxide (DMSO) served as control. Cell proliferation was measured by methyl thiazol tetrazolium (MTT) assay. After 3, 7, 14 and 21 days of osteogenic induction, alkaline phosphatase (ALP) quantitative analysis, alizarin red staining and quantitative analysis, real-time quantitative polymerase chain reaction (Real-time PCR) and Western blotting were performed. T-test was used for comparison between two groups, and ANOVA for more than two groups. \\n \\n \\nResults \\nAt 24 h and 48 h, the proliferation of MSCs in high concentration group was significantly higher than in the control group (24 h: 3.57±0.24 vs. 3.14±0.14, t=-3.851, P<0.05; 48 h: 4.19±0.18 vs. 3.44±0.11, t=-6.780, P<0.05). Until 72 h, the proliferation with 1×10-9 mol/L rosuvastatin was also significantly increased (5.42±0.13 vs. 4.47±0.16, t=-8.700, P<0.05). At 3rd day after induction culture, 1×10-7 mol/L rosuvastatin significantly enhanced the genes expression of BMP2, Runx 2, OPN 2, OPN and ColⅠ (BMP2: 2.1±0.2 vs. 1.0±0.2, t=-6.736, P<0.05; Runx2: 5.2±0.6 vs. 1.0±0.1, t=-11.959, P<0.05; OPN: 1.8±0.4 vs. 1.0±0.2, t=-3.098, P<0.05; ColⅠ: 1.9±0.3 vs. 1.0±0.3, t=-3.674, P<0.05); 1×10-7 mol/L rosuvastatin could increase the expression of p-Akt/PI3K. The ALP activity after adding 1×10-9 or 1×10-7 mol/L rosuvastatin was significantly increased at 14th and 21st day (14 d: 12.07±1.67, 18.32±2.26 vs. 3.43±0.36, F=7.200, P<0.05; 21 d: 10.74±1.27, 14.71±3.18 vs. 5.76±0.63, F=6.489, P<0.05). The quantitative results of alizarin red were similar to those of the staining. Meanwhile, the quantitative values of alizarin red in the 1×10-9 and 1×10-7 mol/L groups were also significantly increased (14 d: 5.6±0.8, 6.2±1.2 vs. 1.0±0.2, F=5.600, P<0.05; 21 d: 5.8±1.1, 7.1±1.8 vs. 2.4±0.3, F=5.956, P<0.05). \\n \\n \\nConclusion \\nRosuvastatin promotes proliferation and osteogenic differentiation of MSCs, which may be related to PI3K/Akt signaling. \\n \\n \\nKey words: \\nRosuvastatin; Phosphatidylinositol-3-kinase/protein kinase B signaling pathway; Mesenchymal stem cells; Osteogenic differentiation\",\"PeriodicalId\":10065,\"journal\":{\"name\":\"中华实验外科杂志\",\"volume\":\"37 1\",\"pages\":\"101-104\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中华实验外科杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2020.01.029\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华实验外科杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2020.01.029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的探讨瑞舒伐他汀对间充质干细胞(MSCs)增殖、成骨分化及磷脂酰肌醇-3激酶(PI3K)/蛋白激酶B (Akt)表达的影响。方法分离MSCs。实验组分别加入浓度为1×10-11、1×10-9和1×10-7 mol/L的瑞舒伐他汀,对照组分别加入二甲苏福啶(DMSO)。采用甲基噻唑四氮唑(MTT)法检测细胞增殖。成骨诱导3、7、14、21 d后进行碱性磷酸酶(ALP)定量分析、茜素红染色及定量分析、实时定量聚合酶链反应(real-time PCR)和Western blotting。两组间比较采用t检验,两组以上采用方差分析。结果24 h、48 h,高浓度组MSCs的增殖明显高于对照组(24 h: 3.57±0.24 vs. 3.14±0.14,t=-3.851, P<0.05;48 h: 4.19±0.18和3.44±0.11,t = -6.780, P < 0.05)。1×10-9 mol/L瑞舒伐他汀治疗至72 h时,细胞增殖也显著增加(5.42±0.13∶4.47±0.16,t=-8.700, P<0.05)。诱导培养后第3天,1×10-7 mol/L瑞舒伐他汀显著提高BMP2、runx2、opn2、OPN和Col基因表达Ⅰ(BMP2: 2.1±0.2 vs. 1.0±0.2,t=-6.736, P<0.05;Runx2: 5.2±0.6 vs. 1.0±0.1,t=-11.959, P<0.05;OPN: 1.8±0.4 vs. 1.0±0.2,t=-3.098, P<0.05;ColⅠ:1.9±0.3 vs. 1.0±0.3,t=-3.674, P<0.05);1×10-7 mol/L瑞舒伐他汀可增加p-Akt/PI3K的表达。添加1×10-9或1×10-7 mol/L瑞舒伐他汀后第14天和第21天ALP活性显著升高(14 d: 12.07±1.67,18.32±2.26 vs. 3.43±0.36,F=7.200, P<0.05;21 d: 10.74±1.27,14.71±3.18和5.76±0.63,F = 6.489, P < 0.05)。茜素红的定量结果与染色结果相似。同时,1×10-9和1×10-7 mol/L组的芹素红定量值也显著升高(14 d: 5.6±0.8、6.2±1.2 vs. 1.0±0.2,F=5.600, P<0.05;21 d: 5.8±1.1,7.1±1.8和2.4±0.3,F = 5.956, P < 0.05)。结论瑞舒伐他汀促进MSCs增殖和成骨分化,可能与PI3K/Akt信号通路有关。关键词:瑞舒伐他汀;磷脂酰肌醇-3激酶/蛋白激酶B信号通路;间充质干细胞;成骨分化
Rosuvastatin regulates osteogenic differentiation of mesenchymal stem cells through phosphatidylinositol-3-kinase/protein kinase B
Objective
To investigate the effects of rosuvastatin on proliferation, osteogenic differentiation and phosphatidylinositol-3-kinase (PI3K)/protein kinase B (Akt) expression of mesenchymal stem cells (MSCs).
Methods
MSCs were isolated. Rosuvastatin at concentrations of 1×10-11, 1×10-9 and 1×10-7 mol/L were added to the experimental groups, and dimethylsurfoxide (DMSO) served as control. Cell proliferation was measured by methyl thiazol tetrazolium (MTT) assay. After 3, 7, 14 and 21 days of osteogenic induction, alkaline phosphatase (ALP) quantitative analysis, alizarin red staining and quantitative analysis, real-time quantitative polymerase chain reaction (Real-time PCR) and Western blotting were performed. T-test was used for comparison between two groups, and ANOVA for more than two groups.
Results
At 24 h and 48 h, the proliferation of MSCs in high concentration group was significantly higher than in the control group (24 h: 3.57±0.24 vs. 3.14±0.14, t=-3.851, P<0.05; 48 h: 4.19±0.18 vs. 3.44±0.11, t=-6.780, P<0.05). Until 72 h, the proliferation with 1×10-9 mol/L rosuvastatin was also significantly increased (5.42±0.13 vs. 4.47±0.16, t=-8.700, P<0.05). At 3rd day after induction culture, 1×10-7 mol/L rosuvastatin significantly enhanced the genes expression of BMP2, Runx 2, OPN 2, OPN and ColⅠ (BMP2: 2.1±0.2 vs. 1.0±0.2, t=-6.736, P<0.05; Runx2: 5.2±0.6 vs. 1.0±0.1, t=-11.959, P<0.05; OPN: 1.8±0.4 vs. 1.0±0.2, t=-3.098, P<0.05; ColⅠ: 1.9±0.3 vs. 1.0±0.3, t=-3.674, P<0.05); 1×10-7 mol/L rosuvastatin could increase the expression of p-Akt/PI3K. The ALP activity after adding 1×10-9 or 1×10-7 mol/L rosuvastatin was significantly increased at 14th and 21st day (14 d: 12.07±1.67, 18.32±2.26 vs. 3.43±0.36, F=7.200, P<0.05; 21 d: 10.74±1.27, 14.71±3.18 vs. 5.76±0.63, F=6.489, P<0.05). The quantitative results of alizarin red were similar to those of the staining. Meanwhile, the quantitative values of alizarin red in the 1×10-9 and 1×10-7 mol/L groups were also significantly increased (14 d: 5.6±0.8, 6.2±1.2 vs. 1.0±0.2, F=5.600, P<0.05; 21 d: 5.8±1.1, 7.1±1.8 vs. 2.4±0.3, F=5.956, P<0.05).
Conclusion
Rosuvastatin promotes proliferation and osteogenic differentiation of MSCs, which may be related to PI3K/Akt signaling.
Key words:
Rosuvastatin; Phosphatidylinositol-3-kinase/protein kinase B signaling pathway; Mesenchymal stem cells; Osteogenic differentiation