骨化三醇通过PI3K/AKT促进BMP9诱导的间充质干细胞成骨分化作用
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国家自然科学基金项目(81101360),上海市科委自然基金项目(16ZR1422000),教育部归国留学人员启动基金(20134701),上海交通大学医工交叉基金(YG2015MS67)


Calcitriol Promotes BMP9 Induced Mesenchymal Stem Cells Osteogenesis Through PI3K/AKT Signaling Pathway
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    摘要:

    目的 研究骨化三醇(calcitriol)对骨形态发生蛋白9(bone morphogenetic protein 9,BMP9)诱导的间充质干细胞(mesenchymal stem cells,MSCs)成骨分化作用的影响。方法 实验分为4组:对照组、calcitriol组、BMP9组、calcitriol联合BMP9组。通过PNPP 法检测各组碱性磷酸酶(alkaline phosphatase,ALP)活性;通过RT-PCR和Western blotting方法检测成骨分化标记物骨钙蛋白(osteocalcin,OCN)和骨桥蛋白(osteopontin,OPN)表达变化,同时检测AKT和β-catenin磷酸化水平以及和ALP活性水平;茜素红染色检测矿化结节形成。此外,用原子力显微镜测试MSCs成骨分化过程中细胞形态及细胞弹性模量改变。结果 calcitriol单独作用对MSCs成骨分化过程无明显作用,但是calcitriol可以增强BMP9诱导MSCs的ALP、OCN、OPN表达和矿化结节形成。同时,calcitriol和BMP9作用均不影响细胞弹性模量数值。BMP9 和calcitriol联合作用可以增强AKT和β-catenin磷酸化水平,而PI3K抑制剂应用以后可以抑制这种磷酸化变化,并抑制联合作用后的ALP活性。calcitriol作用以后不影响BMP9诱导的BMP/Smad信号通路。结论 calcitriol通过激活PI3K/AKT信号通路从而协同BMP9 促进MSCs成骨分化。研究不同调控因子对MSCs成骨分化的作用及机制对于骨质疏松等疾病的治疗和骨组织工程的发展有一定意义。

    Abstract:

    Objective To investigate the effect of calcitriol on osteogenic differentiation of mesenchymal stem cells (MSCs) induced by bone morphogenetic protein 9 (BMP9). Methods The experiment was divided into four groups: control group, calcitriol group, BMP9 group and BMP9+calcitriol group. Quantitative PNPP method was used to detect alkaline phosphatase (ALP) activity. RT-PCR and Western blotting method analyzed expression of osteocalcin(OCN)and osteopontin (OPN). Alizarin red staining assessed the formation of mineralized nodules. In addition, the changes of cell morphology and elastic modulus during osteogenic differentiation were studied by atomic force microscope. ResultsCompared with control group, calcitriol alone had no significant effect on the osteogenic differentiation of MSCs, but calcitriol could enhanced expression of osteogenic markers and formation of mineralized nodules induced by BMP9. However, neither calcitriol nor BMP9 could affect elastic modulus of cells. The combined treatment of BMP9 and calcitol could enhance phosphorylation of AKT and β-catenin which were both important for osteogenesis. The pretreated PI3K inhibitor could inhibit phosphorylation of AKT and β-catenin as well as ALP activity in BMP9+calcitriol group. In addition, calcitriol did not affect the BMP/Smad signaling pathway induced by BMP9. Conclusions Calcitriol synergies with BMP9 could promote MSCs osteogenesis by activating the PI3K/AKT signaling pathway. The study about effects and mechanisms of different regulatory factors on osteogenic differentiation of MSCs is of great significance for the treatment of osteoporosis and the development of bone tissue engineering.

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陈晓婷,姜天缘,夏超,胡燕,周妍,高艳虹.骨化三醇通过PI3K/AKT促进BMP9诱导的间充质干细胞成骨分化作用[J].医用生物力学,2019,34(2):200-206

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  • 收稿日期:2018-05-14
  • 最后修改日期:2018-07-01
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  • 在线发布日期: 2019-04-23
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