Wnt3a对人骨髓间充质干细胞成骨分化的影响及机制研究  被引量:8

Effect and Mechanism of Wnt3a on Osteogenic Differentiation of Human Bone Marrow Mesenchymal Stem Cells

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作  者:赵芳英 高秀秋 刘姊凤 ZHAO Fangying,GAO Xiuqiu,LIU Zifeng(Department of Endodontics, The Second Affiliated Hospital, Jinzhou Medical University,Jinzhou 121000,Chin)

机构地区:[1]锦州医科大学附属第二医院牙体牙髓科,辽宁锦州121000

出  处:《中国医科大学学报》2018年第7期617-621,共5页Journal of China Medical University

基  金:辽宁省科学事业公益研究基金(2015001014)

摘  要:目的探讨Wnt3a对人骨髓间充质干细胞成骨分化及Wnt/β-catenin信号通路的影响。方法采用成骨诱导培养基联合Wnt3a蛋白(10ng/m L)诱导人骨髓间充质干细胞分化,通过镜下形态学和茜素红染色评价成骨分化水平。采用实时PCR及Western blotting法检测Wnt3a干预下骨髓间充质干细胞分化过程中第1、5、10、15和20天RUNX2、β-catenin及BSP的表达情况。结果Wnt3a干预下充质干细胞向成骨细胞分化程度明显高于对照组。Wnt3a能提高RUNX2、β-catenin及BSP mRNA和蛋白的表达水平(P<0.05),表达于干预第10天时达到高峰,随后呈轻度下降趋势。结论 Wnt3a通过激活Wnt/β-catenin信号通路调控人骨髓间充质干细胞成骨分化。Objective To investigate the effect of Wnt3a on the osteogenic differentiation of human bone marrow mesenchymal stem cells and the Wnt/β-catenin signaling pathway. Methods We induced the differentiation of human bone marrow mesenchymal stem cells using an osteogenic induction medium supplemented with the Wnt3a protein(10ng/m L) to evaluate its osteogenic differentiation by microscopic morphology and alizarin red staining. Real-time PCR and Western blotting were used to detect the expression of Runt-related transcription factor 2(RUNX2),β-catenin,and bone sialoprotein(BSP) on day 1,5,10,15,and 20 after treatment with Wnt3a. Results Mesenchymal stem cell differentiation into osteoblasts was significantly increased by Wnt3a compared with that of the control group. Moreover,Wnt3a increased the expression of RUNX2,β-catenin,and BSP(P〈0.05),levels of which reached a peak at day 10 after treatment with Wnt3a. Conclusion Wnt3a participated in and regulated the osteogenic differentiation of human bone marrow mesenchymal stem cells by activating the Wnt/β-catenin signaling pathway.

关 键 词:人骨髓间充质干细胞 成骨分化 WNT3A Β-CATENIN RUNX2 BSP 

分 类 号:R780.2[医药卫生—口腔医学]

 

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