Wu Zhe, Zhang Jiadi, Gu Xu, Zhang Xiaoxiao, Shi Shuman, Liu Chang
Key Laboratory of Oral Medicine, Guangzhou Institute of Oral Disease, Stomatology Hospital of Guangzhou Medical UniversityGuangzhou 510140, China; Department of Prothodontics, School of Stomatology, Jilin UniversityChangchun 130021, China.
Department of Prothodontics, School of Stomatology, Jilin University Changchun 130021, China.
Am J Transl Res. 2016 Jul 15;8(7):3032-40. eCollection 2016.
The balance of osteogenesis and adipogenesis in bone marrow mesenchymal stem cells (BMSCs) is disrupted in osteoporosis. This study was designed to investigate the effects of extract of Ginkgo biloba (EGB) on proliferation, osteogenic and adipogenic differentiation of bone marrow mesenchymal stem cells in vitro. The effect of EGB on proliferation was evaluated by CCK-8 assay and flow cytometry. Osteogenic differentiation was evaluated by Alizarin Red S staining and Alkaline phosphatase assay. Adipogenic differentiation was evaluated by Oil Red O staining. Quantitative real-time polymerase chain reaction (Real-time PCR) was used to detect the expression of osteogenic specific genes (BMP-2, Runx2 and Colla1) and adipogenic specific genes (ap2, PPARγ). EGB did not significantly affect proliferation of BMSCs. However, it increased the calcium accumulation and significantly promoted the activity of alkaline phosphatase, especially when the concentration of EGB reached 150 µg/mL. EGB dose-dependently inhibited the adipogenic ability of BMSCs. The osteogenic-related genes (BMP-2, Runx2, Colla1) were overexpressed while the expression of genes involved in adipogenesis, such as PPAR-γ and ap2, was decreasing with the increase of EGB concentration. Our data proves that EGB inhibited adipocyte differentiation and enhanced osteogenic differentiation in BMSCs, but had no effect on the proliferation of BMSCs.
骨质疏松症中,骨髓间充质干细胞(BMSCs)的成骨与成脂平衡被打破。本研究旨在探讨银杏叶提取物(EGB)对体外培养的骨髓间充质干细胞增殖、成骨及成脂分化的影响。采用CCK-8法和流式细胞术评估EGB对细胞增殖的影响。通过茜素红S染色和碱性磷酸酶检测评估成骨分化。用油红O染色评估成脂分化。运用定量实时聚合酶链反应(Real-time PCR)检测成骨特异性基因(BMP-2、Runx2和Colla1)及成脂特异性基因(ap2、PPARγ)的表达。EGB对BMSCs的增殖无显著影响。然而,它增加了钙的积累,并显著促进了碱性磷酸酶的活性,尤其是当EGB浓度达到150 µg/mL时。EGB剂量依赖性地抑制BMSCs的成脂能力。随着EGB浓度的增加,成骨相关基因(BMP-2、Runx2、Colla1)过表达,而成脂相关基因如PPAR-γ和ap2的表达则降低。我们的数据证明,EGB抑制BMSCs的脂肪细胞分化并增强其成骨分化,但对BMSCs的增殖无影响。