Chondrogenic differentiation of rat bone marrow mesenchymal stem cells induced by puerarin and tetrandrine

Xin-Ran Dong, Meng-Jiao Hu, Hui Pan, Ke-Feng Li, Yuan-Lu Cui
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引用次数: 1

Abstract

Abstract Objective: This study aims to clarify the effect of the active components puerarin and tetrandrine on the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs). Methods: Using network pharmacology, protein targets of puerarin and tetrandrine were predicted, and a database of cartilage formation targets was established. The protein target information related to disease was then collected, and the drug-targeting network was constructed by analyzing the protein–protein interactions. Genes related to chondrogenesis induced by puerarin and tetrandrine and chondroblast differentiation signaling pathways were searched. Finally, potential drug- and disease-related genes, as well as proteins, were screened and verified using real-time RT-PCR and western blotting. Results: Network pharmacological studies have shown that puerarin and tetrandrine are involved in BMSCs cartilage differentiation. The experimental results showed that puerarin and tetrandrine could regulate the expression of cartilage differentiation-related genes and proteins. Puerarin increased the protein expression of COL2A1, COL10A1, MMP13, and SOX-9, as well as the gene expression of Col2a1, Mmp13, Tgfb1, and Sox-9. Tetrandrine increased the protein expression of COL2A1, COL10A1, MMP13, and SOX-9, as well as the gene expression of Col10a1, Tgfb1, Sox-9, and Acan. The combination of puerarin and tetrandrine increased the protein expression of COL2A1, COL10A1, MMP13, and SOX-9 and the gene expression of Col2a1, Col10a1, Sox-9, and Acan. Conclusions: Puerarin, tetrandrine, and their combination can promote the proliferation of BMSCs and induce their differentiation into chondrocytes, and they are thus expected to be inducers of chondrogenic differentiation. These results suggest that puerarin and tetrandrine have potential therapeutic effects on osteoarthritis.
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葛根素和粉防己碱诱导大鼠骨髓间充质干细胞成软骨分化
摘要目的:研究葛根素和粉防己碱对骨髓间充质干细胞(BMSCs)成软骨分化的影响。方法:采用网络药理学方法预测葛根素和粉防己碱的蛋白靶点,建立软骨形成靶点数据库。然后收集与疾病相关的蛋白靶点信息,通过分析蛋白-蛋白相互作用构建药物靶向网络。寻找葛根素和粉防己碱诱导软骨形成的相关基因和成软骨分化信号通路。最后,利用实时RT-PCR和western blotting对潜在的药物和疾病相关基因以及蛋白质进行筛选和验证。结果:网络药理研究表明葛根素和粉防己碱参与骨髓间充质干细胞软骨分化。实验结果表明,葛根素和粉防己碱可调节软骨分化相关基因和蛋白的表达。葛根素增加了COL2A1、COL10A1、MMP13、SOX-9的蛋白表达以及COL2A1、MMP13、Tgfb1、SOX-9的基因表达。粉防甲素上调COL2A1、COL10A1、MMP13、SOX-9蛋白表达,上调COL10A1、Tgfb1、SOX-9、Acan基因表达。葛根素与粉防甲素联用可提高COL2A1、COL10A1、MMP13、SOX-9蛋白表达量以及COL2A1、COL10A1、SOX-9、Acan基因表达量。结论:葛根素、粉防己碱及其联合可促进骨髓间充质干细胞的增殖,诱导其向软骨细胞分化,有望成为软骨分化的诱导剂。这些结果提示葛根素和粉防己碱对骨关节炎有潜在的治疗作用。
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