7th Ward, Department of Rheumatology and Immunology, Xi'an No.5 Hospital, Xi'an, 710082, Shaanxi, P.R. China.
5th Ward, Department of Rheumatology and Immunology, Xi'an No.5 Hospital, Xi'an, 710082, Shaanxi, P.R. China.
J Orthop Surg Res. 2024 Oct 22;19(1):678. doi: 10.1186/s13018-024-05174-0.
Our study focused on the effects and molecular mechanisms of kaempferol, a major active component of Eucommia ulmoides Oliver (EUO), on the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs).
Target molecules for EUO, osteoarthritis, and osteogenic differentiation were identified through network pharmacology analysis. BMSCs were isolated and treated with various concentrations of kaempferol. Optimal concentration was determined through MTT assays. Osteogenic differentiation was assessed using alkaline phosphatase (ALP) and Alizarin Red S staining, while osteogenic markers (Collagen I, RUNX2, and OPN) and CAV-1 expression were analyzed using RT-qPCR and Western blot. The effects of combined treatment with kaempferol and an overexpression vector for CAV-1 (oe-CAV-1) on osteogenic differentiation were also observed.
Network pharmacology analysis identified kaempferol as the primary active component influencing CAV-1 targeted in subsequent experiments. It was found that 10 µM kaempferol was optimal for treating BMSCs. Post-treatment, significant increases in ALP activity and calcium deposition were observed, along with elevated expression of osteogenic markers, and decreased CAV-1. Overexpression of CAV-1 significantly reversed the promotive effects of kaempferol on BMSC osteogenic differentiation, effectively inhibiting the process.
Collectively, kaempferol promotes osteogenic differentiation in BMSCs by inhibiting CAV-1 expression.
本研究聚焦于山柰酚(Eucommia ulmoides Oliver 的主要活性成分之一)对骨髓间充质干细胞(BMSCs)成骨分化的作用及其分子机制。
通过网络药理学分析鉴定 EUO、骨关节炎和成骨分化的靶分子。分离和用不同浓度的山柰酚处理 BMSCs。通过 MTT 测定确定最佳浓度。通过碱性磷酸酶(ALP)和茜素红 S 染色评估成骨分化,同时通过 RT-qPCR 和 Western blot 分析成骨标志物(Collagen I、RUNX2 和 OPN)和 CAV-1 表达。还观察了山柰酚与 CAV-1 过表达载体(oe-CAV-1)联合处理对成骨分化的影响。
网络药理学分析确定山柰酚是后续实验中影响 CAV-1 靶向的主要活性成分。结果发现,10 µM 的山柰酚是治疗 BMSCs 的最佳浓度。处理后,ALP 活性和钙沉积显著增加,同时成骨标志物表达升高,CAV-1 减少。CAV-1 的过表达显著逆转了山柰酚对 BMSC 成骨分化的促进作用,有效抑制了该过程。
总之,山柰酚通过抑制 CAV-1 的表达促进 BMSCs 的成骨分化。