Chemokine-Like Receptor 1 信号通路对双氢睾酮诱导小鼠骨密度增加的影响
Effects of Chemokine-Like Receptor 1 Signal Pathway on Mice Induced by Dihydrotestosterone Increased Bone Mineral Density
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摘要: 文章通过在小鼠体内注射双氢睾酮和 2α-萘酰乙基三甲基碘化铵以及体外水平培养诱导骨髓间充质干细胞, 研究 G 蛋白偶联受体趋化因子样受体 1(Chemokine-Like Receptor 1, CMKLR1)基因缺失对双氢睾酮诱导的骨髓间充质干细胞向成骨分化的影响。结果发现 CMKLR1 基因缺失后骨髓间充质干细胞的成骨分化率降低, 双氢睾酮刺激后, 野生型小鼠的骨髓间充质干细胞成骨分化有所提升, 而CMKLR1 缺失小鼠的骨髓间质干细胞成骨分化变化不大, 说明 CMKLR1 基因的缺失影响了双氢睾酮对骨细胞的作用。Abstract: To study the effect of dihydrotestosterone on the osteogenic differentiation of bone marrow mesenchymal stem cells after chemokine-like receptor 1 (CMKLR1) gene knockout, dihydrotestosterone and N, N, N-trimethyl-γ-oxo-2-naphthalenepropanaminium, monoiodide were injected in mice and induced bone marrow mesenchymal stem cells in vitro. The results showed that osteogenic differentiation rate decreased after CMKLR1 gene knockout and increased when dihydrotestosterone was injected in wild type mice bone marrow mesenchymal stem cells. However, there was no significant change in CMKLR1 knockout mice. The result indicated that the effect of dihydrotestosterone on bone cells was affected by the deletion of CMKLR1.