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beta-Ecdysterone Induces Osteogenic Differentiation in Mouse Mesenchymal Stem Cells and Relieves Osteoporosis

机译:β-蜕皮甾酮诱导小鼠骨髓间充质干细胞成骨分化并缓解骨质疏松症

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The effect on bone tissue of beta-ecdysterone, a type of ecdysteroid found in many plants, has not been previously investigated. In this study, we found that beta-ecdysterone treatment significantly induced alkaline phosphatase (ALP) activity in mesenchymal stem cells in a dose-dependent manner. Real-time polymerase chain reaction (PCR) showed that Runx2, osteocalcin, and type I collagen expression also increased. ICI182780, a specific estrogen receptor antagonist, inhibited the upregulation of ALP activity. Moreover, beta-ecdysterone promoted estrogen receptor (ER) reporter gene activity; however, ICI182780 reversed its effect, suggesting that beta-ecdysterone has stimulatory effects on osteogenic differentiation via the Ell. Furthermore, beta-ecdysterone alleviated osteoporosis symptoms in a mouse model without obvious side effects. Therefore beta-ecdysterone may be a promising candidate drug for the treatment of osteoporosis.
机译:以前尚未研究过β-蜕皮甾酮(一种在许多植物中发现的蜕皮甾类化合物)对骨骼组织的作用。在这项研究中,我们发现β-蜕皮甾酮治疗以剂量依赖的方式显着诱导间充质干细胞中的碱性磷酸酶(ALP)活性。实时聚合酶链反应(PCR)显示Runx2,骨钙素和I型胶原表达也增加。 ICI182780,一种特定的雌激素受体拮抗剂,抑制ALP活性的上调。此外,β-蜕皮甾酮可促进雌激素受体(ER)报告基因活性。然而,ICI182780逆转了其作用,表明β-蜕皮甾酮对通过Ell诱导的成骨分化具有刺激作用。此外,β-蜕皮甾酮可减轻小鼠模型的骨质疏松症症状,而无明显副作用。因此,β-蜕皮甾酮可能是治疗骨质疏松的有前途的候选药物。

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