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蛇床子素通过雌激素受体介导的BMP-2/ smad信号级联反应刺激骨髓间充质干细胞的成骨分化。

Cnidium lactone stimulates osteogenic differentiation of bone marrow mesenchymal stem cells via BMP-2/smad-signaling cascades mediated by estrogen receptor.

作者信息

Wang Zhao, Bao Hong-Wei

机构信息

Department of Orthopaedics, Jingjiang People's Hospital No. 28, Zhongzhou Road, Jingjiang, Taizhou 214500, Jiangsu Province, China.

出版信息

Am J Transl Res. 2019 Aug 15;11(8):4984-4991. eCollection 2019.

Abstract

Our aim was to study the osteogenic effect of cnidium lactone for bone marrow mesenchymal stem cells (BMSCs) and its potential mechanism. BMSCs were isolated and identified by flow cytometry and multidirectional differentiation capacity. Cell Counting Kit-8 (CCK-8) was used to identify the optimal concentration of cnidium lactone. Alkaline Phosphatase (ALP) and Alizarin Red S (ARS) was performed to identify whether cnidium lactone has effect on osteogenesis at early and late phase respectively. Moreover, we used estrogen receptor antagonist, ICI182780, to identify the receptor of cnidium lactone. The expression of Runt-related transcription factor 2 (RUNX2), Osterix (OSX), osteopontin (OPN), estrogen receptor (ER), Smad4, p-Smad1, Smad1 and bone morphogenetic protein 2 (BMP-2) protein were measured by PCR and western blot. Cnidium lactone (2 μM) demonstrated increased osteogenesis after osteogenic inducible medium (OIM) induction, as evidenced by more ALP activity and mineralization. When blocked with ICI182780, osteogenesis capacity was decreased. Moreover, the polymerase chain reaction (PCR) and western blotting results indicated that cnidium lactone enhanced ER, BMP2, Smad1, Smad4, RUNX2, OSX, and OPN expression and Smad1 phosphorylation. Cnidium lactone can effectively stimulates osteogenic differentiation of BMSCs via BMP-2/Smad-Signaling cascades mediated by ER.

摘要

我们的目的是研究蛇床子素对骨髓间充质干细胞(BMSCs)的成骨作用及其潜在机制。通过流式细胞术和多向分化能力分离并鉴定BMSCs。使用细胞计数试剂盒-8(CCK-8)确定蛇床子素的最佳浓度。分别进行碱性磷酸酶(ALP)和茜素红S(ARS)检测,以鉴定蛇床子素在早期和晚期对成骨是否有作用。此外,我们使用雌激素受体拮抗剂ICI182780来确定蛇床子素的受体。通过PCR和蛋白质印迹法检测Runt相关转录因子2(RUNX2)、osterix(OSX)、骨桥蛋白(OPN)、雌激素受体(ER)、Smad4、磷酸化Smad1、Smad1和骨形态发生蛋白2(BMP-2)蛋白的表达。在成骨诱导培养基(OIM)诱导后,蛇床子素(2μM)显示出成骨增加,表现为更多的ALP活性和矿化。当用ICI182780阻断时,成骨能力下降。此外,聚合酶链反应(PCR)和蛋白质印迹结果表明,蛇床子素增强了ER、BMP2、Smad1、Smad4、RUNX2、OSX和OPN的表达以及Smad1的磷酸化。蛇床子素可通过由ER介导的BMP-2/Smad信号级联有效地刺激BMSCs的成骨分化。

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