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Enhancement of Bone Marrow-Derived Mesenchymal Stem Cell Osteogenesis and New Bone Formation in Rats by Obtusilactone A

机译:tus固内酯A增强大鼠骨髓间充质干细胞成骨和新骨形成

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摘要

The natural pure compound obtusilactone A (OA) was identified in Cinnamomum kotoense Kanehira & Sasaki, and shows effective anti-cancer activity. We studied the effect of OA on osteogenesis of bone marrow-derived mesenchymal stem cells (BMSCs). OA possesses biocompatibility, stimulates Alkaline Phosphatase (ALP) activity and facilitates mineralization of BMSCs. Expression of osteogenesis markers BMP2, Runx2, Collagen I, and Osteocalcin was enhanced in OA-treated BMSCs. An in vivo rat model with local administration of OA via needle implantation to bone marrow-residing BMSCs revealed that OA increased the new bone formation and trabecular bone volume in tibias. Micro-CT images and H&E staining showed more trabecular bone at the needle-implanted site in the OA group than the normal saline group. Thus, OA confers an osteoinductive effect on BMSCs via induction of osteogenic marker gene expression, such as BMP2 and Runx2 expression and subsequently elevates ALP activity and mineralization, followed by enhanced trabecular bone formation in rat tibias. Therefore, OA is a potential osteoinductive drug to stimulate new bone formation by BMSCs.
机译:天然纯化合物钝二甲内酯A(OA)在桂皮肉桂(Cinnamomum kotoense Kanehira&Sasaki)中鉴定出,并显示出有效的抗癌活性。我们研究了OA对骨髓源间充质干细胞(BMSCs)成骨的影响。 OA具有生物相容性,刺激碱性磷酸酶(ALP)活性并促进BMSC矿化。骨形成标记BMP2,Runx2,胶原I和骨钙蛋白的表达在OA处理的BMSC中得到增强。通过将OA通过针头植入局部骨髓的BMSC局部给药的体内大鼠模型显示,OA增加了胫骨中新的骨形成和小梁骨体积。 Micro-CT图像和H&E染色显示,与生理盐水组相比,OA组在针植入部位的小梁骨更多。因此,OA通过诱导成骨标记基因表达,例如BMP2和Runx2表达,对BMSC产生骨诱导作用,并随后增强ALP活性和矿化作用,然后增强大鼠胫骨中的小梁骨形成。因此,OA是一种潜在的骨诱导药物,可刺激BMSC刺激新的骨形成。

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