School of Pharmaceutical Sciences and Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, No. 1168 Chunrongxi Road, Chenggong District, Kunming, 650500, Yunnan, People's Republic of China.
J Nat Med. 2019 Jan;73(1):262-272. doi: 10.1007/s11418-018-1242-6. Epub 2018 Sep 7.
Abnormal osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) has been correlated with the pathogenesis of osteoporosis. Geraniin, a polyphenolic compound isolated from Phyllanthus amarus, is effective in preventing osteoporosis, but the mechanisms of action of geraniin and the impact of osteoporotic condition on drug action are not known. In this study we compared the proliferation and osteoblastic differentiation potential of BMSCs from normal rats with that from osteoporotic rats, and examined the responses of both BMSCs to geraniin in parallel. BMSCs of rats subjected to ovariectomy or sham operation were isolated and treated with geraniin. Cell proliferation was measured by CCK-8 assay. Osteoblastic differentiation was quantified by Alizarin Red S staining and alkaline phosphatase assay. Nuclear translocation of β-catenin was monitored by immunofluorescent staining. Expression of β-catenin was determined by Western blot and quantitative real-time polymerase chain reaction. Results showed that the proliferation and osteoblast formation of osteoporotic BMSCs decreased in comparison to that of normal BMSCs. Geraniin enhanced proliferation and osteoblastic differentiation of both BMSCs, but the responses of osteoporotic BMSCs to geraniin were less than those of normal BMSCs. Expression and nuclear accumulation of β-catenin in osteoporotic BMSCs were found to be diminished. Geraniin increased nuclear translocation and expression of β-catenin in both BMSCs. This study associated the osteogenic effect of geraniin to activation of Wnt/β-catenin signaling, and provided rationale for pharmacological investigation of geraniin in osteoporosis prevention and treatment.
骨髓间充质干细胞(BMSCs)的异常成骨分化与骨质疏松症的发病机制有关。栀子素是从叶下珠中分离得到的一种多酚化合物,在预防骨质疏松症方面有效果,但栀子素的作用机制以及骨质疏松症对药物作用的影响尚不清楚。在这项研究中,我们比较了正常大鼠和骨质疏松大鼠的 BMSCs 的增殖和成骨分化潜能,并平行研究了两者对栀子素的反应。通过卵巢切除术或假手术处理大鼠,分离 BMSCs 并进行栀子素处理。通过 CCK-8 法测量细胞增殖。通过茜素红 S 染色和碱性磷酸酶测定来量化成骨分化。通过免疫荧光染色监测 β-连环蛋白的核易位。通过 Western blot 和实时定量聚合酶链反应确定 β-连环蛋白的表达。结果表明,与正常 BMSCs 相比,骨质疏松大鼠的 BMSCs 的增殖和成骨形成减少。栀子素增强了两种 BMSCs 的增殖和成骨分化,但骨质疏松大鼠 BMSCs 对栀子素的反应不及正常 BMSCs。在骨质疏松大鼠 BMSCs 中发现β-连环蛋白的表达和核积累减少。栀子素增加了两种 BMSCs 中 β-连环蛋白的核易位和表达。本研究将栀子素的成骨作用与 Wnt/β-连环蛋白信号通路的激活联系起来,为栀子素在骨质疏松症预防和治疗中的药理研究提供了依据。