Lu Li, Rao Li, Jia Huanhuan, Chen Jun, Lu Xingyan, Yang Guozhu, Li Qingnan, Lee Kenneth Ka Ho, Yang Li
School of Life Science and Biopharmacy, Guangdong Key Laboratory of Pharmaceutical Bioactive Substances, Guangdong Pharmaceutical University, Guangzhou, China.
Guangdong Key Laboratory of Laboratory Animals, Guangdong Laboratory Animals Monitoring Institute, Guangzhou, China.
J Cell Mol Med. 2017 Jul;21(7):1361-1372. doi: 10.1111/jcmm.13066. Epub 2017 Feb 3.
Activation of osteoblasts in bone formation and osteoclasts in bone resorption is important during the bone fracture healing process. There has been a long interest in identifying and developing a natural therapy for bone fracture healing. In this study, we investigated the regulation of osteoclast differentiation by baicalin, which is a natural molecule extracted from Eucommiaulmoides (small tree native to China). It was determined that baicalin enhanced osteoclast maturation and bone resorption activity in a dose-dependent manner. Moreover, this involves the activation of MAPK, increased Mitf nuclear translocation and up-regulation of downstream osteoclast-related target genes expression. The baicalin-induced effect on osteoclast differentiation can be mimicked by specific inhibitors of p-ERK (U0126) and the Mitf-specific siRNA, respectively. Protein-ligand docking prediction identified that baicalin might bind to RANK, which is the upstream receptor of p-ERK/Mitf signalling in osteoclasts. This indicated that RANK might be the binding target of baicalin. In sum, our findings revealed baicalin increased osteoclast maturation and function via p-ERK/Mitf signalling. In addition, the results suggest that baicalin can potentially be used as a natural product for the treatment of bone fracture.
在骨折愈合过程中,成骨细胞在骨形成中的激活以及破骨细胞在骨吸收中的激活非常重要。长期以来,人们一直对寻找和开发促进骨折愈合的天然疗法感兴趣。在本研究中,我们研究了黄芩苷(一种从中国本土小树杜仲中提取的天然分子)对破骨细胞分化的调节作用。结果表明,黄芩苷以剂量依赖性方式增强破骨细胞成熟和骨吸收活性。此外,这涉及丝裂原活化蛋白激酶(MAPK)的激活、小眼畸形相关转录因子(Mitf)核转位增加以及破骨细胞相关下游靶基因表达上调。黄芩苷诱导的破骨细胞分化效应可分别被p-细胞外信号调节激酶(p-ERK)的特异性抑制剂(U0126)和Mitf特异性小干扰RNA(siRNA)模拟。蛋白质-配体对接预测表明,黄芩苷可能与破骨细胞中p-ERK/Mitf信号的上游受体核因子κB受体活化因子(RANK)结合。这表明RANK可能是黄芩苷的结合靶点。总之,我们的研究结果表明黄芩苷通过p-ERK/Mitf信号通路增加破骨细胞成熟和功能。此外,结果表明黄芩苷有可能作为一种天然产物用于治疗骨折。