Nie Bin, Zhou Shaoqiong, Fang Xin, Li Wei, Wang Bin, Guan Siming
Department of Geriatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
J Huazhong Univ Sci Technolog Med Sci. 2012 Dec;32(6):818-822. doi: 10.1007/s11596-012-1040-4. Epub 2012 Dec 28.
Recent studies showed that activation of Wnt/β-catenin pathway promoted the differentiation of osteoblast-like cells in the arterial calcification, but its mechanism remains unknown. In this study, the hypothesis that Wnt/β-catenin pathway promotes the differentiation of osteoblast-like cells by upregulating the expression of receptor activator of NF-κB ligand (RANKL) was examined. LiCl was used to activate the Wnt/β-catenin pathway. The differentiation of osteoblast-like cells was observed by Von Kossa staining, calcium content assay, alkaline phosphatase (ALP) activity assay, and detection of osteocalcin expression. Real-time PCR was performed to detect the expression of RANKL and osteoprotegerin (OPG, the decoy receptor of RANKL) during the osteoblast-like cell differentiation. Different concentrations of OPG were added to the culture media respectively to inhibit the function of RANKL, and the change in the differentiation of osteoblast-like cells was evaluated. The results showed that when the Wnt/β-catenin pathway was activated by LiCl, the expression of RANKL was significantly increased, which coincided with the differentiation of osteoblast-like cells (P<0.05), and the OPG treatment could partly attenuate the promoting effect of Wnt/β-catenin pathway on the differentiation of osteoblast-like cells (P<0.05), but it failed to completely abolish such effect. It was concluded that activation of Wnt/β-catenin pathway promotes the differentiation of osteoblast-like cells by both RANKL-dependent and RANKL-independent mechanisms.
近期研究表明,Wnt/β-连环蛋白信号通路的激活促进了动脉钙化中类成骨细胞的分化,但其机制尚不清楚。在本研究中,对Wnt/β-连环蛋白信号通路通过上调核因子κB受体活化因子配体(RANKL)的表达促进类成骨细胞分化这一假说进行了验证。使用氯化锂激活Wnt/β-连环蛋白信号通路。通过冯科萨染色、钙含量测定、碱性磷酸酶(ALP)活性测定以及骨钙素表达检测来观察类成骨细胞的分化情况。在类成骨细胞分化过程中,采用实时定量聚合酶链反应检测RANKL和骨保护素(OPG,RANKL的诱饵受体)的表达。分别向培养基中添加不同浓度的OPG以抑制RANKL的功能,并评估类成骨细胞分化的变化。结果显示,当用氯化锂激活Wnt/β-连环蛋白信号通路时,RANKL的表达显著增加,这与类成骨细胞的分化相一致(P<0.05),并且OPG处理可部分减弱Wnt/β-连环蛋白信号通路对类成骨细胞分化的促进作用(P<0.05),但未能完全消除这种作用。得出的结论是,Wnt/β-连环蛋白信号通路的激活通过RANKL依赖和RANKL非依赖机制促进类成骨细胞的分化。