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核因子κB受体激活剂配体在Wnt/β-连环蛋白通路促进成骨样细胞分化中的作用

Implication of receptor activator of NF-κB ligand in Wnt/β-catenin pathway promoting osteoblast-like cell differentiation.

作者信息

Nie Bin, Zhou Shaoqiong, Fang Xin, Li Wei, Wang Bin, Guan Siming

机构信息

Department of Geriatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2012 Dec;32(6):818-822. doi: 10.1007/s11596-012-1040-4. Epub 2012 Dec 28.

Abstract

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.

摘要

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。

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