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积雪草苷通过 Wnt 通路诱导人牙周膜细胞的成骨分化。

Asiaticoside induces osteogenic differentiation of human periodontal ligament cells through the Wnt pathway.

机构信息

Mineralized Tissue Research Unit, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.

Department of Anatomy, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Periodontol. 2018 May;89(5):596-605. doi: 10.1002/JPER.17-0471.

Abstract

BACKGROUND

Asiaticoside is a compound isolated from Herb Centella asiatica, which has been shown to promote osteogenic differentiation of human periodontal ligament (hPDL) cells. This study investigated the molecular mechanism underlying the asiaticoside-induced osteogenic differentiation of hPDL cells.

METHODS

hPDL cells were incubated with various concentrations of asiaticoside to test cell viability by MTT assay. The mRNA expression levels were analyzed by using quantitative real-time polymerase chain reaction (PCR). Osteogenic differentiation was determined by alkaline phosphatase activity assay and alizarin red staining. The subcellular localization of β-catenin was analyzed by both immunofluorescence and western blot.

RESULTS

The results showed that asiaticoside had no effect on the cell viability at any of the tested concentrations. Real-time PCR revealed that osterix (OSX) and dentin matrix protein1 (DMP1) mRNA were significantly enhanced by asiaticoside treatment. Alkaline phosphatase activity and in vitro mineralization were also significantly induced. Interestingly, asiaticoside dose-dependently increased WNT3A mRNA expression, but not WNT5A and WNT10B. The activation of Wnt signaling was shown to result in nuclear accumulation of β-catenin as evaluated by immunofluorescence staining and western blot analysis. Pre-treatment with recombinant human Dickkopf1 (rhDKK1) inhibited asiaticoside-induced β-catenin nuclear translocation and osteoblast marker gene expression. Moreover, rhDKK1 attenuated asiaticoside-induced DMP1 protein expression.

CONCLUSION

The data demonstrate that asiaticoside induces osteogenic differentiation of hPDL cells by activating the Wnt/β-catenin signaling pathway. The findings suggest that asiaticoside could be used as a novel therapeutic drug for periodontal tissue regeneration.

摘要

背景

积雪草苷是从积雪草中分离得到的一种化合物,已被证明能促进人牙周膜(hPDL)细胞的成骨分化。本研究探讨了积雪草苷诱导 hPDL 细胞成骨分化的分子机制。

方法

用不同浓度的积雪草苷孵育 hPDL 细胞,通过 MTT 法检测细胞活力。采用实时定量聚合酶链反应(PCR)分析 mRNA 表达水平。通过碱性磷酸酶活性测定和茜素红染色检测成骨分化。通过免疫荧光和 Western blot 分析β-连环蛋白的亚细胞定位。

结果

结果表明,积雪草苷在任何测试浓度下对细胞活力均无影响。实时 PCR 显示,osterix(OSX)和牙本质基质蛋白 1(DMP1)mRNA 被积雪草苷处理显著增强。碱性磷酸酶活性和体外矿化也显著诱导。有趣的是,积雪草苷剂量依赖性地增加 WNT3A mRNA 表达,但不增加 WNT5A 和 WNT10B。免疫荧光染色和 Western blot 分析显示,Wnt 信号的激活导致β-连环蛋白的核积累。用重组人 Dickkopf1(rhDKK1)预处理抑制了积雪草苷诱导的β-连环蛋白核转位和成骨标记基因表达。此外,rhDKK1 减弱了积雪草苷诱导的 DMP1 蛋白表达。

结论

数据表明,积雪草苷通过激活 Wnt/β-连环蛋白信号通路诱导 hPDL 细胞的成骨分化。研究结果表明,积雪草苷可作为牙周组织再生的新型治疗药物。

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