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高糖促进人牙周膜成纤维细胞的成骨分化能力。

High glucose promotes the osteogenic differentiation capability of human periodontal ligament fibroblasts.

作者信息

Seubbuk Sujiwan, Sritanaudomchai Hathaitip, Kasetsuwan Julalux, Surarit Rudee

机构信息

Molecular Medicine Program, Faculty of Science, Mahidol University, Ratchthewi, Bangkok 10400, Thailand.

Department of Oral Biology, Faculty of Dentistry, Mahidol University, Ratchthewi, Bangkok 10400, Thailand.

出版信息

Mol Med Rep. 2017 May;15(5):2788-2794. doi: 10.3892/mmr.2017.6333. Epub 2017 Mar 16.

DOI:10.3892/mmr.2017.6333
PMID:28447734
Abstract

Periodontal ligament fibroblasts (PDLFs) are important cells, which are involved in maintaining tooth integrity. Diabetes has been found to be associated with periodontal disease in a bidirectional manner. The aim of the present study was to investigate the stemness properties of human PDLFs (HPDLFs) in high glucose conditions. HPDLFs were analyzed for their osteogenic differentiation capacity by inducing the cells with osteogenic medium in various glucose concentrations. The gene expression was then examined using reverse transcription‑quantitative polymerase chain reaction analysis, and examinations of alkaline phosphatase activity and nodule formation were performed. The results of the gene expression analysis revealed that high glucose media induced the expression of NANOG, octamer-binding transcription factor 4, (sex determining region Y)‑box 2, cluster of differentiation 166 (CD166), PERIOSTIN and β‑CATENIN following culture of the cells for 3 days. Alkaline phosphatase activity increased following 14 days in the high glucose condition. In addition, higher numbers of calcified nodules were formed on day 28 in the group cultured with high glucose. The results showed that high glucose induced bone formation by elevating the expression of stem cell markers, particularly CD166, and this induction may be regulated through β-CATENIN.

摘要

牙周膜成纤维细胞(PDLFs)是重要的细胞,参与维持牙齿的完整性。糖尿病已被发现与牙周疾病存在双向关联。本研究的目的是调查高糖条件下人牙周膜成纤维细胞(HPDLFs)的干性特性。通过在不同葡萄糖浓度的成骨培养基中诱导细胞,分析HPDLFs的成骨分化能力。然后使用逆转录-定量聚合酶链反应分析检测基因表达,并进行碱性磷酸酶活性和结节形成检测。基因表达分析结果显示,细胞培养3天后,高糖培养基诱导了NANOG、八聚体结合转录因子4、(性别决定区Y)-盒2、分化簇166(CD166)、骨膜蛋白和β-连环蛋白的表达。在高糖条件下培养14天后,碱性磷酸酶活性增加。此外,在高糖培养组中,第28天形成的钙化结节数量更多。结果表明,高糖通过提高干细胞标志物尤其是CD166的表达诱导骨形成,并且这种诱导可能通过β-连环蛋白进行调节。

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