Zhang Rui, Liang Qianyu, Kang Wenyan, Ge Shaohua
Department of Periodontology, School and Hospital of Stomatology, Shandong University & Shandong Provincial Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, No. 44-1 Wenhua Road West, Jinan, 250012, China.
Department of Endodontics, Hospital of stomatology, Zunyi medical University, No. 149 Dalian Road, Zunyi, 563000, China.
Cell Biol Int. 2020 Jan;44(1):70-79. doi: 10.1002/cbin.11202. Epub 2019 Jul 23.
Periodontitis is one of the main causes of tooth loss and has been confirmed as the sixth complication of diabetes. Metformin promotes the osteogenic differentiation of stem cells. Periodontal ligament stem cells (PDLSCs) are the best candidate stem cells for periodontal tissue regeneration. Herein, we aimed to identify the effects of metformin on the proliferation, migration, and osteogenic differentiation of PDLSCs in vitro. PDLSCs were isolated by limiting dilution, and their characteristics were assessed by colony formation assay and flow cytometry. Cell counting and migration assays were used to investigate the effects of metformin on proliferation and migration. The osteogenic differentiation ability of PDLSCs was detected by alkaline phosphatase (ALP) activity and Alizarin Red S staining. Gene and protein levels of osteogenesis-related markers were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and western blot analysis, respectively. Metformin treatment at 10 μM did not affect PDLSC proliferation, while at 50 and 100 μM, metformin time-dependently enhanced PDLSC proliferation and significantly increased cell numbers after 5 and 7 days of stimulation (P < 0.05). In addition, 50 μM metformin exhibited a maximal effect on migration, ALP activity, and mineral deposition (P < 0.05). Furthermore, 50 μM metformin significantly upregulated the gene expression levels of ALP, BSP, OPN, OCN, and Runx2 and the protein expression of ALP and Runx2 (P < 0.05). In summary, our study confirms that metformin facilitates the proliferation, migration, and osteogenic differentiation of PDLSCs in vitro and could be used as a new strategy for periodontal tissue regeneration.
牙周炎是牙齿缺失的主要原因之一,并且已被确认为糖尿病的第六大并发症。二甲双胍可促进干细胞的成骨分化。牙周膜干细胞(PDLSCs)是牙周组织再生的最佳候选干细胞。在此,我们旨在确定二甲双胍对体外培养的PDLSCs增殖、迁移和成骨分化的影响。通过有限稀释法分离PDLSCs,并通过集落形成试验和流式细胞术评估其特性。采用细胞计数和迁移试验来研究二甲双胍对增殖和迁移的影响。通过碱性磷酸酶(ALP)活性和茜素红S染色检测PDLSCs的成骨分化能力。分别通过定量实时聚合酶链反应(qRT-PCR)和蛋白质印迹分析测定成骨相关标志物的基因和蛋白水平。10μM的二甲双胍处理对PDLSCs增殖无影响,而在50和100μM时,二甲双胍呈时间依赖性地增强PDLSCs增殖,并在刺激5天和7天后显著增加细胞数量(P<0.05)。此外,50μM二甲双胍对迁移、ALP活性和矿化沉积具有最大效应(P<0.05)。此外,50μM二甲双胍显著上调ALP、BSP、OPN、OCN和Runx2的基因表达水平以及ALP和Runx2的蛋白表达(P<0.05)。总之,我们的研究证实二甲双胍在体外促进PDLSCs的增殖、迁移和成骨分化,可作为牙周组织再生的新策略。