Metformin facilitates the proliferation, migration, and osteogenic differentiation of periodontal ligament stem cells in vitro

被引:40
|
作者
Zhang, Rui [1 ,2 ,3 ,4 ]
Liang, Qianyu [1 ,2 ,3 ]
Kang, Wenyan [1 ,2 ,3 ]
Ge, Shaohua [1 ,2 ,3 ]
机构
[1] Shandong Univ, Sch & Hosp Stomatol, Dept Periodontol, 44-1 Wenhua Rd West, Jinan 250012, Peoples R China
[2] Shandong Prov Key Lab Oral Tissue Regenerat, 44-1 Wenhua Rd West, Jinan 250012, Peoples R China
[3] Shandong Engn Lab Dent Mat & Oral Tissue Regenera, 44-1 Wenhua Rd West, Jinan 250012, Peoples R China
[4] Zunyi Med Univ, Hosp Stomatol, Dept Endodont, 149 Dalian Rd, Zunyi 563000, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
metformin; migration; osteogenic differentiation; periodontal ligament stem cells; proliferation; ACTIVATED PROTEIN-KINASE; ENDOGENOUS STEM; DISEASE; MECHANISMS;
D O I
10.1002/cbin.11202
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 mu M did not affect PDLSC proliferation, while at 50 and 100 mu M, metformin time-dependently enhanced PDLSC proliferation and significantly increased cell numbers after 5 and 7 days of stimulation (P < 0.05). In addition, 50 mu M metformin exhibited a maximal effect on migration, ALP activity, and mineral deposition (P < 0.05). Furthermore, 50 mu M 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.
引用
收藏
页码:70 / 79
页数:10
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