Enamel matrix derivative enhances the proliferation and osteogenic differentiation of human periodontal ligament stem cells on the titanium implant surface

被引:31
作者
Li, Guang [1 ,2 ]
Hu, Jing [3 ]
Chen, Hui [4 ]
Chen, Liang [4 ]
Zhang, Na [2 ]
Zhao, Lisheng [1 ]
Wen, Ning [1 ]
Yang, Yongjin [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Stomatol, Beijing 100853, Peoples R China
[2] PLA, Dept Stomatol, Rocket Force Gen Hosp, Beijing 100088, Peoples R China
[3] Beijing PLA, Dept Stomatol, Mil Gen Hosp, Beijing, Peoples R China
[4] Jinan Stomatol Hosp, Dept Endodont, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Akt; Enamel matrix derivative; mTOR; osteogenic differentiation; osteoblasts; periodontal ligament stem cells; OSTEOBLAST-LIKE CELLS; IN-VITRO; BONE-MARROW; GENE-EXPRESSION; REGENERATION; PROMOTES; PATHWAY; RAPAMYCIN; CAPACITY; BEHAVIOR;
D O I
10.1080/15476278.2017.1331196
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Periodontal ligament stem cells (PDLSCs) have mesenchymal-stem-cells-like qualities, and are considered as one of the candidates of future clinical application in periodontal regeneration therapy. Enamel matrix derivative (EMD) is widely used in promoting periodontal regeneration. However, the effects of EMD on the proliferation and osteogenic differentiation of human PDLSCs grown on the Ti implant surface are still no clear. Therefore, this study examined the effects of EMD on human PDLSCs in vitro. Human PDLSCs were isolated from healthy participants, and seeded on the surface of Ti implant disks and stimulated with various concentrations of EMD. Cell proliferation was determined with Cell Counting Kit-8 (CCK-8). The osteogenic differentiation of PDLSCs was evaluated by the measurement of alkaline phosphatase (ALP) activity, Alizarin red staining, and real-time polymerase chain reaction (qRT-PCR) and Western blotting, respectively. The results indicated that EMD at concentrations (5-60 mu g/ml) increased the viability and proliferation of PDLSCs. The treatment with 30 and 60 mu g/ml of EMD significantly elevated ALP activity, augmented mineralized nodule formation and calcium deposition, and upregulated the mRNA and protein levels of Runx-2 and osteocalcin (OCN) in the PDLSCs grown on the Ti surface. Further investigation found that EMD treatment did not change the protein levels of phosphatidylinositol-3-kinase (PI3K), p-PI3K, Akt and mTOR, but significantly upregulated the phosphorylated levels of Akt and mTOR. Collectively, these results suggest that EMD stimulation can promote the proliferation and osteogenic differentiation of PDLSCs grown on Ti surface, which is possibly associated with the activation of Akt/mTOR signaling pathway.
引用
收藏
页码:103 / 113
页数:11
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