Effect of leptin on differentiation of human dental stem cells

被引:34
作者
Um, S. [1 ]
Choi, J-R [1 ]
Lee, J-H [1 ]
Zhang, Q. [1 ]
Seo, B. M. [1 ]
机构
[1] Seoul Natl Univ, Dept Oral & Maxillofacial Surg, Sch Dent BK21, Biotooth Engn Lab,Dent Res Inst, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
dental stem cell; periodontal ligament stem cell; dental pulp stem cell; leptin; differentiation; HUMAN PERIODONTAL-LIGAMENT; MARROW STROMAL CELLS; HUMAN BONE-MARROW; ZUCKER RATS; OBESE GENE; RECEPTOR; MASS; MINERALIZATION; LOCALIZATION; OSTEOBLASTS;
D O I
10.1111/j.1601-0825.2011.01820.x
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
OBJECTIVES: Mesenchymal stem cells (MSCs) were identified in adult human periodontal ligament and dental pulp that are considered as potential stem cell sources for future clinical applications in dentistry. Leptin is known as an important regulator of mesenchymal differentiation. The objective of this study was to elucidate the role of leptin on proliferation and differentiation of dental MSCs. MATERIALS AND METHODS: Enhancement of cemento/odontoblastic differentiation of dental stem cells by leptin was confirmed by alizarin red S staining and alkaline phosphatase activity staining. In contrast, leptin reduced adipogenesis in both dental pulp stem cells (DPSCs) and periodontal ligament stem cells (PDLSCs) confirmed by oil red O staining and RT-PCR. The expression of adipogenic markers, lipoprotein lipase and proliferator-activated receptor gamma 2 (PPAR gamma 2), were suppressed in PDLSCs incubated on media supplemented with leptin for 2 weeks. RESULTS: Leptin had a relatively stronger osteogenesis promoting effect and adipogenesis suppressing effect in PDLSCs than in DPSCs. CONCLUSIONS: Collectively, leptin had a relatively stronger promoting effect on cemento/odontoblastic differentiation and a suppressing effect on adipogenesis in PDLSCs than in DPSCs. This study has provided evidence that leptin acts as an important modulator of dental MSCs differentiation. Oral Diseases (2011) 17, 662-669
引用
收藏
页码:662 / 669
页数:8
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