Lee Hye-Kyung, Park Ji-Won, Seo You-Mi, Kim Ha Hoon, Lee Gene, Bae Hyun-Sook, Park Joo-Cheol
Department of Oral Histology-Developmental Biology and Dental Research Institute, School of Dentistry, Seoul National University, 101 Daehagro, Chongro-gu, Seoul, 110-749, Republic of Korea.
Department of Orthodontics, School of Dentistry, Seoul National University, 101 Daehagro, Chongro-gu, Seoul, 110-749, Republic of Korea.
J Mol Histol. 2016 Jun;47(3):345-51. doi: 10.1007/s10735-016-9676-1. Epub 2016 Apr 20.
For the dentin regeneration, dental epithelial cells are indispensible and must possess odontoblastic induction capability. Epithelial cell-like stem cells were recently identified in human deciduous dental pulp (DPESCs). However, their cellular characteristics remain poorly defined. The purpose of this study was to characterize DPESCs compared to HAT-7 ameloblastic cells. Expression levels of ameloblast-specific markers [odontogenic ameloblast-associated protein (Odam), matrix metalloproteinase (Mmp)-20, amelogenin, and ameloblastin] were detected in DPESCs. Co-culturing odontoblastic MDPC-23 cells with DPESCs increased expression of odontoblast differentiation markers (Dmp1 and Dspp) from days 4 to 10, while the expression of bone sialoprotein rapidly decreased. MDPC-23 cells cultured in DPESC-conditioned medium (CM) showed increased Dspp promoter activity compared with control MDPC-23 cultures. Mineralization was first observed in the CM groups from day 4 and proceeded rapidly until day 14, whereas mineralized nodules were found from day 7 in control media-cultured cells. In conclusion, DPESCs in human deciduous pulp possess ameloblast-like characteristics and differentiation properties, and substances derived from DPESCs promote odontoblastic differentiation. Thus, our results indicate that DPESCs can be a realistic epithelial source for use in odontoblastic induction and dentin formation of dental mesenchymal cells.
对于牙本质再生而言,牙上皮细胞不可或缺且必须具备成牙本质细胞诱导能力。最近在人乳牙牙髓中鉴定出了上皮样干细胞(DPESCs)。然而,它们的细胞特征仍不清楚。本研究的目的是将DPESCs与HAT-7成釉细胞进行比较,以表征DPESCs。在DPESCs中检测了成釉细胞特异性标志物[成牙本质细胞相关蛋白(Odam)、基质金属蛋白酶(Mmp)-20、釉原蛋白和成釉蛋白]的表达水平。从第4天到第10天,将成牙本质细胞MDPC-23与DPESCs共培养可增加成牙本质细胞分化标志物(Dmp1和Dspp)的表达,而骨涎蛋白的表达迅速下降。与对照MDPC-23培养物相比,在DPESC条件培养基(CM)中培养的MDPC-23细胞显示Dspp启动子活性增加。从第4天开始在CM组中首次观察到矿化,并迅速进行直至第14天,而在对照培养基培养的细胞中从第7天开始发现矿化结节。总之,人乳牙牙髓中的DPESCs具有成釉细胞样特征和分化特性,并且源自DPESCs的物质促进成牙本质细胞分化。因此,我们的结果表明,DPESCs可以作为一种切实可行的上皮来源,用于牙间充质细胞的成牙本质细胞诱导和牙本质形成。
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