Kim Hye-Sun, Lee Dong-Seol, Lee Ji Hyun, Kang Min-Suh, Lee Na-Rae, Kim Heung-Joong, Ko Jea-Seung, Cho Moon-Il, Park Joo-Cheol
Department of Oral Anatomy and 2nd Stage of BK21, College of Dentistry, Chosun University, 375 Seo-sug Dong, Dong-Gu, 501-759 Gwang-Ju, Republic of Korea.
Arch Oral Biol. 2009 Jan;54(1):71-9. doi: 10.1016/j.archoralbio.2008.09.011. Epub 2008 Nov 11.
Cementum is an important mineralized tissue in root formation, however, the precise mechanism of cementum formation remains undetermined. The purpose of this study was to evaluate the effect of odontoblast conditioned media (CM) and dentin non-collagenous proteins (dNCPs) on the differentiation and mineralization of cementoblastic OCCM-30 cells.
The CM of ameloblastic ALCs, odontoblastic MDPC-23 and OD-11, osteoblastic MG-63, and fibroblastic NIH3T3 cells were transferred to OCCM-30 cells. dNCPs were extracted directly from porcine and human dentin and applied to OCCM-30 cells. The results were evaluated through the analysis of the morphologic appearance, expression of cementum matrix genes, and the formation of mineralized nodules in vitro.
dNCPs hardly influenced proliferation, cell cycle modification, and chemotaxis of cementoblasts. Mineralization of cementoblasts was accelerated with dNCPs and CM from odontoblastic MDPC-23 and OD-11. RT-PCR analysis revealed the earlier and stronger expression of bone sialoprotein (BSP), alkaline phosphatase (ALP), and osteocalcin (OC) mRNAs in the MDPC23- and OD11-CM-treated OCCM-30 cells than those in the control OCCM-30 cells. The level of gene expression was also significantly higher in the dNCP-treated group than the control group.
These results suggest that dentin matrix proteins, or the secreted products of odontoblasts, induced cementoblast differentiation and mineralization. These findings may contribute to the development of a periodontal treatment that includes cementum regeneration.
牙骨质是牙根形成过程中一种重要的矿化组织,然而,牙骨质形成的确切机制仍未明确。本研究的目的是评估成牙本质细胞条件培养基(CM)和牙本质非胶原蛋白(dNCPs)对牙骨质细胞系OCCM - 30细胞分化和矿化的影响。
将成釉细胞系ALCs、成牙本质细胞系MDPC - 23和OD - 11、成骨细胞系MG - 63以及成纤维细胞系NIH3T3细胞的CM转移至OCCM - 30细胞。直接从猪和人牙本质中提取dNCPs并应用于OCCM - 30细胞。通过分析体外形态学表现、牙骨质基质基因表达及矿化结节形成来评估结果。
dNCPs对牙骨质细胞的增殖、细胞周期改变和趋化性影响不大。来自成牙本质细胞系MDPC - 23和OD - 11的dNCPs和CM加速了牙骨质细胞的矿化。逆转录 - 聚合酶链反应(RT - PCR)分析显示,与对照OCCM - 30细胞相比,经MDPC23 - CM和OD11 - CM处理的OCCM - 30细胞中骨涎蛋白(BSP)、碱性磷酸酶(ALP)和骨钙素(OC)mRNA表达更早且更强。dNCP处理组的基因表达水平也显著高于对照组。
这些结果表明牙本质基质蛋白或成牙本质细胞的分泌产物可诱导牙骨质细胞分化和矿化。这些发现可能有助于开发包括牙骨质再生的牙周治疗方法。