Kaipatur N R, Murshed M, McKee M D
Faculty of Dentistry, McGill University, 3640 University Street, Montreal, QC, Canada H3A 2B2.
J Dent Res. 2008 Sep;87(9):839-44. doi: 10.1177/154405910808700907.
Extracellular matrix (ECM) mineralization is regulated by mineral ion availability, proteins, and other molecular determinants. To investigate protein regulation of mineralization in tooth dentin and cementum, and in alveolar bone, we expressed matrix Gla protein (MGP) ectopically in bones and teeth in mice, using an osteoblast/odontoblast-specific 2.3-kb Col1a1 promoter. Mandibles were analyzed by radiography, micro-computed tomography, light microscopy, histomorphometry, and transmission electron microscopy. While bone and tooth ECMs were established in the Col1a1-Mgp mice, extensive hypomineralization was observed, with values of unmineralized ECM from four- to eight-fold higher in dentin and alveolar bone when compared with that in wild-type tissues. Mineralization was virtually absent in tooth root dentin and cellular cementum, while crown dentin showed "breakthrough" areas of mineralization. Acellular cementum was lacking in Col1a1-Mgp teeth, and unmineralized osteodentin formed within the pulp. These results strengthen the view that bone and tooth mineralization is critically regulated by mineralization inhibitors.
细胞外基质(ECM)矿化受矿质离子可用性、蛋白质及其他分子决定因素的调控。为研究牙本质、牙骨质及牙槽骨矿化的蛋白质调控机制,我们利用成骨细胞/成牙本质细胞特异性的2.3 kb Col1a1启动子,在小鼠的骨骼和牙齿中异位表达基质Gla蛋白(MGP)。通过X线摄影、显微计算机断层扫描、光学显微镜、组织形态计量学及透射电子显微镜对下颌骨进行分析。虽然Col1a1-Mgp小鼠的骨骼和牙齿ECM已形成,但观察到广泛的矿化不足,与野生型组织相比,牙本质和牙槽骨中未矿化ECM的值高出4至8倍。牙根牙本质和细胞性牙骨质几乎没有矿化,而冠部牙本质出现了矿化“突破”区域。Col1a1-Mgp牙齿缺乏无细胞牙骨质,牙髓内形成了未矿化的骨样牙本质。这些结果强化了骨和牙齿矿化受矿化抑制剂严格调控这一观点。