Paine Michael L, Luo Wen, Wang Hong-Jun, Bringas Pablo, Ngan Amanda Y W, Miklus Vetea G, Zhu Dan-Hong, MacDougall Mary, White Shane N, Snead Malcolm L
University of Southern California, School of Dentistry, Center for Craniofacial Molecular Biology, Los Angeles, California 90033, USA.
J Biol Chem. 2005 Sep 9;280(36):31991-8. doi: 10.1074/jbc.M502991200. Epub 2005 Jul 13.
The gene for dentin sialophosphoprotein produces a single protein that is post-translationally modified to generate two distinct extracellular proteins: dentin sialoprotein and dentin phosphoprotein. In teeth, dentin sialophosphoprotein is expressed primarily by odontoblast cells, but is also transiently expressed by presecretory ameloblasts. Because of this expression profile it appears that dentin sialophosphoprotein contributes to the early events of amelogenesis, and in particular to those events that result in the formation of the dentino-enamel junction and the adjacent "aprismatic" enamel. Using a transgenic animal approach we have extended dentin sialoprotein or dentin phosphoprotein expression throughout the developmental stages of amelogenesis. Overexpression of dentin sialoprotein results in an increased rate of enamel mineralization, however, the enamel morphology is not significantly altered. In wild-type animals, the inclusion of dentin sialoprotein in the forming aprismatic enamel may account for its increased hardness properties, when compared with bulk enamel. In contrast, the overexpression of dentin phosphoprotein creates "pitted" and "chalky" enamel of non-uniform thickness that is more prone to wear. Disruptions to the prismatic enamel structure are also a characteristic of the dentin phosphoprotein overexpressing animals. These data support the previous suggestion that dentin sialoprotein and dentin phosphoprotein have distinct functions related to tooth formation, and that the dentino-enamel junction should be viewed as a unique transition zone between enamel and the underlying dentin. These results support the notion that the dentin proteins expressed by presecretory ameloblasts contribute to the unique properties of the dentino-enamel junction.
牙本质涎磷蛋白基因产生一种单一蛋白质,该蛋白质在翻译后被修饰以生成两种不同的细胞外蛋白质:牙本质涎蛋白和牙本质磷蛋白。在牙齿中,牙本质涎磷蛋白主要由成牙本质细胞表达,但也由分泌前期成釉细胞短暂表达。由于这种表达模式,牙本质涎磷蛋白似乎在釉质形成的早期事件中起作用,特别是在那些导致牙釉质交界和相邻“无釉柱”釉质形成的事件中。使用转基因动物方法,我们在釉质形成的整个发育阶段扩展了牙本质涎蛋白或牙本质磷蛋白的表达。牙本质涎蛋白的过表达导致釉质矿化速率增加,然而,釉质形态没有明显改变。在野生型动物中,与整体釉质相比,在形成的无釉柱釉质中包含牙本质涎蛋白可能解释了其硬度增加的特性。相反,牙本质磷蛋白的过表达产生厚度不均匀的“凹陷”和“白垩状”釉质,更容易磨损。釉柱釉质结构的破坏也是牙本质磷蛋白过表达动物的一个特征。这些数据支持了先前的观点,即牙本质涎蛋白和牙本质磷蛋白在牙齿形成中具有不同的功能,并且牙釉质交界应被视为釉质和其下方牙本质之间的独特过渡区。这些结果支持了分泌前期成釉细胞表达的牙本质蛋白有助于牙釉质交界独特特性的观点。