Takano Y, Ozawa H, Crenshaw M A
Cell Tissue Res. 1986;243(1):91-9. doi: 10.1007/BF00221856.
Enzymatic activities of calcium-magnesium dependent adenosine triphosphatase (Ca-ATPase) and nonspecific alkaline phosphatase (ALPase) were localized at the initial calcification sites of dentin and enamel of rat incisor teeth using electron-microscopic cytochemistry. Ca-ATPase was localized in the Golgi cisternae, cytoplasmic vesicles and along the outer surface of the presecretory and secretory ameloblasts, whereas it was totally absent from the odontoblasts in the pulp. Inversely, ALPase reaction was localized along the outer surface of the odontoblasts, but almost completely absent from the ameloblasts. Diffuse extracellular reactions of both enzymes were distributed throughout the unmineralized fibrous matrix of mantle dentin in which a large number of matrix vesicles were scattered. Both Ca-ATPase and ALPase reactions, which appeared in the matrix vesicles in the process of formation of mantle dentin, became most conspicuous at the site of initial dentin calcification. At this stage, an intense Ca-ATPase reaction also appeared along some of the collagen fibrils adjacent to the reactive matrix vesicles. No ALPase reaction was localized along these Ca-ATPase reactive collagen fibrils. Our observations suggest strongly that Ca-ATPase in the matrix vesicles originates from the inner enamel epithelium and/or preameloblasts whereas ALPase originates from the odontoblasts in the pulp. The importance of the coexistence of both enzymes for the control of initial calcification of dental hard tissues is suggested.
利用电子显微镜细胞化学技术,在大鼠切牙牙本质和釉质的初始钙化部位定位了钙镁依赖性三磷酸腺苷酶(Ca - ATPase)和非特异性碱性磷酸酶(ALPase)的酶活性。Ca - ATPase定位于高尔基体潴泡、细胞质小泡以及分泌前和成釉细胞的外表面,而牙髓中的成牙本质细胞中则完全没有。相反,ALPase反应定位于成牙本质细胞的外表面,而成釉细胞中几乎完全没有。两种酶的弥漫性细胞外反应分布在罩牙本质未矿化的纤维基质中,其中散布着大量基质小泡。在罩牙本质形成过程中出现在基质小泡中的Ca - ATPase和ALPase反应,在初始牙本质钙化部位最为明显。在此阶段,一些与反应性基质小泡相邻的胶原纤维上也出现了强烈的Ca - ATPase反应。这些Ca - ATPase反应性胶原纤维上没有ALPase反应定位。我们的观察结果强烈表明,基质小泡中的Ca - ATPase起源于内釉上皮和/或成釉细胞前体细胞,而ALPase起源于牙髓中的成牙本质细胞。这表明两种酶共存对于控制牙齿硬组织初始钙化的重要性。