Bawden J W, Rozell B, Wurtz T, Fouda N, Hammarström L
Center for Oral Biology, Karolinska Institute, Huddinge, Sweden.
J Dent Res. 1994 Aug;73(8):1429-36. doi: 10.1177/00220345940730080601.
Activation of the protein kinase C (PKC)-related signal transduction system has been associated with phenotypic expression in a wide variety of cell types. In in vitro studies, it has often been activated by relatively small increases in the Ca2+ concentration ([Ca2+]) in the medium. The studies reported here explored the hypothesis that localized increases in the extracellular [Ca2+] and activation of the PKC-related pathway may be involved in early dentin and enamel formation. Whole-head, freeze-dried sections through the developing molars of 5-day-old rats were evaluated by methods that localized non-crystalline Ca2+. Immunohistochemical methods were adapted for use with the freeze-dried sections, and two monoclonal antibodies were used to localize PKC alpha in the formative cells of the developing teeth. Low concentrations of extracellular Ca2+ were observed in the early, unmineralized dentin in the area of ameloblast differentiation. Increased concentrations occurred at the point of initial dentin mineralization, immediately before the beginning of enamel matrix deposition. PKC alpha was localized in the differentiating odontoblasts, at the beginning of dentin matrix deposition. It was intensely localized in the distal borders of the pre-ameloblasts, and appeared to redistribute in the cells during ameloblast differentiation. These observations suggest that local increases in the extracellular [Ca2+] and the PKC signal transduction pathway may be involved in key inductions in the early stages of dentin and enamel formation.
蛋白激酶C(PKC)相关信号转导系统的激活与多种细胞类型的表型表达有关。在体外研究中,它常常通过培养基中钙离子浓度([Ca2+])相对较小的升高而被激活。本文报道的研究探讨了这样一种假说,即细胞外[Ca2+]的局部升高和PKC相关途径的激活可能参与早期牙本质和釉质的形成。通过定位非结晶态Ca2+的方法对5日龄大鼠正在发育的磨牙进行全头冻干切片评估。免疫组织化学方法适用于冻干切片,使用两种单克隆抗体在正在发育牙齿的形成细胞中定位PKCα。在成釉细胞分化区域的早期未矿化牙本质中观察到低浓度的细胞外Ca2+。在牙本质开始矿化的点,即在釉质基质沉积开始之前,Ca2+浓度升高。PKCα在牙本质基质沉积开始时定位于分化中的成牙本质细胞。它强烈定位于前成釉细胞的远端边界,并且在成釉细胞分化过程中似乎在细胞内重新分布。这些观察结果表明,细胞外[Ca2+]的局部升高和PKC信号转导途径可能参与牙本质和釉质形成早期的关键诱导过程。