Department of Orofacial Sciences, University of California, San Francisco, PO Box 0422, 521 Parnassus Avenue, Room S704, San Francisco, CA 94143-0422, USA.
J Dent Res. 2011 Jun;90(6):782-7. doi: 10.1177/0022034511398273. Epub 2011 Mar 1.
Enamel biomineralization results in a release of protons into the enamel matrix, causing an acidification of the local microenvironment. This acidification, which may be enhanced by more rapid mineral deposition in the presence of fluoride, must be neutralized by the overlying ameloblasts. The electrogenic sodium bicarbonate co-transporter NBCe1 has been localized in mouse ameloblasts, and has been proposed to have a role in matrix pH regulation. In this study, transcript analysis by PCR showed NBCe1-A present in human ameloblasts, whereas mouse ameloblasts expressed NBCe1-B. In situ hybridization and qPCR in mouse and fetal human incisors showed that NBCe1 mRNA was up-regulated as ameloblasts differentiated. Ingestion of 50 ppm fluoride resulted in an up-regulation of NBCe1 mRNA in maturation-stage mouse ameloblasts in vivo, as compared with controls. NBCe1 expression was up-regulated by low pH, but not by fluoride, in human ameloblast-lineage cells in vitro. The up-regulation of NBCe1 in vivo as enamel maturation and mineralization progressed provides evidence that NBCe1 participates in pH modulation during enamel formation. Up-regulation of NBCe1 in fluorosed maturation ameloblasts in vivo, with no effect of fluoride in vitro, supports the hypothesis that fluoride-enhanced mineral deposition results in acidification of the mineralizing enamel matrix.
釉质生物矿化导致质子释放到釉质基质中,导致局部微环境酸化。这种酸化,在氟存在的情况下可能由于更快速的矿物质沉积而增强,必须由覆盖的成釉细胞中和。电生钠碳酸氢盐共转运体 NBCe1 已在小鼠成釉细胞中定位,并被提议在基质 pH 调节中发挥作用。在这项研究中,通过 PCR 的转录分析显示 NBCe1-A 存在于人成釉细胞中,而小鼠成釉细胞表达 NBCe1-B。在小鼠和胎生人切牙中的原位杂交和 qPCR 显示,随着成釉细胞分化,NBCe1 mRNA 上调。与对照组相比,体内摄入 50 ppm 氟化物导致成熟阶段的小鼠成釉细胞中 NBCe1 mRNA 的上调。NBCe1 表达在体外被低 pH 上调,但不受氟化物的影响。在体内釉质成熟和矿化过程中 NBCe1 的上调提供了证据,表明 NBCe1 参与了釉质形成过程中的 pH 调节。体内氟斑牙成熟成釉细胞中 NBCe1 的上调,体外氟化物无作用,支持氟化物增强矿物质沉积导致矿化釉质基质酸化的假说。