Veron M H, Couble M L, Magloire H
Laboratoire de Développement et de Pathologie des Tissus Dentaires, CNRS-UPR 412, Faculté d'Odontologie, Lyon, France.
Calcif Tissue Int. 1993 Jul;53(1):38-44. doi: 10.1007/BF01352013.
Human dental pulp cells were cultured in fluoridated mediums (0, 1, 10, 25 ppm) in order to study the biological effect of the ion regarding the cellular metabolism: cell growth, alkaline phosphatase (ALP) activity, and protein synthesis. The results indicated a decrease of the cell growth at 25 ppm and a dose-dependent decrease of the ALP activity. Type I collagen immunoperoxidase staining, radioimmunoassay quantitation, and analysis of type I and III collagens mRNA levels showed an inhibition of collagen production and gene expression. In contrast, fibronectin production and gene expression were not affected by fluoride. The treatment did not influence the qualitative pattern of the different mRNA species. Of the three collagen chains, the alpha 1(I) was the most affected. These data suggest that fluoride does not exert a general depletive effect on human dental pulp cells but rather a selective inhibition on collagen production.
为研究氟离子对细胞代谢(细胞生长、碱性磷酸酶(ALP)活性和蛋白质合成)的生物学效应,将人牙髓细胞培养于含氟培养基(0、1、10、25 ppm)中。结果表明,25 ppm时细胞生长下降,且ALP活性呈剂量依赖性降低。I型胶原免疫过氧化物酶染色、放射免疫分析定量以及I型和III型胶原mRNA水平分析显示,胶原产生和基因表达受到抑制。相比之下,纤连蛋白的产生和基因表达不受氟的影响。该处理不影响不同mRNA种类的定性模式。在三条胶原链中,α1(I)受影响最大。这些数据表明,氟对人牙髓细胞并非产生普遍的消耗性作用,而是对胶原产生具有选择性抑制作用。