Shanghai Journal of Stomatology ›› 2014, Vol. 23 ›› Issue (5): 519-523.

• Basic Study • Previous Articles     Next Articles

Effect of fluoride on the viability and apoptosis of ameloblasts in vitro

MA Lin1, ZHANG Ying1, ZHONG Ming2, ZHU Li2, ZHANG Kai-qiang1, GU He-feng1, LIU Lu1, ZHANG Si-yu1, CHENG Rui-bo1   

  1. 1.Department of Preventive Dentistry; 2.Department of Central Laboratory, School of Stomatology, China Medical University. Shenyang 110002, Liaoning Province, China
  • Received:2013-10-21 Revised:2013-12-10 Online:2014-10-20 Published:2015-02-04
  • Supported by:
    ; Supported by National Natural Science Foundation of China (81072245) and Natural Science Foundation of Liaoning Province (20102278)

Abstract: PURPOSE: To evaluate the effect of fluoride on viability of rat ameloblasts in vitro. METHODS: The ameloblasts of rat was exposed to different concentrations of NaF (0, 0.4, 0.8, 1.6, 3.2, 6.4 mmol/L) for 24, 48 and 72 hours. CCK-8 assays were performed to measure the cells proliferation; The morphology of apoptosis was observed by Hoechst 33258 staining and the rate of apoptosis was determined by flow cytometry. The data was analyzed using SPSS 13.0 software package. RESULTS: ①The proliferation of ameloblasts was increased when concentrations of NaF between 0.4 mmol/L and 0.8 mmol/L, whereas inhibited at 1.6 mmol/L NaF and above. The effects were in time-dependent manner.②Cells in the 1.6 mmol/L NaF groups showed unclear karyorrhexis and apoptotic cell morphology. The effects were in concentration-dependent manner. CONCLUSIONS: ① Fluoride has two-phase effects to ameloblasts: At low doses, it promoted cell proliferation while at high doses it had negative effects. ②1.6 mmol/L NaF could induce apoptosis of ameloblasts.

Key words: Fluoride, Ameloblast, CCK8, Flow cytometry, Hoechst 33258 fluorescence staining