Gao Jing, Huang Wenming
Hua Xi Kou Qiang Yi Xue Za Zhi. 2016 Apr;34(2):200-4. doi: 10.7518/hxkq.2016.02.019.
To observe the dynamic changes of membrane-bound proton-translocating ATPase (F-ATPase) in the development of dental caries, the expression of Streptococcus mutans F-ATPase under different pH concentrations and during the development of dental caries is analyzed.
Streptococcus mutans cultured under different pH (pH4.0-7.0) concentrations and containing 5% glucose and no glucose containing BHI were collected. RNA was extracted. Subsequently, F-ATPase gene was detected using real-time polymerase chain reaction. Male Wistar rats were divided randomly into caries group and control group. The rats in the caries group were fed caries feed and 5% glucose water, whereas those of control group were fed normal feed. Total RNA was extracted from plaque samples, which were collected from rats' oral cavity every two weeks. F-ATPase gene was detected by real-time PCR. In the 11th week, the upper and lower jaw bone specimens of rats were taken, and molar caries damage assessed.
The expression of F-ATPase in the caries group was higher than that in the control group (P<0.05). In addition, the gene was expressed highest in pH5.0 and the lowest in pH4.0 (P<0.05). 2) The expression of F-ATPase progressively increased during the caries development in both groups; expression in the caries group was higher than that in control group (P<0.05).
Acid-resisting viru-lence factor F-ATPase is related closely with the incidence and development of dental caries.
观察膜结合质子转运ATP酶(F-ATP酶)在龋齿发生发展过程中的动态变化,分析变形链球菌F-ATP酶在不同pH浓度及龋齿发生发展过程中的表达情况。
收集在含5%葡萄糖及不含葡萄糖的BHI培养基中于不同pH(pH4.0 - 7.0)浓度下培养的变形链球菌。提取RNA。随后,采用实时聚合酶链链链链反应检测F-ATP酶基因。将雄性Wistar大鼠随机分为龋齿组和对照组。龋齿组大鼠喂饲致龋饲料及5%葡萄糖水,而对照组大鼠喂饲正常饲料。每两周从大鼠口腔采集菌斑样本,提取总RNA。通过实时PCR检测F-ATP酶基因。在第11周,取大鼠上下颌骨标本,评估磨牙龋齿损害情况。
龋齿组F-ATP酶的表达高于对照组(P<0.05)。此外,该基因在pH5.0时表达最高,在pH4.0时表达最低(P<0.05)。2)两组在龋齿发展过程中F-ATP酶的表达均逐渐增加;龋齿组的表达高于对照组(P<0.05)。
耐酸性毒力因子F-ATP酶与龋齿的发生发展密切相关。