Effect of fluoride ion on proliferation of Vero cell line cells: growth acceleration by sodium fluoride.

A. Oguro, Nobuo Koizumi, K. Horii
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引用次数: 16

Abstract

The effect of fluoride ion (NaF) on proliferation was examined in Vero cells derived from kidney tissue of Cercopithecus aethiops. Fluoride ion concentrations in the growth medium of 0.1, 1, 10, and 100 ppm were employed in the first experiment and of 0.1, 0.2, 0.5, 1, 2, 5, 10, 20, 50, and 100 ppm in the second. Simplified replicate cultures were prepared and cultivated for about five days. After cultivation, cell growth was estimated by enumerating cell nuclei concentration. A relationship between cell proliferation and fluoride concentrations in the growth medium was confirmed statistically and details from control and experimental cell growth were investigated. Cell growth was accelerated by 17-18% with increasing fluoride ion concentrations of 1-10 ppm in first experiment. Maximum proliferation occurred at 2 ppm in the second experiment with a 22.6% rate of increase. Thereafter cell growth was reduced with increasing fluoride ion concentrations until near 100 ppm, at which concentration cell growth was completely stopped in both experiments. Introduction The relationship between cell proliferation and fluoride concentrations in growth medium has been studied by many investigators. In these studies here we have examined the proliferative potency and cellular metabolic alteration accompanying changes in fluoride concentrations. In 1960, Pace and Elrod, in their papers on effects of respiratory inhibitors, reported that 10-3M sodium fluoride (ca. 19 ppm F-) decreased L cell growth by 24%1). Berry and Trillwood reported in 1963 that 0.1-10.0 mg/l NaF (ca. 0.045-4.5 ppm F-) appreciably ca. 15-35%) depressed HeLa S-3 oxf and mouse fibroblast L (clone 12/oxf) cell growth2).However Albright and Armstrong et al. questioned these results. Then, Albright reported in 1964 that examining murine leukemic lymphoblasts, L5178Y strain, 3x 10-4M (5-6 ppm) Fdid not produce significant growth inhibition, and he also suggested that 4.4X 10-4 M (8-9 ppm) Fmight indicate incipient growth depressions). Armstrong et al. reported in 1965 that 10 ppm fluoride had no effect on HeLa and Minn. EE cell multiplication. But Berry and Trillwood responded that Armstrong et al. failed to get significant cell growth5). Against this criticism, Armstrong et al.immediately stated that 10 ppm Fdid not cause growth inhibition under satisfactory conditions6).Nias, who provided HeLa and L cells to Berry and Trillwood, concluded the arguments with his observation that 1 ppm NaF did not inhibit HeLa cell growth under experimental conditions similar to those of 55 * Department of Preventive Dentistry , Niigata University school of Dentistry(Director: Professor Kin-ichi HORII) *新 潟 大学歯学部予防歯科学教室(主 任:堀 井欣一教授) 昭和 56 年 8 月 12 日受付
氟离子对Vero细胞系细胞增殖的影响:氟化钠加速细胞生长。
本文研究了氟离子(NaF)对猪尾猿肾组织Vero细胞增殖的影响。在第一个实验中,生长培养基中的氟离子浓度分别为0.1、1、10和100 ppm,在第二个实验中,氟离子浓度分别为0.1、0.2、0.5、1、2、5、10、20、50和100 ppm。制备简化重复培养物,培养5天左右。培养后,通过计数细胞核浓度估计细胞的生长情况。从统计学上证实了细胞增殖与生长培养基中氟化物浓度之间的关系,并研究了对照和实验细胞生长的细节。在第一次实验中,当氟离子浓度为1 ~ 10 ppm时,细胞生长速度加快17 ~ 18%。在第二个实验中,最大增殖发生在2ppm,增长率为22.6%。此后,细胞生长随着氟离子浓度的增加而减少,直到接近100 ppm,在两个实验中,当氟离子浓度达到该浓度时,细胞生长完全停止。许多研究者研究了生长培养基中氟化物浓度与细胞增殖的关系。在这些研究中,我们检查了伴随氟化物浓度变化的增殖能力和细胞代谢变化。1960年,佩斯和埃尔罗德在他们关于呼吸抑制剂影响的论文中报告说,10-3M氟化钠(约19 ppm F-)使L细胞生长减少24%。Berry和Trillwood在1963年报道0.1-10.0 mg/l NaF(约0.045-4.5 ppm F-)明显约15-35%)抑制HeLa s - 3oxf和小鼠成纤维细胞l(克隆12/oxf)的生长2。然而,Albright和Armstrong等人质疑这些结果。随后,Albright在1964年报道,检测小鼠白血病淋巴母细胞L5178Y菌株,3x 10-4M (5-6 ppm) f没有产生显著的生长抑制,他还提出4.4X 10-4M (8-9 ppm) f可能表明早期生长抑制)。Armstrong等人在1965年报道,10ppm氟化物对HeLa和Minn没有影响。EE细胞增殖。但Berry和Trillwood回应说,Armstrong等人未能获得显著的细胞生长。针对这一批评,Armstrong等人立即声明,在令人满意的条件下,10ppm氟并没有引起生长抑制(6)。尼亚斯,他提供了海拉和L细胞浆果和Trillwood,得出的参数与他观察到1 ppm氟化钠不抑制海拉细胞生长在实验条件下类似于55 *预防口腔医学专业的部门,新泻大学牙科学院的教授(导演:Kin-ichi HORII) *新潟大学歯学部予防歯科学教室(主任:堀井欣一教授)昭和56年8月12日受付
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