Sun Liting, Yu Fuqing, Xu Zhihua, Zeng Xinmei, Ferreri Miro, Han Bo
College of Veterinary Medicine, China Agricultural University, Beijing 100094, PR of China.
Acta Biol Hung. 2010 Mar;61(1):52-63. doi: 10.1556/ABiol.61.2010.1.6.
Objective of this study was to assess the quantification of osteocalcin (OCN) expression by ovine osteoblasts cultured with different concentrations of sodium fluoride (F) and sodium selenite (Se) to evaluate the interaction of these agents on OCN expression in vitro . We wanted to demonstrate a possible protective effect of selenium on the toxic effect of fluoride. Osteoblasts were isolated by complete trypsin and collagenase digestion from ovine calvarial bone and cultured in DMEM supplemented with 15% FBS at 37 degrees C in a humidified 5% CO 2 incubator. Identified osteoblasts were divided into one control group (C) and eight experimental groups, which were exposed to different concentrations of sodium fluoride (F; 0, 0.5, 1 mM) sodium selenite (Se; 0, 0.1, 1 microM). At different time points after treatment total RNA was extracted and reverse transcribed into first-strand cDNA. OCN mRNA was indirectly measured by real-time fluorescent quantitative PCR (qPCR). OCN mRNA expression in F 1 mM with Se 1 microM group was found to have a high peak at day seven and was lower before and afterwards. Expression of OCN mRNA in all groups except control could be promoted by F and/or Se showing a general upregulation. Furthermore, the toxicity from excessive exposure of osteoblast with F could be circumvented by usage of moderate concentration of Se. Osteoblasts cultured in vitro may have stressful responses to F and Se at the first few days. Low concentrations of Se inhibit the toxic effects of high concentrations of F. Therefore, F and Se could be used as antagonistic factors, which could regulate osteocalcin expression.
本研究的目的是评估用不同浓度的氟化钠(F)和亚硒酸钠(Se)培养的绵羊成骨细胞骨钙素(OCN)表达的定量情况,以评估这些试剂在体外对OCN表达的相互作用。我们想证明硒对氟中毒作用可能具有保护作用。通过用完全胰蛋白酶和胶原酶消化从绵羊颅骨分离成骨细胞,并在补充有15%胎牛血清的DMEM中于37℃、5%二氧化碳饱和湿度的培养箱中培养。鉴定后的成骨细胞分为一个对照组(C)和八个实验组,分别暴露于不同浓度的氟化钠(F;0、0.5、1 mM)和亚硒酸钠(Se;0、0.1、1 microM)。处理后的不同时间点提取总RNA并逆转录为第一链cDNA。通过实时荧光定量PCR(qPCR)间接测量OCN mRNA。发现1 mM F与1 microM Se组的OCN mRNA表达在第7天有一个高峰,在此之前和之后较低。除对照组外,所有组中F和/或Se均可促进OCN mRNA表达,呈现普遍上调。此外,使用中等浓度的Se可规避成骨细胞过度暴露于F的毒性。体外培养的成骨细胞在最初几天可能对F和Se有应激反应。低浓度的Se可抑制高浓度F的毒性作用。因此,F和Se可作为拮抗因子,调节骨钙素表达。