College of Veterinary Medicine, China Agricultural University, 100193 Beijing, China.
Biochem Biophys Res Commun. 2011 Jul 15;410(4):910-5. doi: 10.1016/j.bbrc.2011.06.094. Epub 2011 Jun 17.
Chronic excessive fluoride intake is known to be toxic and can lead to fluorosis and bone pathologies. However, the cellular mechanisms underlying NaF-induced cytotoxicity in osteoblasts are not well understood. The objectives of this study were to determine the effects of fluoride treatment on MC3T3-E1 osteoblastic cell viability, cell cycle analysis, apoptosis and the expression levels of bcl-2 family members: bcl-2 and bax. MC3T3-E1 cells were treated with 10(-5); 5 × 10(-5); 10(-4); 5 × 10(-4) and 10(-3)M NaF for up to 48 h. NaF was found to reduce cell viability in a temporal and concentration dependent manner and promote apoptosis even at low concentrations (10(-5)M). This increased apoptosis was due to alterations in the expression of both pro-apoptotic bax and anti-apoptotic bcl-2. The net result was a decrease in the bcl-2/bax ratio which was found at both the mRNA and protein levels. Furthermore, we also noted that NaF-induced S-phase arrest during the cell cycle of MC3T3-E1 cells. These data suggest that fluoride-induced osteoblast apoptosis is mediated by direct effects of fluoride on the expression of bcl-2 family members.
慢性过量氟化物摄入是有毒的,并可能导致氟中毒和骨骼病理学。然而,氟化物诱导成骨细胞细胞毒性的细胞机制尚不清楚。本研究的目的是确定氟化物处理对 MC3T3-E1 成骨细胞活力、细胞周期分析、细胞凋亡和 bcl-2 家族成员(bcl-2 和 bax)表达水平的影响。将 MC3T3-E1 细胞用 10(-5); 5 × 10(-5); 10(-4); 5 × 10(-4) 和 10(-3)M NaF 处理长达 48 小时。发现 NaF 以时间和浓度依赖的方式降低细胞活力,并在低浓度(10(-5)M)时促进细胞凋亡。这种增加的细胞凋亡是由于促凋亡 bax 和抗凋亡 bcl-2 的表达改变所致。在 mRNA 和蛋白质水平上都发现 bcl-2/bax 比值降低。此外,我们还注意到,NaF 诱导的 MC3T3-E1 细胞周期中的 S 期阻滞。这些数据表明,氟化物诱导的成骨细胞凋亡是由氟化物对 bcl-2 家族成员表达的直接作用介导的。