Department of Orthopedics, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150000, P.R. China.
Department of Orthopedics, The First Hospital of Qiqihar, Qiqihar, Heilongjiang 161000, P.R. China.
Int J Mol Med. 2014 Feb;33(2):351-8. doi: 10.3892/ijmm.2013.1576. Epub 2013 Dec 5.
It has been reported that sodium fluoride (NaF) suppresses the proliferation and induces apoptosis of chondrocytes. However, the cellular and molecular mechanisms of the effect have not been elucidated. Therefore, the aim of this study was to evaluate the mechanisms of the effects of NaF on primary cultured rat chondrocytes in vitro. Chondrocytes were treated with NaF at concentrations of 0, 1.5, 2.0, 2.5, 3.0, 3.5 and 4.0 mM. Cell viability decreased and the rate of apoptotic cells increased significantly with the gradient concentration of NaF in a time- and dose-dependent manner. Electron microscopy revealed cytoplasmic, organelle and nuclear alterations in the ultrastructure of chondrocytes exposed to various NaF concentrations. The cell cycle distribution was analyzed by flow cytometry, and the results indicated that NaF induced G2 cell cycle arrest. Western blotting was used to detect the apoptotic pathways. Downregulation of the Bcl-2 protein and upregulation of Bax, cleaved caspase-9, -12 and -3 proteins suggested that NaF was capable of inducing apoptosis through the mitochondrial and endoplasmic reticulum pathways. The results also showed that the levels of hypoxia-inducible factor 1α (HIF-1α), sex determining region Y box gene 9 (Sox9) and the collagen II (Col II) protein of the NaF groups were lower compared to those of the control groups. Thus, NaF may induce apoptosis through the downregulation of HIF-1α and disrupt the synthesis of extracellular matrix (ECM) through the downregulation of HIF-1α via the Sox9 pathway in primary cultured rat chondrocytes.
据报道,氟化钠(NaF)可抑制软骨细胞的增殖并诱导其凋亡。然而,其作用的细胞和分子机制尚未阐明。因此,本研究旨在评估 NaF 对体外原代培养大鼠软骨细胞的影响机制。软骨细胞用浓度为 0、1.5、2.0、2.5、3.0、3.5 和 4.0mM 的 NaF 处理。细胞活力随 NaF 浓度梯度呈时间和剂量依赖性降低,凋亡细胞率显著增加。电镜显示,暴露于不同 NaF 浓度的软骨细胞的细胞质、细胞器和核结构发生超微结构改变。通过流式细胞术分析细胞周期分布,结果表明 NaF 诱导 G2 细胞周期阻滞。Western blot 用于检测凋亡途径。Bcl-2 蛋白下调和 Bax、切割的 caspase-9、-12 和 -3 蛋白上调表明 NaF 能够通过线粒体和内质网途径诱导细胞凋亡。结果还表明,与对照组相比,NaF 组的低氧诱导因子 1α(HIF-1α)、性别决定区 Y 框基因 9(Sox9)和胶原蛋白 II(Col II)蛋白水平较低。因此,NaF 可能通过下调 HIF-1α 诱导细胞凋亡,并通过 Sox9 途径下调 HIF-1α 破坏细胞外基质(ECM)的合成。