Department of Endemic Diseases Control and Prevention, Hangzhou Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
Biol Trace Elem Res. 2013 Oct;155(1):142-9. doi: 10.1007/s12011-013-9770-0. Epub 2013 Aug 7.
The BMP/Smad signaling pathway plays an important role in the viability and differentiation of osteoblast; however, it is not clear whether this pathway is involved in the fluoride-induced osteoblast differentiation. In this study, we investigated the role of BMP/Smad signaling pathway in fluoride-induced osteoblast-like Saos-2 cells differentiation. Cells were exposed to fluoride of different concentrations (0, 0.1, 0.2, 0.4, 0.8, and 1.6 mM), and cell proliferation was determined using WST assays. The expression of osteoblast marker genes such as osteocalcin (BGP) and bone alkaline phosphatase (BALP) were detected by qRT-PCR. We found that fluoride enhanced the proliferation of Saos-2 cells in a dose-dependent manner and 0.2 mM of fluoride resulted in a higher expression of osteoblast marker genes. In addition, immunofluorescence analysis showed that the promotion effects of 0.2 mM of fluoride on Saos-2 cells differentiation were associated with the activation of the BMP/Smad pathway. Expression of phosphorylated Smad1/5(p-Smad1/5) was higher in cells exposed to 0.2 mM of fluoride. Plasmid expression vectors encoding the short hairpin RNA (shRNA) targeting Smad4 gene were used to block the BMP/Smad pathway, which resulted in a significantly reduced expression of BGP and BALP as well as their corresponding mRNA. The mRNA levels after transfection remained low even in the presence of fluoride. The present results reveal that BMP/Smad signaling pathway was altered during the period of osteogenesis, and that the activities of p-Smad1/5 were required for Saos-2 cells viability and differentiation induced by fluoride.
BMP/Smad 信号通路在成骨细胞的存活和分化中发挥着重要作用;然而,目前尚不清楚该通路是否参与了氟化物诱导的成骨细胞分化。在这项研究中,我们研究了 BMP/Smad 信号通路在氟化物诱导的成骨样 Saos-2 细胞分化中的作用。将细胞暴露于不同浓度(0、0.1、0.2、0.4、0.8 和 1.6 mM)的氟化物中,通过 WST 测定法确定细胞增殖。通过 qRT-PCR 检测骨钙素(BGP)和骨碱性磷酸酶(BALP)等成骨细胞标记基因的表达。我们发现氟化物以剂量依赖性方式增强 Saos-2 细胞的增殖,而 0.2 mM 的氟化物导致成骨细胞标记基因的表达更高。此外,免疫荧光分析表明,0.2 mM 氟化物对 Saos-2 细胞分化的促进作用与 BMP/Smad 通路的激活有关。暴露于 0.2 mM 氟化物的细胞中磷酸化 Smad1/5(p-Smad1/5)的表达更高。使用编码靶向 Smad4 基因的短发夹 RNA(shRNA)的质粒表达载体阻断 BMP/Smad 通路,导致 BGP 和 BALP 及其相应 mRNA 的表达显著降低。即使存在氟化物,转染后的 mRNA 水平仍保持较低。这些结果表明,BMP/Smad 信号通路在成骨过程中发生改变,p-Smad1/5 的活性对于氟化物诱导的 Saos-2 细胞活力和分化是必需的。