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首页> 外文期刊>Biological trace element research >Effects of Sodium Fluoride Treatment In Vitro on Cell Proliferation, BMP-2 and BMP-3 Expression in Human Osteosarcoma MG-63 Cells
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Effects of Sodium Fluoride Treatment In Vitro on Cell Proliferation, BMP-2 and BMP-3 Expression in Human Osteosarcoma MG-63 Cells

机译:体外氟化钠处理对人骨瘤Mg-63细胞中细胞增殖,BMP-2和BMP-3表达的影响

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Chronic excessive fluoride intake may cause fluorosis, which chiefly manifests as bone damage (or skeletal fluorosis). However, the molecular mechanism of skeletal fluorosis has not been clarified up to the present. The objective of this study was to analyze the effects of fluoride treatment on two of bone morphogenetic protein family member (BMP-2 and BMP-3) expression and cell viability using human osteosarcoma MG-63 cells as a model. Sodium fluoride (NaF) had pro-proliferation effects at relatively moderate concentration, with 5 x 10(3) mu mol/L having the best effects. At 2 x 10(4) mu mol/L, NaF inhibits cell proliferation. BMP-2 and BMP-3 expression was significantly induced by 5 x 10(3) mu mol/L NaF and, to lesser extent, by 2 x 10(4) mu mol/L NaF. Correspondingly, mothers against decapentaplegic homolog 1 (Smad-1) increased at both doses of NaF, which indicated the BMP signaling pathway was activated. Notable increases in secreted alkaline phosphatase (ALP) were observed when cells were treated with 5 x 10(3) mu mol/L NaF. A BMP specific inhibitor LDN193189 suppressed cell proliferation induced by 5 x 10(3) mu mol/L NaF. Also, 2 x 10(4) mu mol/L NaF induced apoptosis but likely through a mechanism unrelated to the BMP pathway. Collectively, data show that NaF had dose-dependent effects on cell proliferation as well as BMP-2 and BMP-3 expression in MG-63 cells and suggested that cell proliferation enhanced by NaF-induced BMP members may be a molecular mechanism underlying skeletal fluorosis.
机译:慢性过量氟化物摄入可能导致氟中毒,主要表现为骨损伤(或骨骼氟中毒)。然而,骨骼氟中毒的分子机制尚未澄清到现在。本研究的目的是分析氟化物处理对两种骨形态发生蛋白家族成员(BMP-2和BMP-3)表达和使用人骨肉瘤MG-63细胞作为模型的含量活力。氟化钠(NAF)具有相对中等浓度的促进效果,具有5×10(3)μmol/ L具有最佳效果。在2×10(4)mu mol / l,Naf抑制细胞增殖。 BMP-2和BMP-3表达显着诱导5×10(3)摩尔/升NAF,较小程度,均多2×10(4)μmol/ L Naf。相应地,对抗脱尾屈曲同源物的母亲(Smad-1)增加了两种剂量的NAF,这表明了BMP信号通路被激活。当用5×10(3)mu mol / L Naf处理细胞时,观察到分泌的碱性磷酸酶(ALP)的显着增加。 BMP特异性抑制剂LDN193189抑制了5×10(3)μmol/ L Naf诱导的细胞增殖。此外,2×10(4)mu mol / l Naf诱导细胞凋亡,但可能通过与BMP途径无关的机制。统称,数据表明,NAF对Mg-63细胞中的BMP-2和BMP-3表达具有剂量依赖性影响,并提出了通过NAF诱导的BMP成员增强的细胞增殖可以是骨骼氟中缺失的分子机制。

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