Selz T, Caverzasio J, Bonjour J P
Department of Medicine, University Hospital of Geneva, Switzerland.
Am J Physiol. 1991 Jun;260(6 Pt 1):E833-8. doi: 10.1152/ajpendo.1991.260.6.E833.
The influence of fluoride (F) on the transport of Pi was investigated in the osteoblast-like cell line UMR-106. Exposure of cells to F induced a dose-related stimulation of the Na-coupled Pi transport. Pi transport was significantly increased 6 h after 1 mM F incubation, with maximal response observed at 24 h (F 38.0 +/- 2.3, vehicle 19.8 +/- 1.2 pmol.micrograms DNA-1.4 min-1; P less than 0.001). Na-dependent alanine transport was not changed by F. The selective effect of F on Pi transport was not associated with changes in adenosine 3',5'-cyclic monophosphate, cell proliferation, or alkaline phosphatase activity. However, it was completely blunted by inhibiting translational processes with cycloheximide. Furthermore, F enhanced the stimulatory effect on Pi transport of various mitogens such as fetal calf serum, insulin, and insulin-like growth factor I. In conclusion, F can selectively enhance the activity of the Pi transport system present in the plasma membrane of UMR 106 osteoblast-like cells by a mechanism that probably involves newly synthetized proteins.
在成骨细胞样细胞系UMR - 106中研究了氟(F)对无机磷酸盐(Pi)转运的影响。将细胞暴露于F会诱导与剂量相关的钠耦联Pi转运刺激。在1 mM F孵育6小时后,Pi转运显著增加,在24小时观察到最大反应(F 38.0±2.3,载体对照组19.8±1.2 pmol·μg DNA⁻¹·4 min⁻¹;P<0.001)。F对钠依赖性丙氨酸转运没有影响。F对Pi转运的选择性作用与3',5'-环磷酸腺苷、细胞增殖或碱性磷酸酶活性的变化无关。然而,用放线菌酮抑制翻译过程可使其完全减弱。此外,F增强了各种有丝分裂原(如胎牛血清、胰岛素和胰岛素样生长因子I)对Pi转运的刺激作用。总之,F可能通过一种涉及新合成蛋白质的机制选择性增强UMR 106成骨细胞样细胞质膜中存在的Pi转运系统的活性。