College of Medicine, University of Saskatchewan, Health Sciences Building, Saskatoon, Canada.
Biochem Cell Biol. 2011 Aug;89(4):377-86. doi: 10.1139/o11-034. Epub 2011 Jul 26.
The effect of fluoride treatment on the expression of a panel of osteogenic and stress markers in Stage 55 premetamorphic Xenopus larvae was examined at the precise onset of replacement of the larval cartilaginous skeleton with bone. A dosing regimen of 10 mmol/L sodium fluoride over 8 days was followed, during which time larvae developed to Stage 58, when the process of progressive ossification takes place in the vertebral column and membranous bones of the skull, pelvic, and pectoral girdles and portions of the appendicular skeleton. Markers of bone formation, including COL1A1, the transcription factors Osterix, RUNX2-II, and matrix metalloproteinases MMP1 and MMP13, decreased relative to age-matched controls, though the osteoblast marker BGLAP was not significantly altered. Expression of the pro-osteoclastogenic factor RANKL decreased, whereas expression of the anti-osteoclastogenic factor osteoprotegerin increased. Altered expression of oxidative stress markers, with the exception of superoxide dismutase, was generally not observed. These data demonstrate the potent effects of fluoride on the expression of factors required for osteoblast and osteoclast differentiation, as well as on the expression of osteoblast products, including MMP1 and collagen. Importantly, these effects were observed in the absence of significant changes in the expression of oxidative stress markers. The results provide the first molecular insights into the mechanisms underlying skeletal fluorosis in a whole organism developmental model.
研究了氟化物处理对处于 55 期前变态期的非洲爪蟾幼虫中成骨和应激标志物表达的影响,此时正是幼虫的软骨骨骼被骨骼替代的起始阶段。在 8 天的时间里,用 10mmol/L 的氟化钠进行处理,在此期间,幼虫发育到 58 期,此时脊柱和颅骨、骨盆和胸带以及部分附肢骨骼中的骨骼进行渐进性骨化。成骨标志物,包括 COL1A1、转录因子 Osterix、RUNX2-II 以及基质金属蛋白酶 MMP1 和 MMP13 的表达相对年龄匹配的对照组降低,尽管成骨细胞标志物 BGLAP 没有明显改变。破骨细胞生成因子 RANKL 的表达降低,而抗破骨细胞生成因子骨保护素的表达增加。除了超氧化物歧化酶外,氧化应激标志物的表达变化通常不明显。这些数据表明氟化物对成骨细胞和破骨细胞分化所需因子的表达以及成骨细胞产物(包括 MMP1 和胶原蛋白)的表达具有强烈的影响。重要的是,这些影响是在氧化应激标志物表达没有显著变化的情况下观察到的。研究结果为在全器官发育模型中氟骨症的发生机制提供了第一个分子见解。