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氟对大鼠牙本质磷蛋白磷酸化的体内影响。

Altered phosphorylation of rat dentine phosphoproteins by fluoride in vivo.

作者信息

Milan A M, Waddington R J, Embery G

机构信息

Department of Basic Dental Science, Dental School, University of Wales College of Medicine, Heath Park, Cardiff, CF4 4XY, UK.

出版信息

Calcif Tissue Int. 1999 Mar;64(3):234-8. doi: 10.1007/s002239900609.

Abstract

Dentine phosphoproteins have been proposed to have an important role in mineralization. This study focused on the influence of fluoride on the biochemical composition of dentine phosphoproteins and attempts to relate changes to the altered mineralization witnessed during fluorosis. Wistar rats were rendered fluorotic by the administration of 20 ppm sodium fluoride in their drinking water ad libitum, a nonfluorotic group received double-distilled, deionized water only. After 17 weeks, the teeth showed signs of fluorosis. The incisors were removed, split longitudinally, and the pulps were removed. Teeth were powdered and demineralized in 10% EDTA with protease inhibitors, after which the organic matrix was extracted with 4 M guanidinium chloride. Phosphoproteins were selectively precipitated from the soluble extract by the addition of 1.0 M calcium chloride and further purified by anion exchange chromatography. SDS-PAGE revealed two protein bands with molecular weights of 130 kDa and 66 kDa in the nonfluorotic fraction and 116 kDa and 66 kDa in the fluorotic fraction. Western blotting analysis identified the 66 kDa band as alpha2-HS glycoprotein which co-precipitated with phosphoproteins. Electroelution of the protein bands was performed with subsequent biochemical analyses. Phosphate content was determined for each protein band and was detectable in the 116 kDa and 130 kDa bands from the fluorotic and nonfluorotic samples, respectively, with a decreased level noted in the 116 kDa band. The presence of phosphate and the amino acid analysis of these bands suggested their identity to be dentine phosphoproteins. No changes in the ratio of amino acids was detected in fluorotic samples. The fluoride-induced alterations to the biochemical structure of dentine phosphoproteins would appear to influence the phosphorylation of these macromolecules only, possibly affecting posttranslational events. Such alterations may play a role in disrupting the patterns of mineralization seen during fluorosis.

摘要

牙本质磷蛋白被认为在矿化过程中起重要作用。本研究聚焦于氟对牙本质磷蛋白生化组成的影响,并试图将这些变化与氟斑牙期间观察到的矿化改变联系起来。通过在饮水中随意给予20 ppm氟化钠使Wistar大鼠患氟斑牙,非氟斑牙组仅饮用双蒸去离子水。17周后,牙齿出现氟斑牙迹象。拔除切牙,纵向劈开,去除牙髓。将牙齿磨成粉末,在含有蛋白酶抑制剂的10%乙二胺四乙酸(EDTA)中脱矿,然后用4 M氯化胍提取有机基质。通过加入1.0 M氯化钙从可溶性提取物中选择性沉淀磷蛋白,并通过阴离子交换色谱进一步纯化。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)显示,非氟斑牙组分中有两条分子量分别为130 kDa和66 kDa的蛋白条带,氟斑牙组分中有116 kDa和66 kDa的蛋白条带。蛋白质印迹分析确定66 kDa条带为与磷蛋白共沉淀的α2-HS糖蛋白。对蛋白条带进行电洗脱并随后进行生化分析。测定每条蛋白条带的磷酸盐含量,在氟斑牙和非氟斑牙样品的116 kDa和130 kDa条带中分别可检测到,116 kDa条带中的含量有所降低。这些条带中磷酸盐的存在及其氨基酸分析表明它们是牙本质磷蛋白。在氟斑牙样品中未检测到氨基酸比例的变化。氟诱导的牙本质磷蛋白生化结构改变似乎仅影响这些大分子的磷酸化,可能影响翻译后事件。这种改变可能在破坏氟斑牙期间出现的矿化模式中起作用。

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