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首页> 外文期刊>International Journal of Molecular Sciences >iTRAQ-Based Proteomics Analysis of Serum Proteins in Wistar Rats Treated with Sodium Fluoride: Insight into the Potential Mechanism and Candidate Biomarkers of Fluorosis
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iTRAQ-Based Proteomics Analysis of Serum Proteins in Wistar Rats Treated with Sodium Fluoride: Insight into the Potential Mechanism and Candidate Biomarkers of Fluorosis

机译:基于iTRAQ的氟化钠处理的Wistar大鼠血清蛋白的蛋白质组学分析:氟中毒的潜在机制和候选生物标志物的见解

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Fluorosis induced by exposure to high level fluoride is quite widespread in the world. The manifestations of fluorosis include dental mottling, bone damage, and impaired malfunction of soft tissues. However, the molecular mechanism of fluorosis has not been clarified until now. To explore the underlying mechanisms of fluorosis and screen out serum biomarkers, we carried out a quantitative proteomics study to identify differentially expressed serum proteins in Wistar rats treated with sodium fluoride (NaF) by using a proteomics approach of isobaric tagging for relative and absolute quantitation (iTRAQ). We fed Wistar rats drinking water that had 50, 150, and 250 mg/L of dissolved NaF for 24 weeks. For the experimental duration, each rat was given an examination of the lower incisors to check for the condition of dental fluorosis (DF). By the end of the treatment, fluoride ion concentration in serum and lower incisors were detected. The results showed that NaF treatment can induce rat fluorosis. By iTRAQ analysis, a total of 37 differentially expressed serum proteins were identified between NaF-treated and control rats. These proteins were further analyzed by bioinformatics, out of which two proteins were validated by enzyme-linked immunoadsorbent assays (ELISA). The major proteins were involved in complement and coagulation cascade, inflammatory response, complement activation, defense response, and wound response, suggesting that inflammation and immune reactions may play a key role in fluorosis pathogenesis. These proteins may contribute to the understanding of the mechanism of fluoride toxicity, and may serve as potential biomarkers for fluorosis.
机译:暴露于高水平氟化物引起的氟中毒在世界范围内相当普遍。氟中毒的表现包括牙齿斑点,骨骼损伤和软组织功能障碍。然而,氟中毒的分子机制至今尚未阐明。为了探索氟中毒的潜在机制并筛选出血清生物标志物,我们进行了定量蛋白质组学研究,通过使用等压标记的蛋白质组学方法相对和绝对定量来鉴定氟化钠(NaF)处理的Wistar大鼠中差异表达的血清蛋白( iTRAQ)。我们给Wistar大鼠喂食了溶解有50、150和250 mg / L NaF的饮用水,持续24周。在实验期间,对每只大鼠的下门牙进行检查,以检查其氟牙症(DF)的状况。治疗结束时,检测到血清和下门牙中的氟离子浓度。结果表明,NaF处理可诱发大鼠氟中毒。通过iTRAQ分析,在经NaF处理的大鼠和对照大鼠之间共鉴定出37种差异表达的血清蛋白。这些蛋白质通过生物信息学进一步分析,其中两个蛋白质通过酶联免疫吸附测定(ELISA)进行了验证。主要蛋白质参与补体和凝血级联,炎症反应,补体激活,防御反应和伤口反应,提示炎症和免疫反应可能在氟中毒发病中起关键作用。这些蛋白质可能有助于理解氟化物毒性的机制,并可以作为潜在的氟中毒生物标志物。

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