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首页> 外文期刊>BMC Immunology >Lupus-like oral mucosal lesions in mercury-induced autoimmune response in Brown Norway rats
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Lupus-like oral mucosal lesions in mercury-induced autoimmune response in Brown Norway rats

机译:褐斑狼疮样口腔黏膜病变对水银诱导的挪威褐鼠的自身免疫反应

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Background Administration of mercury at nontoxic doses induces systemic autoimmune disease in Brown Norway (BN) rats. The pathogenesis of lupus-like oral mucosal lesion by mercury-induced autoimmunity is still unclear, even though the oral mucosa is observed to be commonly affected in mercury-treated BN rats. In this study, we investigated the immunopathology of lupus-like oral mucosal lesions in a model of mercury-induced systemic autoimmunity. Methods Brown Norway male rats were injected subcutaneously with either phosphate-buffered saline (control) or mercury at a dose of 1.0 mg per kilogram of body weight on days 0, 3, 5, and 7. Blood, kidney, and tongue samples were taken at various timepoints for evaluation by immunohistochemistry, RT-PCR, and lupus band test (LBT). Results Oral mucosal lesions were classified according to three consecutive temporal phases on the basis of infiltration of immunocompetent cells as follows: (phase I) infiltration of MHC class II+ dendritic cells (DC) and macrophages; (phase II) addition of ED1+ macrophage infiltrates; and (phase III) focal infiltration of pan T cells following increased infiltration of DC and macrophages. Dense infiltration of DC and macrophages was observed in the basement membrane (BM) zone of the oral epithelium. Tissue expression of IL-4 mRNA was detected in early lesions (phase I), suggesting that locally produced IL-4 may be responsible for Th2-mediated immune response. A linear and continuous smooth pattern of fluorescence was observed in the oral epithelial BM in addition to renal glomeruli, indicating immune complex deposits. Conclusions Local autoimmune responses are involved in the pathogenesis of mercury-induced lupus-like lesions of the oral mucosa.
机译:背景技术以无毒剂量施用汞可诱发褐挪威(BN)大鼠系统性自身免疫病。汞诱导的自身免疫性狼疮样口腔粘膜病变的发病机制仍不清楚,即使观察到口腔粘膜通常在汞治疗的BN大鼠中受到影响。在这项研究中,我们调查了汞诱导的全身自身免疫模型中狼疮样口腔粘膜病变的免疫病理学。方法在第0、3、5和7天,皮下注射挪威磷酸盐处理的雄性大鼠皮下注射磷酸盐缓冲盐水(对照)或汞,剂量为每千克体重1.0 mg。采集血液,肾脏和舌头样本在各个时间点进行免疫组织化学,RT-PCR和狼疮谱带试验(LBT)评估。结果根据免疫功能细胞的浸润,将口腔粘膜病变分为三个连续的时间阶段:(I期)MHC II类sup树突状细胞(DC)和巨噬细胞浸润; (阶段II)添加ED1 + 巨噬细胞浸润; DC和巨噬细胞浸润增加后,泛T细胞的局部浸润(第三阶段)。在口腔上皮的基底膜(BM)区观察到DC和巨噬细胞的密集浸润。在早期病变(I期)中检测到IL-4 mRNA的组织表达,这表明本地产生的IL-4可能是Th2介导的免疫反应的原因。除肾小球外,在口腔上皮BM中还观察到了线性且连续的平滑荧光模式,表明存在免疫复合物沉积。结论局部自身免疫反应与汞诱导的口腔粘膜狼疮样病变的发病机制有关。

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