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小鼠抗肾小球基底膜肾炎:异源期严重蛋白尿

Anti-GBM nephritis in the mouse: severe proteinuria in the heterologous phase.

作者信息

Assmann K J, Tangelder M M, Lange W P, Schrijver G, Koene R A

出版信息

Virchows Arch A Pathol Anat Histopathol. 1985;406(3):285-99. doi: 10.1007/BF00704298.

Abstract

Highly reproducible anti glomerular basement membrane (GBM) nephritis has been induced in the mouse after a single injection of rabbit or goat antibody against purified homologous GBM. The severity of albuminuria was closely related to the amount of antibody given. With doses of 4 mg or more, low serum albumin concentrations, sometimes accompanied by ascites and oedema, were observed after 1 week. Glomerular injury was characterized by an initial accumulation of polymorphonuclear granulocytes followed by thrombosis and necrosis, the extent of which defined the outcome of the glomerulonephritis. With high doses of antibody the exudative lesions entered a chronic phase, while at doses lower than 2 mg remission of the lesions occurred. Immunofluorescence studies showed prompt linear fixation of the injected antibodies to the glomerular capillary wall, accompanied by immediate binding of C3 in a fine granular pattern. Fibrin deposits appeared at 2 h in some glomeruli, increased thereafter, and were present after one day in more than 90% of the glomeruli in mice that had received 4 mg of antibody. This new reproducible model in the mouse is suited for the study of the relationship between activation of mediator systems, histological lesions, and proteinuria.

摘要

单次注射兔或山羊抗纯化同源肾小球基底膜(GBM)抗体后,可在小鼠中诱导出高度可重复的抗GBM肾炎。蛋白尿的严重程度与给予的抗体量密切相关。给予4毫克或更多剂量时,1周后观察到血清白蛋白浓度降低,有时伴有腹水和水肿。肾小球损伤的特征是多形核粒细胞最初积聚,随后出现血栓形成和坏死,其程度决定了肾小球肾炎的结局。给予高剂量抗体时,渗出性病变进入慢性期,而给予低于2毫克剂量时,病变会缓解。免疫荧光研究显示,注射的抗体迅速以线性方式固定在肾小球毛细血管壁上,同时C3以细颗粒模式立即结合。在一些肾小球中,2小时出现纤维蛋白沉积,此后增加,在接受4毫克抗体的小鼠中,一天后超过90%的肾小球中存在纤维蛋白沉积。这种新的小鼠可重复模型适用于研究介质系统激活、组织学病变和蛋白尿之间的关系。

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