Silva F G, Hoyer J R, Pirani C L
Lab Invest. 1984 Oct;51(4):404-15.
Injection of presensitized rats with goat antiserum to rat glomerular basement membrane (GBM) results in a crescentic glomerulonephritis with typical linear deposition of goat IgG and host IgG and C3 along the GBM. Sequential renal biopsies from rats with this model of anti-GBM nephritis were studied by light, electron, and immunofluorescence microscopy to investigate the mechanisms of crescent formation. The localization of fibrin-related antigens (FRA) and factor VIII-related antigens (VIIIAGN) at different stages of disease was specifically studied since earlier studies of human glomerulonephritis had shown deposits of FRA without VIIIAGN in crescents and suggested that either a thrombin-independent mechanism might cause fibrin deposition or, alternatively, that glomerular fibrinolysis was relatively deficient within Bowman's space. Separation of the endothelium from the GBM or glomerular endothelial loss was the first change noted, a lesion that promotes intracapillary FRA deposition. Subsequently, intracapillary hypercellularity and GBM damage became progressively more severe. During the second and third weeks, coincident with early crescent formation, increasing amounts of FRA were noted within Bowman's space; FRA in crescents persisted throughout the study, whereas FRA within the glomerular tuft decreased over time. In early lesions, granular deposits of IgM and factor VIIIAGN were found diffusely within crescents. However, at later times, extracapillary deposits of these proteins and IgG were limited to the periphery of crescents within the markedly thickened and altered Bowman's capsule. Persistence of IgM and factor VIIIAGN at the periphery of older crescents appears to result from entrapment in areas less subject to cellular degradation and transport. Preferential clearance of FRA from the glomerular tuft suggests that fibrinolysis is less effective in Bowman's space than clearance mechanisms within glomerular capillaries.
给预先致敏的大鼠注射抗大鼠肾小球基底膜(GBM)山羊抗血清,会导致新月体性肾小球肾炎,山羊IgG、宿主IgG和C3沿GBM呈典型的线性沉积。通过光镜、电镜和免疫荧光显微镜对患有这种抗GBM肾炎模型的大鼠进行连续肾活检,以研究新月体形成的机制。由于早期对人类肾小球肾炎的研究显示新月体中有纤维蛋白相关抗原(FRA)沉积但无VIII相关抗原(VIIIAGN),并提示要么是一种不依赖凝血酶的机制可能导致纤维蛋白沉积,要么是肾小球内纤维蛋白溶解在鲍曼囊内相对不足,因此专门研究了疾病不同阶段纤维蛋白相关抗原(FRA)和VIII相关抗原(VIIIAGN)的定位。内皮与GBM分离或肾小球内皮丢失是首先观察到的变化,这是一种促进毛细血管内FRA沉积的病变。随后,毛细血管内细胞增多和GBM损伤逐渐加重。在第二和第三周,与早期新月体形成同时,鲍曼囊内FRA的量逐渐增加;整个研究过程中新月体内的FRA持续存在,而肾小球丛内的FRA随时间减少。在早期病变中,IgM和VIIIAGN的颗粒状沉积物在新月体内弥漫性存在。然而,在后期,这些蛋白质和IgG的毛细血管外沉积物仅限于明显增厚和改变的鲍曼囊内新月体的周边。较老新月体周边IgM和VIIIAGN的持续存在似乎是由于被困在细胞降解和转运较少的区域。肾小球丛中FRA的优先清除表明,纤维蛋白溶解在鲍曼囊内比在肾小球毛细血管内的清除机制效率更低。