Andres G A, Szymanski C, Albini B, Brentjens J, Milgrom M, Noble B, Ossi E, Steblay R
Am J Pathol. 1979 Jul;96(1):21-34.
In order to analyze the role of phagocytic cells in experimental antitubular basement membrane (TBM) antibody-mediated nephritis, Hartley guinea pigs (GP) were immunized with rabbit tubular basement membrane (TBM) in complete Freund's adjuvant and pertussis vaccine. Renal tissue was obtained 10 to 15, 15 to 25, and 25 to 35 days after the start of immunization. Severe renal tubulointerstitial (RTI) nephritis developed in 95% of the animals. Linear deposits of IgG and C3 along TBM were seen 10 days after initial immunization. A few days later, monocytes and macrophages infiltrated the interstitium and subsequently differentiated into epithelioid and foreign body-type giant cells (GC). The GC were most actively involved in the destruction of the TBM: Cytoplasmic pseudopodia of the GC adhered to the TBM; the areas of membrane apposition were several microns in length; no evidence of specialization was found in the plasma membrane adjoining the TBM; no cellular organelles, except for abundant microfilaments, were seen in the contact regions. The initial contact was followed by lysis of plasma membrane of the GC and TBM, perforation of TBM, and phagocytosis of TBM fragments. Concomitantly, fluorescent staining for IgG along the TBM became discontinuous or disappeared. Destruction of TBM was accompanied by degeneration of tubular epithelial cells and collapse of tubular architecture. The morphologic observations are consistent with the hypothesis that, in GP, autoimmune RTI nephritis damage of TBM results from the cooperation of humoral and cellular mechanisms, probably akin to those of antibody-mediated lymphocytotoxicity.
为了分析吞噬细胞在实验性抗肾小管基底膜(TBM)抗体介导的肾炎中的作用,将Hartley豚鼠(GP)用兔肾小管基底膜(TBM)与完全弗氏佐剂及百日咳疫苗一起免疫。在免疫开始后的10至15天、15至25天和25至35天获取肾组织。95%的动物发生了严重的肾小管间质(RTI)肾炎。初次免疫10天后可见IgG和C3沿TBM呈线性沉积。几天后,单核细胞和巨噬细胞浸润间质,随后分化为上皮样和异物型巨细胞(GC)。GC最积极地参与TBM的破坏:GC的细胞质伪足附着于TBM;膜附着区域长度为几微米;在与TBM相邻的质膜中未发现特化迹象;在接触区域除了丰富的微丝外未见细胞器。最初的接触之后是GC和TBM的质膜溶解、TBM穿孔以及TBM片段的吞噬。同时,沿TBM的IgG荧光染色变得不连续或消失。TBM的破坏伴随着肾小管上皮细胞的变性和肾小管结构的塌陷。形态学观察结果与以下假说一致,即在GP中,TBM的自身免疫性RTI肾炎损伤是由体液和细胞机制共同作用导致的,可能类似于抗体介导的淋巴细胞毒性机制。