Ronco P, Allegri L, Brianti E, Chatelet F, Van Leer E H, Verroust P
INSERM U.64, Hôpital Tenon, Paris, France.
Appl Pathol. 1989;7(2):85-98.
Although membranous glomerulonephritis (MGN) has been long considered as a prototype of glomerulonephritis (GN) due to the deposition of circulating immune complexes (CIC), a growing body of evidence indicates that immune deposits can also be formed in situ and implicate antigens expressed by glomerular epithelial cells (GEC). Some of these antigens have recently been identified. The first one, gp330 - a 330-kd glycoprotein restricted to the coated pits of GEC and renal brush border (BB) - is responsible for Heymann nephritis, a rat model of MGN. However, it is absent in the human glomerulus and is therefore probably not involved in human cases of MGN, at least in those due to in situ formation of CIC. In addition, by raising monoclonal antibodies against rat and rabbit BB, we have isolated two other BB proteins also expressed on GEC. The latter, respectively identified as dipeptidyl peptidase IV (90 kd) and enkephalinase (85 kd), can serve as targets for the formation of short-lived immune deposits. Since they are also detected on human GEC, they might play a role in the pathogenesis of MGN in man.
尽管膜性肾小球肾炎(MGN)长期以来因循环免疫复合物(CIC)沉积而被视为肾小球肾炎(GN)的典型代表,但越来越多的证据表明,免疫沉积物也可在原位形成,并与肾小球上皮细胞(GEC)表达的抗原有关。其中一些抗原最近已被鉴定出来。第一种是gp330——一种330kd的糖蛋白,仅存在于GEC的被覆小窝和肾刷状缘(BB)——是Heymann肾炎(MGN的大鼠模型)的病因。然而,它在人类肾小球中不存在,因此可能不参与人类MGN病例,至少不参与那些因CIC原位形成导致的病例。此外,通过制备针对大鼠和兔BB的单克隆抗体,我们分离出了另外两种也在GEC上表达的BB蛋白。后者分别被鉴定为二肽基肽酶IV(90kd)和脑啡肽酶(85kd),可作为短暂免疫沉积物形成的靶点。由于它们也在人类GEC上被检测到,它们可能在人类MGN的发病机制中起作用。