Kriz Wilhelm
Institut für Anatomie und Zellbiologie, Universität Heidelberg, D-69120 Heidelberg, Germany.
Microsc Res Tech. 2002 May 15;57(4):189-95. doi: 10.1002/jemt.10072.
The concept that the podocyte is the major culprit underlying development and progression of glomerular diseases leading to chronic renal failure is well established. The essential steps in this process are (1) the establishment of tuft adhesions to Bowman's capsule; (2) the formation by capillaries contained in a tuft adhesion of a filtrate that is delivered, instead into Bowman's space, towards the interstitium; and (3) the spreading of this filtrate on the outer aspect of the affected nephron leading to the degeneration of this nephron. The present review summarizes the pros and cons concerning the relevance of misdirected filtration for a nephron-to-nephron transfer of the disease at the level of the tubular interstitium. Surprisingly, the histopathology clearly shows that interstitial proliferation surrounding degenerating nephrons tends to encapsulate the degenerative process, confining it to the already affected nephron. No evidence is available that the disease, mediated by interstitial proliferation and matrix deposition, may jump to a neighboring, so far unaffected, nephron. It appears that the process that leads to the degeneration of a nephron in the context of "classic" FSGS always starts separately in the respective glomerulus by severe podocyte injury.
足细胞是导致慢性肾衰竭的肾小球疾病发生和进展的主要罪魁祸首,这一概念已得到充分确立。这一过程的关键步骤包括:(1)肾小球与鲍曼囊建立粘连;(2)粘连的肾小球毛细血管形成滤液,该滤液不是进入鲍曼腔,而是朝向间质;(3)这种滤液在受影响肾单位的外侧扩散,导致该肾单位退化。本综述总结了关于错误导向的滤过在肾小管间质水平上疾病从一个肾单位转移到另一个肾单位的相关性的利弊。令人惊讶的是,组织病理学清楚地表明,围绕退化肾单位的间质增生倾向于包裹退化过程,将其局限于已经受影响的肾单位。没有证据表明由间质增生和基质沉积介导的疾病会转移到相邻的、迄今为止未受影响的肾单位。在“经典”局灶节段性肾小球硬化症(FSGS)背景下导致肾单位退化的过程似乎总是由严重的足细胞损伤在各自的肾小球中单独启动。