Kawachi H, Kurihara H, Topham P S, Brown D, Shia M A, Orikasa M, Shimizu F, Salant D J
Evans Memorial Department of Clinical Research, Boston University Medical Center, Massachusetts 02118, USA.
Am J Physiol. 1997 Dec;273(6):F984-93. doi: 10.1152/ajprenal.1997.273.6.F984.
Monoclonal antibody (MAb) 5-1-6 identifies a 51-kDa protein (p51) on rat podocyte foot processes and causes severe complement- and leukocyte-independent proteinuria when injected into rats. In the studies reported here, we used various immunohistological techniques to define the precise location of p51 and its relationship to ZO-1, a known component of the podocyte slit diaphragm in adult rat glomeruli. Our results demonstrate that p51 and ZO-1 lie close to each other on opposite sides of the podocyte plasma membrane at the point of insertion of the slit diaphragm: ZO-1 on the cytoplasmic face and p51 on the slit diaphragm and adjoining outer leaflet of the plasma membrane bordering the filtration slits. In addition to their geographic proximity, there appears to be a relationship between p51 and ZO-1. After MAb 5-1-6 injection, there was a progressive decline in stainable ZO-1 in the podocytes of heavily proteinuric rats. In addition, Western blot analysis of glomerular lysates showed that the decline in staining was due to a loss of immunoreactive ZO-1 rather than redistribution or diffusion of the protein. Simultaneously, the distribution of glomerular-bound MAb 5-1-6 became more clumped, apparently because of partial endocytosis into a lysosomal compartment, while the slit diaphragms remained morphologically intact. These findings suggest that MAb 5-1-6 alters the molecular composition of the slit diaphragm and thereby affects the glomerular permeability barrier.
单克隆抗体(MAb)5-1-6可识别大鼠足细胞足突上的一种51 kDa蛋白(p51),将其注入大鼠体内会导致严重的不依赖补体和白细胞的蛋白尿。在本文报道的研究中,我们使用了各种免疫组织学技术来确定p51的精确位置及其与ZO-1的关系,ZO-1是成年大鼠肾小球足细胞裂孔隔膜的已知组成成分。我们的结果表明,在裂孔隔膜插入点处,p51和ZO-1在足细胞质膜的相对两侧彼此靠近:ZO-1位于细胞质面,p51位于裂孔隔膜以及与滤过裂隙相邻的质膜外小叶上。除了在空间位置上接近外,p51和ZO-1之间似乎还存在某种关系。注射MAb 5-1-6后,重度蛋白尿大鼠足细胞中可染色的ZO-1逐渐减少。此外,肾小球裂解物的蛋白质印迹分析表明,染色减少是由于免疫反应性ZO-1的丢失,而非该蛋白的重新分布或扩散。同时,肾小球结合的MAb 5-1-6的分布变得更加聚集,这显然是因为部分被内吞到溶酶体区室,而裂孔隔膜在形态上保持完整。这些发现表明,MAb 5-1-6改变了裂孔隔膜的分子组成,从而影响了肾小球滤过屏障。