Kunz A, Brown D, Vassalli J D, Kontturi M, Kumpulainen T, Orci L
Lab Invest. 1985 Oct;53(4):413-20.
The lectin-gold technique was used to reveal Helix pomatia lectin (HPL)-binding sites in human kidney glomeruli. HPL-binding sites were associated mainly with podocyte foot process bases, and extended over the lamina rara externa of the glomerular basement membrane. In addition, kidneys from blood group A1 donors showed labeling of capillary endothelial cells and erythrocytes. After neuraminidase digestion of the sections prior to incubation with HPL-gold complexes, HPL-binding sites appeared on previously negative regions of the glomerulus. This increase in labeling was particularly striking at the level of the podocyte-free surface (adjacent to the urinary space) in all kidneys, and on capillary endothelial cells from donors of blood groups other than A1. These results demonstrate the existence of two distinct glycocalyx domains in human kidney podocytes, and show the application of the lectin-gold technique for the high resolution, ultrastructural detection and quantification of lectin-binding sites in human material.
采用凝集素-金技术揭示人肾小球中苹果蜗牛凝集素(HPL)的结合位点。HPL结合位点主要与足细胞足突基部相关,并延伸至肾小球基底膜的外疏松层。此外,A1血型供体的肾脏显示毛细血管内皮细胞和红细胞有标记。在用HPL-金复合物孵育之前对切片进行神经氨酸酶消化后,HPL结合位点出现在肾小球先前阴性的区域。这种标记增加在所有肾脏的无足细胞表面(与尿腔相邻)水平尤为显著,在非A1血型供体的毛细血管内皮细胞上也很明显。这些结果证明了人肾足细胞中存在两个不同的糖萼结构域,并展示了凝集素-金技术在高分辨率超微结构检测和定量人材料中凝集素结合位点方面的应用。