Andrews P M
Am J Anat. 1981 Oct;162(2):89-106. doi: 10.1002/aja.1001620202.
The distribution and effects of polycationized ferritin (PCF) bound ot anionic sites on living plasmalemmas and basal laminae of normal and puromycin aminonucleoside nephrotic (PAN) kidneys were studied using an in vitro model system. Immersion of normal glomeruli in physiological saline solutions containing low concentrations of PCF (0.01 to 0.1 mg/ml) for 10 seconds results in preferential binding of PCF to microvillous projections on the glomerular epithelium (i.e., podocytes). Exposure to higher concentrations of PCF (1.0 mg/ml) for 10 seconds results in several layers of PCF distributed evenly over the urinary aspect of epithelial podocytes. In these short treatment times, the thin slit diaphragms which span the filtration slits appear to be impermeable to PCF. Within several minutes after PCF treatment, ferritin is found within caveolae on the surface of epithelial podocytes and within numerous pinosomes and larger endocytic vesicles within these cells. Longer treatment with PCF results in the narrowing of filtration slit spaces and the formation of junctions between adjacent podocyte foot processes. Occurringg coincident with these structural changes is a gradual accumulation of PCF in regular patches along the lamina rara externa (LRE) of the glomerular basement membrane. Loss of foot processes and accumulation of PCF in the LRE are prevented by treatment with either cytochalasin B (25 micro g/ml), D (2 micro g/ml) or incubation at low temperatures (0-4 degrees C). When PCF-coated glomeruli are incubated in PCF-free media, the ferritin coat is shed form the free surfaces within 1/2 to 1 hour except at the tips and sides of microvillous projections. Pretreatment of normal glomeruli with neuraminidase or protamine sulfate results in a dramatic reduction in the binding of PCF to the glomerular epithelial free surface. Treatment of PAN glomeruli with PCF often results in patchlike distributions of PCF over the glomerular epithelial free surface. High concentrations of PCF (1.0 mg/ml) bind preferentially to microvillous projections on the parietal epithelial luminal surface and in distinct patchlike patterns along the basal laminae of parietal and tubular epithelial cells.
利用体外模型系统,研究了结合于正常和嘌呤霉素氨基核苷肾病(PAN)肾活体质膜和基膜阴离子位点上的聚阳离子化铁蛋白(PCF)的分布及效应。将正常肾小球浸入含低浓度PCF(0.01至0.1毫克/毫升)的生理盐溶液中10秒钟,会导致PCF优先结合于肾小球上皮(即足细胞)的微绒毛突起上。暴露于较高浓度的PCF(1.0毫克/毫升)10秒钟,会使多层PCF均匀分布于上皮足细胞的尿侧。在这些短时间处理中,横跨滤过裂隙的薄裂孔隔膜似乎对PCF不可渗透。PCF处理后几分钟内,铁蛋白出现在上皮足细胞表面的小窝内以及这些细胞内众多的胞饮小体和较大的内吞小泡内。用PCF进行更长时间的处理会导致滤过裂隙空间变窄以及相邻足细胞足突之间形成连接。与这些结构变化同时发生的是,PCF沿着肾小球基底膜的外疏松层(LRE)以规则斑块的形式逐渐积累。用细胞松弛素B(25微克/毫升)、D(2微克/毫升)处理或在低温(0 - 4摄氏度)下孵育可防止足突丢失和PCF在LRE中的积累。当用PCF包被的肾小球在不含PCF的培养基中孵育时,除了微绒毛突起的尖端和侧面外,铁蛋白包被在1/2至1小时内从自由表面脱落。用神经氨酸酶或硫酸鱼精蛋白预处理正常肾小球会导致PCF与肾小球上皮自由表面的结合显著减少。用PCF处理PAN肾小球通常会导致PCF在肾小球上皮自由表面呈斑块状分布。高浓度的PCF(1.0毫克/毫升)优先结合于壁层上皮腔表面的微绒毛突起以及沿着壁层和肾小管上皮细胞基膜的明显斑块状区域。