Whiteside C, Prutis K, Cameron R, Thompson J
Department of Medicine, University of Toronto, Canada.
Lab Invest. 1989 Dec;61(6):650-60.
To identify the structural change coincident with increased glomerular permeability in both adriamycin (ADR) and puromycin-aminonucleoside (PAN) nephrosis, we explored the temporal correlation between developing proteinuria, the reduction in glomerular polyanions, and the detachment of epithelium from glomerular basement membrane (GBM). Sprague-Dawley rats received a single tail-vein injection of PAN (150 mg/kg), ADR (7.5 mg/kg) or saline. Nephrotic-range proteinuria appeared between days 2 to 5 in the PAN-treated and days 5 to 10 in the ADR-treated rats. The GBM heparan sulfate charge density and epithelial membrane sialic acid (SA) content were determined before, during and after the rise in proteinuria. Polyethyleneimine was used to detect heparan sulfate and the number staining of renal cortical slices was used to detect heparin sulfate and the number of sites/microns GBM in the lamina rara externa were counted on electron micrographs (magnification x60,000). Controls had a regular distribution of polyethyleneimine 20.19 +/- 1.72 sites/microns (X + SD). In ADR rats, the polyethyleneimine density decreased by day 5, 18.61 +/- 1.79 sites/microns (p less than 0.05) which persisted to day 15, 17.38 +/- 1.27 sites/microns (p less than 0.02). PAN rats, by day 1, had significant reduction, 14.94 +/- 1.47 sites/microns (p less than 0.05), which persisted to day 20. The total membrane-bound SA content of isolated glomeruli was analyzed with a modified Warren's method. The SA content in control glomeruli was 46.8 +/- 8.0 nmol/mg glomerular protein (X +/- SD). In ADR rats, there was significant decrease in SA content to 84 +/- 3% of control (p less than 0.01) at day 15. In PAN rats, by day 2, the SA content was decreased to 73 +/- 18% of control (p less than 0.05). In both models, scanning and transmission electron microscopy revealed epithelial foot process fusion, loss of slit diaphragms, and vacuolization before increased proteinuria. Epithelial detachment from the GBM and rupture of vacuoles occurred coincidently with rapid development of nephrotic proteinuria in both models. In summary, reduced GBM heparan sulfate and epithelial SA content do not correlate with the onset of altered glomerular permeability, whereas epithelial detachment is coincident with the development of massive proteinuria in both ADR and PAN nephrosis.
为了确定阿霉素(ADR)和嘌呤霉素氨基核苷(PAN)肾病中与肾小球通透性增加同时发生的结构变化,我们探讨了蛋白尿形成、肾小球多阴离子减少以及上皮细胞与肾小球基底膜(GBM)分离之间的时间相关性。将Sprague-Dawley大鼠通过尾静脉单次注射PAN(150mg/kg)、ADR(7.5mg/kg)或生理盐水。PAN处理组大鼠在第2至5天出现肾病范围的蛋白尿,ADR处理组大鼠在第5至10天出现。在蛋白尿增加之前、期间和之后,测定GBM硫酸乙酰肝素电荷密度和上皮细胞膜唾液酸(SA)含量。使用聚乙烯亚胺检测硫酸乙酰肝素,并通过肾皮质切片的计数染色检测硫酸乙酰肝素,在电子显微镜(放大倍数×60,000)下计数外疏松层中每微米GBM的位点数量。对照组聚乙烯亚胺的分布规律,为20.19±1.72个位点/微米(X+SD)。在ADR大鼠中,到第5天时聚乙烯亚胺密度降低,为18.61±1.79个位点/微米(p<0.05),持续到第15天,为17.38±1.27个位点/微米(p<0.02)。PAN大鼠在第1天时显著降低,为14.94±1.47个位点/微米(p<0.05),持续到第20天。用改良的沃伦方法分析分离肾小球的总膜结合SA含量。对照肾小球中的SA含量为46.8±8.0nmol/mg肾小球蛋白(X±SD)。在ADR大鼠中,第15天时SA含量显著降低至对照的84±3%(p<0.01)。在PAN大鼠中,到第2天时,SA含量降低至对照的73±18%(p<0.05)。在两种模型中,扫描和透射电子显微镜均显示在蛋白尿增加之前上皮足突融合、裂孔隔膜丧失和空泡化。在两种模型中,上皮细胞与GBM分离以及空泡破裂与肾病性蛋白尿的快速发展同时发生。总之,GBM硫酸乙酰肝素减少和上皮SA含量降低与肾小球通透性改变的发生无关,而上皮细胞分离与ADR和PAN肾病中大量蛋白尿的发展同时发生。