van den Born J, van Kraats A A, Bakker M A, Assmann K J, Dijkman H B, van der Laak J A, Berden J H
Department of Nephrology, University Hospital St. Radboud, Nijmegen, The Netherlands.
Diabetologia. 1995 Oct;38(10):1169-75. doi: 10.1007/BF00422365.
Heparan sulphate-associated anionic sites in the glomerular basement membrane were studied in rats 8 months after induction of diabetes by streptozotocin and in age- adn sex-matched control rats, employing the cationic dye cuprolinic blue. Morphometric analysis at the ultrastructural level was performed using a computerized image processor. The heparan sulphate specificity of the cuprolinic blue staining was demonstrated by glycosaminoglycan-degrading enzymes, showing that pretreatment of the sections with heparitinase abolished all staining, whereas chondroitinase ABC had no effect. The majority of anionic sites (74% in diabetic and 81% in control rats) were found within the lamina rara externa of the glomerular basement membrane. A minority of anionic sites were scattered throughout the lamina densa and lamina rara interna, and were significantly smaller than those in the lamina rara externa of the glomerular basement membrane (p<0.001 and p<0.01 for diabetic and control rats, respectively). Diabetic rats progressively developed albuminuria reaching 40.3 (32.2-62.0) mg/24 h after 8 months in contrast to the control animals (0.8 (0.2-0.9) mg/24 h, p<0.002). At the same time, the number of heparan sulphate anionic sites and the total anionic site surface (number of anionic sites x mean anionic site surface) in the lamina rara externa of the glomerular basement membrane was reduced by 19% (p<0.021) and by 26% (p<0.02), respectively. Number and total anionic site surface in the remaining part of the glomerular basement membrane (lamina densa and lamina rara interna) were not significantly changed. We conclude that in streptozotocin-diabetic rats with an increased urinary albumin excretion, a reduced heparan sulphate charge barrier/density is found at the lamina rara externa of the glomerular basement membrane.
采用阳离子染料铜叶绿酸蓝,对链脲佐菌素诱导糖尿病8个月的大鼠以及年龄和性别匹配的对照大鼠肾小球基底膜中硫酸乙酰肝素相关阴离子位点进行了研究。使用计算机图像处理器在超微结构水平上进行形态计量分析。糖胺聚糖降解酶证实了铜叶绿酸蓝染色的硫酸乙酰肝素特异性,表明用乙酰肝素酶预处理切片可消除所有染色,而软骨素酶ABC则无影响。大多数阴离子位点(糖尿病大鼠中为74%,对照大鼠中为81%)位于肾小球基底膜的外疏松层内。少数阴离子位点散布于致密层和内疏松层,且明显小于肾小球基底膜外疏松层中的位点(糖尿病大鼠和对照大鼠分别为p<0.001和p<0.01)。与对照动物(0.8(0.2 - 0.9)mg/24 h,p<0.002)相比,糖尿病大鼠逐渐出现蛋白尿,8个月后达到40.3(32.2 - 62.0)mg/24 h。与此同时,肾小球基底膜外疏松层中硫酸乙酰肝素阴离子位点的数量和阴离子位点总面积(阴离子位点数量×平均阴离子位点面积)分别减少了19%(p<0.021)和26%(p<0.02)。肾小球基底膜其余部分(致密层和内疏松层)的位点数量和阴离子位点总面积无显著变化。我们得出结论,在尿白蛋白排泄增加的链脲佐菌素诱导糖尿病大鼠中,肾小球基底膜外疏松层存在硫酸乙酰肝素电荷屏障/密度降低的情况。