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芬兰型先天性肾病综合征中的肾小球阴离子电荷

Glomerular anionic charge in congenital nephrotic syndrome of the Finnish type.

作者信息

Ljungberg P, Rapola J, Holmberg C, Holthöfer H, Jalanko H

机构信息

Department of Bacteriology and Immunology, University of Helsinki, Finland.

出版信息

Histochem J. 1995 Jul;27(7):536-46.

PMID:7591846
Abstract

Decrease of the anionic charge of the glomerular basement membrane and especially the reduced amount of heparan sulphate proteoglycan in the lamina rara externa has been suggested to be the basic pathogenetic defect in congenital nephrotic syndrome. In the present study the anionic charge of glomeruli was examined in the congenital nephrotic syndrome of the Finnish type and in controls using cationic stains (polyethyleneimine, Ruthenium Red) in electron microscopy. Chondroitinase and heparinase treatments were used to characterize further the anionic elements detected. Scanning electron microscopy (SEM) was used in addition to transmission electron microscopy (TEM) to examine the tridimensional structure and secondary changes of podocytes in this syndrome. The number (mean +/- SD) of polyethyleneimine granules per 1 micron length of lamina rara externa of the glomerular basement membrane was 24.9 +/- 4.5 in control and 23.2 +/- 4.3 [corrected] in congenital nephrotic syndrome subjects. The Ruthenium Red staining pattern was closely similar in syndrome and control kidneys. The granules evident after staining with either cationic stain were seen after chondroitinase but not after heparinase treatment in control as well as in syndrome patient kidney samples. No denuded areas of basement membrane in 42 glomeruli from four syndrome patients were found in SEM. In conclusion, the amount of anionic sites in the lamina rara externa as detected by either cationic stain was comparable to controls. These results do not support the hypothesis of decreased anionic sites in the lamina rara externa of the glomerular basement membrane in congenital nephrotic syndrome of the Finnish type.

摘要

肾小球基底膜阴离子电荷的减少,尤其是肾小球基底膜外侧稀疏层硫酸乙酰肝素蛋白聚糖数量的减少,被认为是先天性肾病综合征的基本发病机制缺陷。在本研究中,使用阳离子染料(聚乙烯亚胺、钌红)通过电子显微镜检查了芬兰型先天性肾病综合征患者及对照者肾小球的阴离子电荷。采用软骨素酶和肝素酶处理进一步表征所检测到的阴离子成分。除了透射电子显微镜(TEM)外,还使用扫描电子显微镜(SEM)检查该综合征中足细胞的三维结构和继发性变化。肾小球基底膜外侧稀疏层每1微米长度的聚乙烯亚胺颗粒数量(平均值±标准差)在对照组中为24.9±4.5,在先天性肾病综合征患者中为23.2±4.3[校正后]。钌红染色模式在综合征患者和对照者的肾脏中非常相似。在对照者以及综合征患者的肾脏样本中,用任何一种阳离子染料染色后可见的颗粒在软骨素酶处理后可见,但在肝素酶处理后不可见。在扫描电子显微镜下,未在4例综合征患者的42个肾小球中发现基底膜剥脱区域。总之,通过任何一种阳离子染料检测到的肾小球基底膜外侧稀疏层阴离子位点数量与对照者相当。这些结果不支持芬兰型先天性肾病综合征患者肾小球基底膜外侧稀疏层阴离子位点减少的假说。

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本文引用的文献

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Congenital nephrotic syndrome.
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Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish type.芬兰型先天性肾病综合征的移植后肾病
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Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.芬兰型先天性肾病综合征定位于19号染色体长臂。
Am J Hum Genet. 1994 May;54(5):757-64.
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Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type.
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Glycosaminoglycans in urine and amniotic fluid in congenital nephrotic syndrome of the Finnish type.芬兰型先天性肾病综合征患者尿液和羊水中的糖胺聚糖
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Management of congenital nephrotic syndrome of the Finnish type.芬兰型先天性肾病综合征的管理
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Congenital nephrosis of the Finnish type (CNF): matrix components of the glomerular basement membranes and of cultured mesangial cells.芬兰型先天性肾病(CNF):肾小球基底膜和培养的系膜细胞的基质成分。
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Ultrastructural alteration of glomerular anionic sites in nephrotic patients.肾病患者肾小球阴离子位点的超微结构改变
Pediatr Nephrol. 1993 Feb;7(1):1-5. doi: 10.1007/BF00861549.
9
Alterations in the charge and size selectivity barrier of the glomerular filter in aminonucleoside nephrosis in rats.大鼠氨基核苷肾病中肾小球滤过器电荷和大小选择性屏障的改变。
Lab Invest. 1981 Mar;44(3):271-9.
10
Detachment of endothelium and epithelium from the glomerular basement membrane produced by kidney perfusion with neuraminidase.用神经氨酸酶灌注肾脏导致内皮和上皮从肾小球基底膜分离。
Lab Invest. 1980 Mar;42(3):375-84.