GLOMERULAR ANIONIC CHARGE IN CONGENITAL NEPHROTIC SYNDROME OF THE FINNISH TYPE

被引:0
作者
LJUNGBERG, P
RAPOLA, J
HOLMBERG, C
HOLTHOFER, H
JALANKO, H
机构
[1] HELSINKI UNIV,DEPT PATHOL,SF-00014 HELSINKI,FINLAND
[2] HELSINKI UNIV,CHILDRENS HOSP,SF-00014 HELSINKI,FINLAND
来源
HISTOCHEMICAL JOURNAL | 1995年 / 27卷 / 07期
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 mu m length of lamina rara externa of the glomerular basement membrane was 24.9 +/- 4.5 in control and 2.32 +/- 4.3 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.
引用
收藏
页码:536 / 546
页数:11
相关论文
共 47 条
[1]  
ARAKAWA M, 1970, LAB INVEST, V23, P489
[2]   SCANNING ELECTRON-MICROSCOPIC STUDY OF NORMAL HUMAN GLOMERULOGENESIS AND OF FETAL GLOMERULI IN CONGENITAL NEPHROTIC SYNDROME OF THE FINNISH TYPE [J].
AUTIOHARMAINEN, H ;
VAANANEN, R ;
RAPOLA, J .
KIDNEY INTERNATIONAL, 1981, 20 (06) :747-752
[3]  
BARSOTTI P, 1988, J SUBMICR CYTOL PATH, V20, P549
[4]   AFFINITY CYTOCHEMICAL LABELING OF GLOMERULAR-BASEMENT-MEMBRANE ANIONIC SITES USING SPECIFIC BIOTINYLATION AND COLLOIDAL GOLD PROBES [J].
BERTOLATUS, JA .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1990, 38 (03) :377-384
[5]   GLOMERULAR SIEVING OF ANIONIC AND NEUTRAL BOVINE ALBUMINS IN PROTEINURIC RATS [J].
BERTOLATUS, JA ;
HUNSICKER, LG .
KIDNEY INTERNATIONAL, 1985, 28 (03) :467-476
[6]  
BLOOM PM, 1959, ANAT REC, V133, P251
[7]   LOCALIZATION OF HEPARAN-SULFATE PROTEOGLYCAN IN BASEMENT-MEMBRANE BY SIDE-CHAIN STAINING WITH CUPROLINIC BLUE AS COMPARED WITH CORE PROTEIN LABELING WITH IMMUNOGOLD [J].
CHAN, FL ;
INOUE, S ;
LEBLOND, CP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (10) :1559-1572
[8]   CHANGES IN HEPARAN-SULFATE CORRELATE WITH INCREASED GLOMERULAR-PERMEABILITY [J].
GROGGEL, GC ;
STEVENSON, J ;
HOVINGH, P ;
LINKER, A ;
BORDER, WA .
KIDNEY INTERNATIONAL, 1988, 33 (02) :517-523
[9]  
GROGGEL GC, 1987, AM J PATHOL, V128, P521
[10]   CONGENITAL NEPHROTIC SYNDROME [J].
HALLMAN, N ;
HJELT, L .
JOURNAL OF PEDIATRICS, 1959, 55 (02) :152-162