A MONOCLONAL-ANTIBODY AGAINST GBM HEPARAN-SULFATE INDUCES AN ACUTE SELECTIVE PROTEINURIA IN RATS

被引:218
作者
VANDENBORN, J
VANDENHEUVEL, LPWJ
BAKKER, MAH
VEERKAMP, JH
ASSMANN, KJM
BERDEN, JHM
机构
[1] CATHOLIC UNIV NIJMEGEN,DEPT MED,DIV NEPHROL,NIJMEGEN,NETHERLANDS
[2] CATHOLIC UNIV NIJMEGEN,DEPT BIOCHEM,NIJMEGEN,NETHERLANDS
[3] CATHOLIC UNIV NIJMEGEN,DEPT PATHOL,NIJMEGEN,NETHERLANDS
关键词
D O I
10.1038/ki.1992.15
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
After immunization of mice with partially-purified heparan sulfate proteoglycan (HSPG) isolated from rat glomeruli, a monoclonal antibody (mAb JM-403) was obtained, which was directed against heparan sulfate (HS), the glycosaminoglycan side chain of HSPG. In ELISA it reacted with isolated human glomerular basement membrane (GBM) HSPG, HS and hyaluronic acid, but not with the core protein of human GBM HSPG, and not with chondroitin sulfate A and C, dermatan sulfate, keratan sulfate and heparin. Furthermore, it did not bind to laminin, collagen type IV or fibronectin. Specificity of JM-403 for HS was also suggested by results of inhibition studies, which found that intact HSPG and HS, but not the core protein, inhibited the binding of JM-403 to HS. In indirect immunofluorescence on cryostat sections of rat kidney, a fine granular to linear staining of the GBM was observed, along with a variable staining of the other renal basement membranes. Pretreatment of the sections with heparitinase completely prevented the binding of mAb JM-403, whereas pretreatment with chondroitinase ABC or hyaluronidase had no effect. The precise binding site of mAb JM-403 was investigated by indirect immunoelectron microscopy. It revealed a diffuse staining of the whole width of the GBM. One hour after intravenous injection of JM-403 into rats, the mAb was detected along the glomerular capillary wall in a fine granular pattern, which shifted towards a more mesangial localization after 24 hours. No binding was observed anymore by day 15. Intravenous injection induced a dose-dependent, transient and selective proteinuria that was maximal immediately after the injection. Administration of 2 mg of JM-403 increased the urinary albumin excretion within the first 24 hours after injection from (mean +/- SD) 177 +/- 19 to 20,755 +/- 10,310-mu-g/24 hr (P < 0.01); the urinary IgG excretion increased from 5.8 +/- 2.9 to 236.1 +/- 132.2-mu-g/24 hr (P < 0.03); the selectivity index (clearance IgG/clearance albumin) decreased from 0.33 +/- 0.12 to 0.12 +/- 0.05 (P < 0.004).
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页码:115 / 123
页数:9
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