Reduction of Heparan Sulphate-associated Anionic Sites in the Glomerular Basement Membrane of Rats with Streptozotocin-induced Diabetic Nephropathy
Overview
Authors
Affiliations
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.
Endothelial Toxicity of High Glucose and its by-Products in Diabetic Kidney Disease.
Dou L, Jourde-Chiche N Toxins (Basel). 2019; 11(10).
PMID: 31590361 PMC: 6833015. DOI: 10.3390/toxins11100578.
Endothelium structure and function in kidney health and disease.
Jourde-Chiche N, Fakhouri F, Dou L, Bellien J, Burtey S, Frimat M Nat Rev Nephrol. 2019; 15(2):87-108.
PMID: 30607032 DOI: 10.1038/s41581-018-0098-z.
Zimering M, Zhang J, Guarino P, Emanuele N, McCullough P, Fried L Front Endocrinol (Lausanne). 2014; 5:128.
PMID: 25157242 PMC: 4127944. DOI: 10.3389/fendo.2014.00128.
The endothelium in diabetic nephropathy.
Gilbert R Curr Atheroscler Rep. 2014; 16(5):410.
PMID: 24623181 DOI: 10.1007/s11883-014-0410-8.
Sugar T, Wassenhove-McCarthy D, Esko J, van Kuppevelt T, Holzman L, McCarthy K Kidney Int. 2013; 85(2):307-18.
PMID: 23924956 PMC: 4624314. DOI: 10.1038/ki.2013.281.