Regulation of Glomerular Endothelial Cell Proteoglycans by Glucose.
10.3346/jkms.2004.19.2.245
- Author:
Tae Sun HA
1
;
Senthil DURAISAMY
;
Jennifer L FAULKNER
;
Balakuntalam S KASINATH
Author Information
1. Department of Pediatrics, Chungbuk National University, Cheongju, Korea. tsha@med.chungbuk.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S.
- Keywords:
Diabetes Mellitus;
Diabetic Nephropathies;
Endothelium;
Heparan Sulfate Proteoglycan;
Kidney Glomerulus;
Proteinuria
- MeSH:
Animals;
Basement Membrane/drug effects/metabolism;
Cattle;
Cells, Cultured;
Diabetic Nephropathies/metabolism;
Endothelial Cells/cytology/*drug effects/*metabolism;
Gene Expression/drug effects;
Glucose/*pharmacology;
Heparan Sulfate Proteoglycan/genetics/*metabolism;
Kidney Glomerulus/*cytology;
Sulfur Radioisotopes/diagnostic use;
Support, Non-U.S. Gov't;
Support, U.S. Gov't, Non-P.H.S.;
Support, U.S. Gov't, P.H.S.
- From:Journal of Korean Medical Science
2004;19(2):245-252
- CountryRepublic of Korea
- Language:English
-
Abstract:
The presence of heparan sulfate proteoglycan (HSPG) in anionic sites in the lamina rara interna of glomerular basement membrane suggests that the proteoglycan may be deposited by the glomerular endothelial cells (GEndo). We have previously demonstrated that bovine GEndo in vitro synthesize perlecan, a species of glomerular basement membrane HSPG. In this study we examined whether high glucose medium regulates the GEndo metabolism of glycopeptides including perlecan. Metabolic labeling of glycoconjugates with 35S-SO4, sequential ion exchange and Sepharose CL-4B chromatography of labeled glycoconjugates, and northern analysis were performed. Incubation of GEndo for 8 to 14 weeks (but not for 1-2 weeks) in medium containing 30 mM glucose resulted in nearly 50% reduction in the synthesis of cell layer and medium 35SO4-labeled low anionic glycoproteins and proteoglycans, including that of basement membrane HSPG (Kav 0.42) compared to GEndo grown in 5 mM glucose medium; no changes in anionic charge density or hydrodynamic size of proteoglycans were noted. Northern analysis demonstrated that the mRNA abundance of perlecan was reduced by 47% in cells incubated with 30 mM glucose. Our data suggest that high glucose medium reduces the GEndo synthesis of perlecan by regulating its gene expression. Reduced synthesis of perlecan by GEndo may contribute to proteinuria seen in diabetic nephropathy.
