Abstract

BackgroundHeparan sulfate proteoglycans (HSPGs) contain glycosaminoglycan (GAG) chains made primarily of heparan sulfate (HS). Hyperglycemia in diabetes leads to endothelial injury and nephropathy, retinopathy and atherosclerosis. Decreased HSPG may contribute to diabetic endothelial injury. Decreased tissue HS in diabetes has been reported, however, endothelial HS changes are poorly studied.ObjectiveTo determine total GAGs, including HS, in endothelium under hyperglycemic conditions and the protective effect of insulin and heparin.MethodsConfluent primary porcine aortic endothelial cells (PAECs) were divided into control, glucose (30 mM), insulin (0.01 unit/ml) and glucose plus insulin treatment groups for 24, 48 and 72 hours. Additionally, PAECs were treated with glucose, heparin (0.5 μg/ml) and glucose plus heparin for 72 hours. GAGs were isolated from cells and medium. GAG concentrations were determined by the carbazole assay and agarose gel electrophoresis.ResultsGAGs were significantly increased only in control and glucose plus insulin groups at 72 versus 24 hours. Glucose decreased cell GAGs and increased medium GAGs, and insulin alone decreased cell GAGs at all times compared to control. In the glucose plus insulin group, cell GAGs were less than control at 24 hours, and greater than glucose or insulin alone at 48 and 72 hours while GAGs in medium were greater than control at all times and glucose at 72 hours. Heparin increased GAGs in glucose treated cells and medium.ConclusionHigh glucose and insulin alone reduces endothelial GAGs. In hyperglycemic conditions, heparin or insulin preserves GAGs which may protect cells from injury. Insulin is an effective diabetic therapy since it not only lowers blood glucose, but also protects endothelium.

Highlights

  • Heparan sulfate proteoglycans (HSPGs) contain glycosaminoglycan (GAG) chains made primarily of heparan sulfate (HS)

  • In the glucose plus insulin group, cell GAGs were less than control at 24 hours, and greater than glucose or insulin alone at 48 and 72 hours while GAGs in medium were greater than control at all times and glucose at 72 hours

  • endothelial cell (EC) are targets for hyperglycemia in diabetes mellitus resulting in cardiovascular complications

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Summary

Introduction

Heparan sulfate proteoglycans (HSPGs) contain glycosaminoglycan (GAG) chains made primarily of heparan sulfate (HS). Decreased HSPG may contribute to diabetic endothelial injury. HS is a prominent blood vessel component and the most common GAG found on the endothelial cell (EC) surface and in the ECM. The interaction of HS side chains with bioactive factors controls physiological processes of embryonic development, tissue repair, blood coagulation, cartilage function and glomerular filtration [1,3,4]; and pathological processes of wound healing, vessel formation, and tumor cell growth, adhesion, invasiveness and metastasis [5]. As well as structural and functional alterations of their GAG components, are associated with cardiovascular disease, cancer, inflammation, amyloidosis and diabetes [6,7,8,9]

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