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High-glucose-induced structural changes in the heparan sulfate proteoglycan, perlecan, of cultured human aortic endothelial cells

机译:高葡萄糖诱导的人主动脉内皮细胞硫酸乙酰肝素蛋白聚糖,Perlecan的结构变化

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摘要

Hyperglycemia is an independent risk factor for diabetes-associated cardiovascular disease. One potential mechanism involves hyperglycemia-induced changes in arterial wall extracellular matrix components leading to increased atherosclerosis susceptibility. A decrease in heparan sulfate (HS) glycosaminoglycans (GAG) has been reported in diabetic arteries. The present studies examined the effects of high glucose on in vitro production of proteoglycans (PG) by aortic endothelial cells. Exposure of cells to high glucose (30 vs. 5 mM glucose) resulted in decreased [~(35)S] sodium sulfate incorporation specifically into secreted HSPG. Differences were not due to hyperosmolar effects and no changes were observed in CS/DSPG. Enzymatic procedures, immunoprecipitation and Western analyses demonstrated that high glucose induced changes specifically in the HSPG, perlecan. In double-label experiments, lower sulfate incorporation in high-glucose-treated cells was accompanied by lower [~3H] glucosamine incorporation into GAG but not lower [~3H] serine incorporation into PG core proteins. Size exclusion chromatography demonstrated that GAG size was unchanged and GAG sulfation was not reduced. These results indicate that the level of regulation of perlecan by high glucose is posttranslational, involving a modification in molecular structure, possibly a decrease in the number of HS GAG chains on the core protein.
机译:高血糖是糖尿病相关性心血管疾病的独立危险因素。一种潜在的机制涉及高血糖诱导的动脉壁细胞外基质成分的变化,导致动脉粥样硬化易感性增加。据报道,糖尿病动脉中硫酸乙酰肝素(HS)的糖胺聚糖(GAG)减少。本研究检查了高葡萄糖对主动脉内皮细胞蛋白聚糖(PG)体外生产的影响。细胞暴露于高葡萄糖(30 vs. 5 mM葡萄糖)会导致[〜(35)S]硫酸钠掺入分泌的HSPG中的浓度降低。差异不是由于高渗作用引起的,在CS / DSPG中未观察到变化。酶促程序,免疫沉淀法和Western分析表明,高糖诱导了HSPG(Perlecan)中的特异性变化。在双标记实验中,高糖处理细胞中硫酸盐的掺入量较低,而GAG中葡萄糖[[3H]]糖胺掺入量较低,而PG核心蛋白中丝氨酸[[3H]]掺入量较低。尺寸排阻色谱法表明GAG尺寸未改变,GAG硫酸化未降低。这些结果表明,高葡萄糖对珍珠白蛋白的调节水平是翻译后的,涉及分子结构的修饰,可能减少核心蛋白上HS GAG链的数量。

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