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高血糖、胰岛素和肝素对血管内皮蛋白聚糖和乙酰肝素酶基因表达的改变。

Alteration of endothelial proteoglycan and heparanase gene expression by high glucose, insulin and heparin.

机构信息

Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, S7N 5B4, Canada.

出版信息

Vascul Pharmacol. 2013 Sep-Oct;59(3-4):112-8. doi: 10.1016/j.vph.2013.08.001. Epub 2013 Aug 11.

Abstract

Heparan sulfate proteoglycans (HSPGs) contain a core protein with glycosaminoglycans attached. Reduced glycosaminoglycan, in endothelial HSPGs syndecan and perlecan, is associated with diabetic cardiovascular complications but changes in core protein remain controversial. Since heparanase degrades heparan sulfate, we wished to determine if changes in endothelial heparanase mRNA, by high glucose (HG), correlate with changes in syndecan and perlecan core proteins, and to observe effects of heparin or insulin. RNA was isolated from cultured human aortic endothelial cells treated with HG (30mM), insulin (0.01 units/mL), heparin (0.5μg/mL), HG plus heparin and/or insulin for 24h. Real time PCR revealed that HG alone significantly increased heparanase, decreased syndecan with no effect on perlecan mRNA. Heparin or insulin significantly prevented the increase in heparanase but decreased perlecan mRNA while heparin, but not insulin, prevented the decrease in syndecan mRNA in HG treated cells. HG plus heparin and insulin increased heparanase and syndecan mRNA compared to all other treatments and decreased perlecan mRNA compared to control and HG alone. Heparin may protect endothelium from HG injury by reducing heparanase and increasing syndecan while insulin inhibits heparanase expression. Effects with insulin plus heparin suggest interference in transcriptional regulation of heparanase and syndecan genes.

摘要

硫酸乙酰肝素蛋白聚糖 (HSPGs) 含有与糖胺聚糖相连的核心蛋白。内皮细胞 HSPGs 连接蛋白聚糖和多配体聚糖的糖胺聚糖减少与糖尿病心血管并发症有关,但核心蛋白的变化仍存在争议。由于硫酸乙酰肝素酶可降解硫酸乙酰肝素,我们希望确定高葡萄糖 (HG) 对内皮细胞硫酸乙酰肝素酶 mRNA 的影响是否与连接蛋白聚糖和多配体聚糖核心蛋白的变化相关,并观察肝素或胰岛素的作用。将培养的人主动脉内皮细胞用 HG(30mM)、胰岛素(0.01 单位/mL)、肝素(0.5μg/mL)、HG 加肝素和/或胰岛素处理 24 小时后分离 RNA。实时 PCR 显示,HG 单独处理可显著增加肝素酶,降低连接蛋白聚糖,但对多配体聚糖 mRNA 无影响。肝素或胰岛素可显著阻止肝素酶的增加,但降低 HG 处理细胞中的多配体聚糖 mRNA,而肝素但不是胰岛素可防止 HG 处理细胞中连接蛋白聚糖 mRNA 的减少。HG 加肝素和胰岛素增加了肝素酶和连接蛋白聚糖 mRNA,与其他所有处理相比,多配体聚糖 mRNA 减少,与对照和 HG 单独处理相比。肝素可能通过降低肝素酶和增加连接蛋白聚糖来保护内皮细胞免受 HG 损伤,而胰岛素抑制肝素酶的表达。胰岛素加肝素的作用表明,肝素酶和连接蛋白聚糖基因的转录调控受到干扰。

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