首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Glycosaminoglycan Regulation by VEGFA and VEGFC of the Glomerular Microvascular Endothelial Cell Glycocalyx in Vitro
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Glycosaminoglycan Regulation by VEGFA and VEGFC of the Glomerular Microvascular Endothelial Cell Glycocalyx in Vitro

机译:VEGFA和VEGFC对体外肾小球微血管内皮细胞糖萼的糖胺聚糖调节作用

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摘要

Damage to endothelial glycocalyx impairs vascular barrier function and may contribute to progression of chronic vascular disease. An early indicator is microalbuminuria resulting from glomerular filtration barrier damage. We investigated the contributions of hyaluronic acid (HA) and chondroitin sulfate (CS) to glomerular microvascular endothelial cell (GEnC) glycocalyx and examined whether these are modified by vascular endothelial growth factors A and C (VEGFA and VEGFC). HA and CS were imaged on GEnCs and their resynthesis was examined. The effect of HA and CS on transendothelial electrical resistance (TEER) and labeled albumin flux across monolayers was assessed. Effects of VEGFA and VEGFC on production and charge characteristics of glycosaminoglycan (GAG) were examined via metabolic labeling and liquid chromatography. GAG shedding was quantified using Alcian Blue. NDST2 expression was examined using real-time PCR. GEnCs expressed HA and CS in the glycocalyx. CS contributed to the barrier to both ion (TEER) and protein flux across the monolayer; HA had only a limited effect. VEGFC promoted HA synthesis and increased the charge density of synthesized GAGs. In contrast, VEGFA induced shedding of charged GAGs. CS plays a role in restriction of macromolecular flux across GEnC monolayers, and VEGFA and VEGFC differentially regulate synthesis, charge, and shedding of GAGs in GEnCs. These observations have important implications for endothelial barrier regulation in glomerular and other microvascular beds.
机译:对内皮糖萼的损害会损害血管屏障功能,并可能导致慢性血管疾病的进展。早期指标是由肾小球滤过屏障损害引起的微量白蛋白尿。我们调查了透明质酸(HA)和硫酸软骨素(CS)对肾小球微血管内皮细胞(GEnC)糖萼的贡献,并检查了它们是否被血管内皮生长因子A和C(VEGFA和VEGFC)修饰。 HA和CS在GEnC上成像并检查了它们的再合成。评估了HA和CS对跨内皮电阻(TEER)和跨单层标记白蛋白通量的影响。通过代谢标记和液相色谱检查了VEGFA和VEGFC对糖胺聚糖(GAG)的产生和电荷特性的影响。使用阿尔辛蓝定量GAG脱落。使用实时PCR检查NDST2表达。 GEnC在糖萼中表达HA和CS。 CS阻碍了离子(TEER)和蛋白质通过单层的通量。 HA的作用有限。 VEGFC促进HA合成并增加合成GAG的电荷密度。相反,VEGFA诱导带电的GAG脱落。 CS在限制跨GEnC单层的大分子通量中发挥作用,而VEGFA和VEGFC差异性调节GEnC中GAG的合成,电荷和脱落。这些观察对于肾小球和其他微血管床的内皮屏障调节具有重要意义。

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