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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Degradation of the endothelial glycocalyx is associated with chylomicron leakage in mouse cremaster muscle microcirculation.
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Degradation of the endothelial glycocalyx is associated with chylomicron leakage in mouse cremaster muscle microcirculation.

机译:内皮糖萼的降解与小鼠提睾肌微循环中乳糜微粒的泄漏有关。

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摘要

A thick endothelial glycocalyx contributes to the barrier function of vascular endothelium in macro- and microcirculation. We hypothesised in the current study that diet-induced hyperlipidaemia perturbs the glycocalyx, resulting in decreased dimensions of this layer and increased transendothelial lipoprotein leakage in capillaries. Glycocalyx thickness was measured in mouse cremaster muscle capillaries by intravital microscopy from the distance between flowing red blood cells and the endothelial surface. In control C57BL/6 mice on standard chow, glycocalyx thickness measured 0.58 +/- 0.01 (mean +/- SEM) mum, and no lipoproteins were observed in the tissue. After three months administration of an either mild or severe high-fat / high-cholesterol diet (HFC) to C57BL/6 and ApoE3-Leiden mice, circulating large lipoproteins appeared into the subendothelial space in an increasing proportion of cremaster capillaries, and these capillaries displayed reduced glycocalyx dimensions of 0.40 +/- 0.02 and 0.30 +/- 0.01 mum (C57BL/6 mice), and 0.37 +/- 0.01 and 0.28 +/- 0.01 mum (ApoE3-Leiden mice), after the mild and severe HFC diet, respectively. The chylomicron nature of the accumulated lipoproteins was confirmed by observations of subendothelial deposition of DiI-labeled chylomicrons in capillaries after inducing acute glycocalyx degradation by heparitinase in normolipidaemic C57BL/6 mice. It is concluded that while under control conditions the endothelial glycocalyx contributes to the vascular barrier against transvascular lipoprotein leakage in the microcirculation, diet-induced hyperlipidaemia reduces the thickness of the glycocalyx, thereby facilitating leakage of chylomicrons across the capillary wall.
机译:厚的内皮糖萼有助于大和微循环中血管内皮的屏障功能。在当前的研究中,我们假设饮食引起的高脂血症会扰乱糖萼,导致该层的尺寸减小,并增加毛细血管中跨内皮脂蛋白的泄漏。通过活体显微镜检查从流动的红细胞和内皮表面之间的距离,在小鼠睾丸肌毛细血管中测定糖萼厚度。在标准食物的对照C57BL / 6小鼠中,糖萼厚度测得为0.58 +/- 0.01(平均+/- SEM),并且在组织中未观察到脂蛋白。在对C57BL / 6和ApoE3-Leiden小鼠轻度或重度高脂/高胆固醇饮食(HFC)给药三个月后,循环中的大脂蛋白以越来越多的cremaster毛细血管和这些毛细血管出现在内皮下间隙在轻度和重度HFC之后,显示出的糖萼尺寸减少了0.40 +/- 0.02和0.30 +/- 0.01毫米(C57BL / 6小鼠)以及0.37 +/- 0.01和0.28 +/- 0.01毫米(ApoE3-Leiden小鼠)饮食分别。在正常血脂血症的C57BL / 6小鼠中,肝素酶诱导急性糖萼降解后,通过观察DiI标记的乳糜微粒在毛细血管中的内皮下沉积,证实了积累的脂蛋白的乳糜微粒性质。结论是,尽管在控制条件下内皮糖萼有助于微循环中抗跨血管脂蛋白渗漏的血管屏障,但饮食诱导的高脂血症会降低糖萼的厚度,从而促进乳糜微粒通过毛细血管壁渗漏。

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