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氧化型低密度脂蛋白诱导人内皮细胞高黏附性的调节剂

Modulators of oxidized LDL-induced hyperadhesiveness in human endothelial cells.

作者信息

Maier J A, Barenghi L, Bradamante S, Pagani F

机构信息

Dipartimento di Scienze e Tecnologie Biomediche-Ospedale San Raffaele, Milano, Italy.

出版信息

Biochem Biophys Res Commun. 1994 Oct 28;204(2):673-7. doi: 10.1006/bbrc.1994.2512.

Abstract

The adherence of monocytes to the endothelium is an early event in atherogenesis. Our previous studies have demonstrated that oxidized LDL induced U937 cells-endothelial interactions and that HDL prevented oxidized LDL effects. Here, we provide evidence that treatment of endothelial cells with the anti-inflammatory agent indomethacin abolished oxidized LDL as well as interleukin 1- and lipopolysaccharide-stimulated U937 adhesion. It is noteworthy that HDL, which is known to be protective against atherosclerosis, was effective only in negating U937 adhesion induced by oxidized LDL, while it did not affect interleukin 1- and lipopolysaccharide-induced hyperadhesiveness in endothelial cells. Since indomethacin inhibits cyclooxygenase which is the key enzyme in the synthesis of prostanoids, we have studied the effect of oxidized LDL on the expression of cyclooxygenase type 2 and demonstrated that oxidized LDL induces a sustained increase in the expression of cyclooxygenase mRNA.

摘要

单核细胞与内皮细胞的黏附是动脉粥样硬化形成过程中的早期事件。我们之前的研究表明,氧化型低密度脂蛋白(ox-LDL)可诱导U937细胞与内皮细胞相互作用,而高密度脂蛋白(HDL)可阻止氧化型低密度脂蛋白的作用。在此,我们提供证据表明,用抗炎药物吲哚美辛处理内皮细胞可消除氧化型低密度脂蛋白以及白细胞介素1和脂多糖刺激的U937细胞黏附。值得注意的是,已知对动脉粥样硬化具有保护作用的HDL仅能有效抵消氧化型低密度脂蛋白诱导的U937细胞黏附,而不影响白细胞介素1和脂多糖诱导的内皮细胞高黏附性。由于吲哚美辛可抑制环氧化酶(它是前列腺素合成中的关键酶),我们研究了氧化型低密度脂蛋白对环氧化酶2型表达的影响,并证明氧化型低密度脂蛋白可诱导环氧化酶mRNA表达持续增加。

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