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低密度脂蛋白(LDL)在体外可增强单核细胞与内皮细胞的黏附。

LDL enhances monocyte adhesion to endothelial cells in vitro.

作者信息

Alderson L M, Endemann G, Lindsey S, Pronczuk A, Hoover R L, Hayes K C

出版信息

Am J Pathol. 1986 May;123(2):334-42.

Abstract

Monocyte adhesion to the arterial endothelium is an early event in diet-induced atherogenesis. The possibility that low-density lipoprotein (LDL) may influence this adhesion was investigated by using an in vitro monolayer collection assay. Postprandial and fasting LDL was isolated from 12 normal adult human donors (8 male and 4 female) and incubated with primary cultures of bovine aortic endothelial cells (BAEC) for 6 hours. 51Cr-labeled mononuclear leukocytes (MNLs) were then added and incubated an additional 30 minutes. When results were expressed as the ratio of adherent counts per minute in LDL-treated BAEC cultures to that in PBS-treated controls, 10 of the 16 LDL samples isolated from male donors induced a significant increase (P less than 0.05) in MNL adhesion (1.06-1.27) attributable to esterase-positive cells. This increase was dose-dependent and maximal at 100 micrograms LDL protein/ml. The magnitude of the response was significantly correlated with LDL composition (r = 0.857, P less than 0.01) such that LDL rich in cholesterol and triglyceride relative to protein enhanced MNL adhesion, whereas lipid-poor LDL (typically isolated from the women) reduced adhesion.

摘要

单核细胞黏附于动脉内皮是饮食诱导动脉粥样硬化形成过程中的早期事件。通过体外单层收集试验研究了低密度脂蛋白(LDL)可能影响这种黏附的可能性。从12名正常成年人类供体(8名男性和4名女性)中分离出餐后和空腹LDL,并与牛主动脉内皮细胞(BAEC)原代培养物一起孵育6小时。然后加入51Cr标记的单核白细胞(MNLs),并再孵育30分钟。当结果表示为LDL处理的BAEC培养物中每分钟黏附计数与PBS处理的对照中每分钟黏附计数之比时,从男性供体分离的16个LDL样本中有10个诱导酯酶阳性细胞导致MNL黏附显著增加(P小于0.05)(1.06 - 1.27)。这种增加呈剂量依赖性,在100微克LDL蛋白/毫升时达到最大值。反应程度与LDL组成显著相关(r = 0.857,P小于0.01),即相对于蛋白质富含胆固醇和甘油三酯的LDL增强了MNL黏附,而脂质含量低的LDL(通常从女性中分离)降低了黏附。

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