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内皮细胞对氧化脂蛋白的反应决定了小鼠动脉粥样硬化的遗传易感性。

Endothelial responses to oxidized lipoproteins determine genetic susceptibility to atherosclerosis in mice.

作者信息

Shi W, Haberland M E, Jien M L, Shih D M, Lusis A J

机构信息

Department of Medicine, University of California Los Angeles 90095- 1679, USA.

出版信息

Circulation. 2000 Jul 4;102(1):75-81. doi: 10.1161/01.cir.102.1.75.

Abstract

BACKGROUND

Oxidized LDL has been found within the subendothelial space, and it exhibits numerous atherogenic properties, including induction of inflammatory genes. We examined the possibility that variations in endothelial response to minimally modified LDL (MM-LDL) constitute one of the genetic components in atherosclerosis.

METHODS AND RESULTS

By a novel explant technique, endothelial cells (ECs) were isolated from the aorta of inbred mouse strains with different susceptibilities to diet-induced atherosclerosis. Responses to MM-LDL were evaluated by examining the expression of inflammatory genes involved in atherosclerosis, including monocyte chemotactic protein-1 (MCP-1) and macrophage-colony-stimulating factor (M-CSF), an oxidative stress gene, heme oxygenase-1 (HO-1), and other, noninflammatory, genes. ECs from the susceptible mouse strain C57BL/6J exhibited dramatic induction of MCP-1, M-CSF, and HO-1, whereas ECs from the resistant strain C3H/HeJ showed little or no induction. In contrast, ECs from the 2 strains responded similarly to lipopolysaccharide.

CONCLUSIONS

These data provide strong evidence that genetic factors in atherosclerosis act at the level of the vessel wall.

摘要

背景

氧化型低密度脂蛋白已在血管内皮间隙中被发现,并且具有众多致动脉粥样硬化特性,包括诱导炎症基因。我们研究了内皮细胞对轻度修饰的低密度脂蛋白(MM-LDL)反应的差异构成动脉粥样硬化遗传因素之一的可能性。

方法与结果

通过一种新的外植技术,从对饮食诱导的动脉粥样硬化易感性不同的近交系小鼠品系的主动脉中分离出内皮细胞(ECs)。通过检测参与动脉粥样硬化的炎症基因的表达来评估对MM-LDL的反应,这些基因包括单核细胞趋化蛋白-1(MCP-1)和巨噬细胞集落刺激因子(M-CSF)、一个氧化应激基因血红素加氧酶-1(HO-1)以及其他非炎症基因。来自易感小鼠品系C57BL/6J的内皮细胞表现出MCP-1、M-CSF和HO-1的显著诱导,而来自抗性品系C3H/HeJ的内皮细胞则几乎没有或没有诱导。相比之下,这两个品系的内皮细胞对脂多糖的反应相似。

结论

这些数据提供了有力证据,表明动脉粥样硬化中的遗传因素在血管壁水平起作用。

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