巨细胞病毒感染小鼠主动脉早期动脉粥样硬化斑块。

K Berencsi, V Endresz, D Klurfeld, L Kari, D Kritchevsky, E Gönczöl
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引用次数: 63

摘要

我们在这里发现,接种了小鼠巨细胞病毒(MCMV)的BALB/c小鼠在主动脉壁的内皮细胞和平滑肌细胞中表达病毒抗原,并且在主动脉腔中炎症细胞的积累,类似于在人类早期动脉粥样硬化病变中看到的,与病毒抗原表达位点共定位。病毒感染时对小鼠的免疫抑制增加了病毒抗原的表达和内膜早期动脉粥样硬化病变的大小。低密度脂蛋白胆固醇(LDL-C)是动脉粥样硬化斑块的主要脂质贡献者,在mcmv感染小鼠的血清中,无论小鼠是否被喂食高胆固醇饮食,其百分比都显着增加。人巨细胞病毒(HCMV)显著增加体外感染人动脉平滑肌细胞系总胆固醇的酯化胆固醇成分。这些结果表明CMV感染参与了导致动脉粥样硬化发展的两个主要机制,即免疫损伤和高LDL-C。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early atherosclerotic plaques in the aorta following cytomegalovirus infection of mice.

We show here that BALB/c mice inoculated with murine cytomegalovirus (MCMV) express viral antigens in the endothelial and smooth muscle cells of the aortic wall, and that accumulation of inflammatory cells in the aortic lumen, similar to that seen in early atherosclerotic lesions in humans, colocalizes with the site of virus antigen expression. Immunosuppression of the mice at the time of virus infection increased the expression of viral antigens and the size of early atherosclerotic lesions in the intima. The percentage of the low-density lipoprotein cholesterol (LDL-C), the major lipid contributor to atherosclerotic plaques, was significantly increased in the serum of MCMV-infected mice, whether or not the mice were fed a high cholesterol diet. Human cytomegalovirus (HCMV) significantly increased the esterified cholesterol component of the total cholesterol in a human arterial smooth muscle cell line infected in vitro with HCMV. These results suggest that CMV infection is involved in two of the major mechanisms that lead to development of atherosclerosis, i.e., immune injury and high LDL-C.

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