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干扰素-γ对低密度脂蛋白受体缺陷小鼠饮食诱导动脉粥样硬化的程度及表型的影响

Influence of interferon-gamma on the extent and phenotype of diet-induced atherosclerosis in the LDLR-deficient mouse.

作者信息

Buono Chiara, Come Carolyn E, Stavrakis George, Maguire Graham F, Connelly Philip W, Lichtman Andrew H

机构信息

Immunology Research Division, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2003 Mar 1;23(3):454-60. doi: 10.1161/01.ATV.0000059419.11002.6E. Epub 2003 Jan 30.

Abstract

OBJECTIVE

The aim of this study was to investigate the influence of interferon-gamma (IFN-gamma) on atherosclerosis in low density lipoprotein receptor (LDLR)-null mice.

METHODS AND RESULTS

We cross-bred IFN-gamma-deficient mice with LDLR-null mice and analyzed lipoprotein profiles and atherosclerosis in the compound mutant progeny after 8 and 20 weeks on a cholesterol-enriched diet. IFN-gamma deficiency did not affect serum cholesterol levels or lipoprotein profiles, but it did affect the extent and phenotype of atherosclerosis. Atherosclerotic lesions in IFN-gamma-deficient mice were reduced by 75% in the aortic arch and by 46% in the descending aorta compared with control mice after 8 weeks on the diet. After 20 weeks, arch lesions were reduced by 43%, and descending aorta lesions were reduced by 65% in IFN-gamma-deficient mice compared with controls. At 8 weeks, percent lesional macrophage and smooth muscle content was significantly less in the IFN-gamma-deficient mice, but not at 20 weeks. Although there were fewer class II major histocompatibility complex-positive cells in the lesions of IFN-gamma-deficient animals compared with controls, class II major histocompatibility complex expression on endothelial cells overlying lesions persisted in the absence of IFN-gamma.

CONCLUSIONS

These data provide direct evidence that IFN-gamma influences atherosclerosis development and phenotype in the LDLR-deficient mouse, independent of changes in blood lipoprotein profiles.

摘要

目的

本研究旨在探讨干扰素-γ(IFN-γ)对低密度脂蛋白受体(LDLR)基因敲除小鼠动脉粥样硬化的影响。

方法与结果

我们将IFN-γ基因缺陷小鼠与LDLR基因敲除小鼠进行杂交,并在富含胆固醇的饮食喂养8周和20周后,分析复合突变后代的脂蛋白谱和动脉粥样硬化情况。IFN-γ缺乏不影响血清胆固醇水平或脂蛋白谱,但确实影响动脉粥样硬化的程度和表型。与对照小鼠相比,饮食喂养8周后,IFN-γ基因缺陷小鼠主动脉弓处的动脉粥样硬化病变减少了75%,降主动脉处减少了46%。20周后,与对照相比,IFN-γ基因缺陷小鼠主动脉弓病变减少了43%,降主动脉病变减少了65%。在8周时,IFN-γ基因缺陷小鼠病变处的巨噬细胞和平滑肌含量百分比显著降低,但在20周时未出现这种情况。尽管与对照相比,IFN-γ基因缺陷动物病变处的II类主要组织相容性复合体阳性细胞较少,但在缺乏IFN-γ的情况下,病变上方内皮细胞上的II类主要组织相容性复合体表达仍持续存在。

结论

这些数据提供了直接证据,表明IFN-γ影响LDLR缺陷小鼠的动脉粥样硬化发展和表型,且与血液脂蛋白谱的变化无关。

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