Buono Chiara, Come Carolyn E, Stavrakis George, Maguire Graham F, Connelly Philip W, Lichtman Andrew H
Immunology Research Division, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, 221 Longwood Ave, Boston, MA 02115, USA.
Arterioscler Thromb Vasc Biol. 2003 Mar 1;23(3):454-60. doi: 10.1161/01.ATV.0000059419.11002.6E. Epub 2003 Jan 30.
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.
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.
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.
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。
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。
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。