中文摘要：

目的：研究高脂饲料饲养ApoE-/-小鼠建立动脉粥样硬化动物模型的过程中CD11b＋Gr-1＋髓系抑制性细胞的变化趋势,以期揭示高脂血症导致动脉粥样硬化的另一种可能的细胞机制。方法：将12只雄性ApoE-/-小鼠随机分为对照组（n=6）和模型组（n=6）,分别给予普通饲料与高脂饲料处理。8周后酶法和免疫比浊法检测血清甘油三酯（TG）、总胆固醇（TC）、低密度脂蛋白胆固醇（LDL-C）、高密度脂蛋白胆固醇（HDL-C）、载脂蛋白A-I（apoA-I）和载脂蛋白B（apoB）水平;HE染色观察主动脉病理形态学改变;油红O染色观察内皮下间隙脂质沉积情况;流式细胞术分析骨髓、脾脏、外周血中CD11b＋Gr-1＋髓系抑制性细胞的百分比,比较其与对照组之间的差异度。结果：8周的高脂饲喂使得ApoE-/-小鼠血脂水平显著改变,动脉粥样硬化斑块明显形成,CD11b＋Gr-1＋髓系抑制性细胞占骨髓单个核细胞比例显著升高,并进一步被动员释放到外周组织,导致循环中CD11b＋Gr-1＋髓系抑制性细胞显著增加。结论：高脂饲料饲养ApoE-/-小鼠能使CD11b＋Gr-1＋髓系抑制性细胞的生成显著增加,并向循环和外周组织释放。高脂血症可能是通过激活CD11b＋Gr-1＋髓系抑制性细胞的途径来参与动脉粥样硬化的发生、发展。

英文摘要：

Objective： To study the variation trend of CD11b＋Gr-1＋myeloid derived suppressor cells（MDSCs） in ApoE-/-mice during the formation of their atherosclerosis by high-fat diet,and furthermore to explore the cellular mechanism of hyperlipidemia-induced atherosclerosis.Methods：Total 12 male ApoE-/-mice were randomly divided into control group（n=6）and model group（n=6）,respectively fed with normal diet and high-fat diet.After 8 weeks,serum lipid levels（total triglyeride,total cholesterol,HDL cholesterol,LDL cholesterol,apoA-I and apoB） were measured by enzymatic method and by immunoturbidimetery.Lesions of aortic arteries were stained with hematoxylin eosin.Lipid-accumulation in subendothelial space was observed by oil red O staining.The percent of bone marrow,spleen,and peripheral blood CD11b＋Gr-1＋MDSCs was measured by flow cytometry analysis,and compared with the control group.Results：High-fat diet for 8 weeks made a significant change of serum lipid and made ApoE-/-mice form obviously atherosclerotic plaque.The percent of CD11b ＋Gr-1＋MDSCs in total mononuclear cells of bone marrow was significantly increased,and furthermore,these cells were mobilized and released into the peripheral tissue;consequently,the amount of CD11b＋Gr-1＋MDSCs in spleen and circulating pool increased significantly.Conclusion：Bone marrow CD11b＋Gr-1＋MDSCs of ApoE-/-mice fed with high-fat diet can be mobilized and be released to the circulation and peripheral tissue.It indicates that hyperlipidemia may participate in the formation and development of atherosclerosis by activating CD11b＋Gr-1＋MDSCs pathway.