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载脂蛋白AI对单核细胞表型与MCP⁃1/CCR2的影响

尹建国 张社兵 彭道泉

中国医科大学学报2017,Vol.46Issue(6):501-504,4.
中国医科大学学报2017,Vol.46Issue(6):501-504,4.DOI:10.12007/j.issn.0258⁃4646.2017.06.005

载脂蛋白AI对单核细胞表型与MCP⁃1/CCR2的影响

Effect of Apolipoprotein AI on MCP?1 Plasma Levels,Monocyte Subset Proportions,and in Vitro CCR2 Expression

尹建国 1张社兵 2彭道泉1

作者信息

  • 1. 汕头大学医学院附属粤北人民医院心血管内科,广东 韶关 512026
  • 2. 中南大学湘雅二医院心血管内科,长沙 410011
  • 折叠

摘要

Abstract

Objective To explore effects of apoAI on MCP?1 levels in the plasma and the Ly6Chi monocyte proportion in the blood and spleen of atherosclerotic mice,as well as on CCR2 expression in vitro. Methods Sixteen male apoE?/?mice were fed with high cholesterol diet for 12 weeks. Mice were randomly divided into control and apoAI groups and were administered with PBS or apoAI(40 mg/kg),respectively,via tail vein on the 1st and 3rd day before sacrifice. Mice in both groups were administered LPS(25μg/mouse)via intraperitoneal injection 12 h before sacrifice. Plas?ma levels of MCP?1 were determined using ELISA,and the Ly6Chi monocyte proportion was analyzed using flow cytometry. In addition,human monocytic THP?1 cells were randomly divided into control and apoAI(10 mg/L)?treated groups,pretreated with corresponding intervention,and incubated with LPS(10μg/L). CCR2 expression levels were measured by Western blotting. Results Compared with the control treatment, apoAI treatment remarkably reduced MCP?1 levels in plasma and Ly6Chi monocyte proportion in the blood and spleen(P<0.01). Furthermore, apoAI treatment inhibited CCR2 expression in monocytes in vitro(P<0.05). Conclusion apoAI can reduce MCP?1 levels in plasma and the Ly6Chi monocyte proportion in the blood and spleen and can inhibit CCR2 expression in monocytes in vitro.

关键词

载脂蛋白AI/单核细胞表型/单核细胞趋化蛋白1/CC类趋化因子受体2

Key words

apolipoprotein AI/monocyte subset/monocyte chemotactic protein 1/CC⁃chemokine receptor 2

分类

医药卫生

引用本文复制引用

尹建国,张社兵,彭道泉..载脂蛋白AI对单核细胞表型与MCP⁃1/CCR2的影响[J].中国医科大学学报,2017,46(6):501-504,4.

基金项目

国家自然科学基金(81370393) (81370393)

中国医科大学学报

OA北大核心CSCDCSTPCD

0258-4646

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