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双酚 A 对小鼠腹腔巨噬细胞极化影响的体外研究

李美玲 李应配 冷银芝 蒋建华 朱启星 沈彤

安徽医科大学学报Issue(6):782-786,5.
安徽医科大学学报Issue(6):782-786,5.

双酚 A 对小鼠腹腔巨噬细胞极化影响的体外研究

Effects of bisphenol A on polarization of mice peritoneal macrophage in vitro

李美玲 1李应配 1冷银芝 1蒋建华 2朱启星 3沈彤1

作者信息

  • 1. 安徽医科大学公共卫生学院卫生毒理学系,合肥 230032
  • 2. 安徽医科大学第一附属医院临床营养科,合肥 230022
  • 3. 安徽医科大学公共卫生学院职业卫生与环境卫生学系,合肥 230032
  • 折叠

摘要

Abstract

Objective To explore the effect of bisphenol A(BPA)on the polarization of mice peritoneal macro-phage in vitro. Methods Peritoneal macrophages isolated from C57BL/ 6J male mice were stimulated with murine (10 ng / ml)IFN-γ and LPS(500 ng / ml)for induction of M1-type macrophages,and(10 ng / ml)IL-4 for M2-type,respectively. Meanwhile cells were treated with 0. 1,1 and 10 μmol/ L BPA,blank control group and vehicle control group were established at the same time. The proportions of M1-type and M2-type macrophages were deter-mined by FACS analysis,the activities of iNOS(cytokines secreted by M1)and Arg-1(cytokines secreted by M2) were measured by ELISA assay. Results Different concentrations of BPA promoted M1-type polarization of mice peritoneal macrophage induced by IFN-γ and LPS. Compared with the blank control group,M1 type proportion was increased by 11. 3% and 17. 4% ,and iNOS activity was elevated by 1. 95 and 2. 29 times in 1 and 10 μmol/ L BPA group respectively,and the differences were statistically significant. Different concentrations of BPA inhibited M2-type polarization of mice peritoneal macrophage induced by IL-4. Compared with the blank control group,M2 type proportion was decreased by 9% and 14. 3% and Arg-1 activity was reduced by 0. 37 and 0. 49 times in 1 and 10 μmol/ L BPA group respectively,and the differences were statistically significant. Conclusion Low dose expo-sure of BPA can promote M1-type polarization of mice peritoneal macrophage,while inhibit M2-type polarization in vitro.

关键词

双酚 A/巨噬细胞/极化

Key words

bisphenol A/macrophages/polarization

分类

医药卫生

引用本文复制引用

李美玲,李应配,冷银芝,蒋建华,朱启星,沈彤..双酚 A 对小鼠腹腔巨噬细胞极化影响的体外研究[J].安徽医科大学学报,2015,(6):782-786,5.

基金项目

国家自然科学基金 ()

安徽医科大学学报

OA北大核心CSTPCD

1000-1492

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