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MCP-1对LPS致炎小鼠子宫巨噬细胞迁移和功能活性的调节

丁慧芳 张玉玲 卢浩 张瑞平 钱志英 张顺利

中国免疫学杂志2017,Vol.33Issue(4):507-510,4.
中国免疫学杂志2017,Vol.33Issue(4):507-510,4.DOI:10.3969/j.issn.1000-484X.2017.04.006

MCP-1对LPS致炎小鼠子宫巨噬细胞迁移和功能活性的调节

Adjustment of MCP-1 to migration and functional activity on macrophages in uterine of inflammatory mice induced by LPS

丁慧芳 1张玉玲 1卢浩 1张瑞平 1钱志英 1张顺利1

作者信息

  • 1. 河南师范大学生命科学学院 省部共建细胞分化调控国家重点实验室,新乡453007
  • 折叠

摘要

Abstract

Objective:To explore the adjustment factors to the migration and functional activity on macrophages in the uterine of inflammatory mice induced by LPS.Methods:150 Kunming female mouse were divided into control group (group A),LPS model group (group B),MCP-1 blocking-up group (group C),the mice uterines were extracted separately at hour 1,3,6,12,24.The number of CD14+ macrophages and the expression of CD14 macrophages were detected by Immunohistochemistry,ELISA detects the expression of TNF-α and MCP-1.Results:①Compared with group A,the number of CD14+ macrophages and the expression of CD14 in endometrium,myometrium,perimrtrium of group B were highly significantly increased (P<0.01) at every time points,the endometrium,myometrium of group C were closely to normal level at 1,3,6 h;compared with group B,the number of CD14+ macrophages and the expression of CD14 were highly significantly decreased(P<0.01)at 1,3,6 h of perimrtrium of group C and every time points of endometrium,myometrium of group C.②Compared with group A,the content of TNF-α and MCP-1 were highly significantly increased (P<0.01) at every time points of group B and 12,24 h of group C;compared with group B,the content of TNF-α and MCP-1 of group C were highly significantly decreased(P<0.01) at every time points.Conclusion:The migration of macrophages and the expression of CD14 and TNF-α in the uterine of inflammatory mice induced by LPS were regulated by MCP-1.

关键词

MCP-1/LPS/巨噬细胞/CD14/TNF-α/子宫/小鼠

Key words

MCP-1/LPS/Macrophage/CD14/TNF-α/Uterus/Mice

分类

医药卫生

引用本文复制引用

丁慧芳,张玉玲,卢浩,张瑞平,钱志英,张顺利..MCP-1对LPS致炎小鼠子宫巨噬细胞迁移和功能活性的调节[J].中国免疫学杂志,2017,33(4):507-510,4.

基金项目

本文受河南省科技攻关项目(No.0524420040)和河南省动物学省级重点学科基金资助. (No.0524420040)

中国免疫学杂志

OA北大核心CSCDCSTPCD

1000-484X

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