| 注册
首页|期刊导航|中国畜牧兽医|羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立

羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立

孙春辉 郎需龙 杨艳玲 王秀然 李晓燕 卜昭阳 王兴龙

中国畜牧兽医2011,Vol.38Issue(3):199-203,5.
中国畜牧兽医2011,Vol.38Issue(3):199-203,5.

羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立

Eestablishment of Model that Virulent Brucella melitensi strain 16M Infect Mouse Macrophages

孙春辉 1郎需龙 2杨艳玲 3王秀然 1李晓燕 2卜昭阳 1王兴龙2

作者信息

  • 1. 吉林大学畜牧兽医学院,吉林,长春,130062
  • 2. 中国人民解放军军事医学科学院军事兽医研究所,吉林,长春,130122
  • 3. 中国人民解放军军事医学科学院军事兽医研究所,吉林,长春,130122,
  • 折叠

摘要

Abstract

Macrophage was the strongest anti-body cells of phagocytosis, while, Brucella could multiply in the cell and could not be killed. Therefor,we established the infection model,for continuous research Brucella and it's the host cell,and the interaction of baceria cell and host cell surface-associated membrane protein,discovering the intracellular interaction mechanism for next step. Infection of mouse macrophage cell line RAW264.7 with Brucella melitensi virulent strain 16M were performed 4 h at a cell/bacteria ratio of 1 : 500. Brucella-infected marophages were examined by indirect immunofluorescence assay and transmission electron microscopy assay. The optimal concentration ratio of primary antibody and secondary antibody in indirect immunofluorescence assay were 1 : 80 and 1 : 80, and the membrane depression and the endocytosis bodies were observed by transmission electron microscope. Expriment reduced the environmental factors of the infection process, optimized concentration ratio of primary and secondary antibodies in indirect immunofluorescence assay,established infection model.

关键词

羊布鲁氏菌强毒株16M/巨噬细胞系RAW264.7/间接免疫荧光试验/透射电镜试验

Key words

virulent Brucella melitensi strain 16M/macrophage cell line RAW264.7/indirect immunofluorescence assay/ electron microscope assay

分类

农业科技

引用本文复制引用

孙春辉,郎需龙,杨艳玲,王秀然,李晓燕,卜昭阳,王兴龙..羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立[J].中国畜牧兽医,2011,38(3):199-203,5.

基金项目

国家转基因新品种培育重大项目(2009ZX08009163B). (2009ZX08009163B)

中国畜牧兽医

OA北大核心CSTPCD

1671-7236

访问量0
|
下载量0
段落导航相关论文