中华皮肤科杂志 ›› 2014, Vol. 47 ›› Issue (3): 186-191.

• 论著 • 上一篇    下一篇

分枝杆菌感染肉芽肿体外模型的建立和验证

田蔚蔚1,张晓东2,王秋玲2,唐美育2,沈建平3,3,王洪生3,王千秋3   

  1. 1. 江西省皮肤病专科医院
    2. 中国医学科学院北京协和医学院皮肤病研究所
    3. 南京 中国医学科学院北京协和医学院皮肤病研究所
  • 收稿日期:2013-05-24 修回日期:2013-09-10 发布日期:2014-03-01
  • 通讯作者: 王千秋 E-mail:doctorwqq@163.com
  • 基金资助:
    国家自然科学基金;北京协和医学院研究生创新基金

Development and validation of an in vitro model of mycobacterial granuloma

  • Received:2013-05-24 Revised:2013-09-10 Published:2014-03-01
  • Supported by:
    ;Graduate Innovation Fund of Peking Union Medical College

摘要: 【摘要】 目的 构建可用于分枝杆菌感染肉芽肿研究的体外模型。 方法 采用人免疫细胞分别与分枝杆菌(海鱼杆菌、结核杆菌、卡介苗及麻风杆菌)共培养的方法构建分枝杆菌感染肉芽肿体外模型,显微镜下动态观察肉芽肿的体外形成过程,并用流式细胞仪检测不同时期细胞表面抗原分子表达,实时定量PCR法检测细胞因子的mRNA表达及ELISA法检测重要细胞因子的分泌等。 结果 共培养7 ~ 9 d后观察到与肉芽肿结构相似的细胞聚集团块,部分细胞形成多核巨细胞;CD14、CD68、CD80等巨噬细胞表面抗原在不同的分枝杆菌组均有阳性表达;肿瘤坏死因子α、干扰素γ、白介素1β、白介素10亦有不同程度的mRNA表达及分泌。结论 初步构建了人分枝杆菌肉芽肿体外模型,为研究分枝杆菌感染过程中肉芽肿形成和免疫反应诱导提供条件。

关键词: 肉芽肿, 分枝杆菌属, 免疫

Abstract: Tian Weiwei, Zhang Xiaodong, Wang Qiuling, Tang Meiyu, Shen Jianping, Wang Hongsheng, Wang Qianqiu. Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China Corresponding authors: Wang Hongsheng, Email: whs33@vip.sina.com; Wang Qianqiu, Email: wangqq@ncstdlc.org 【Abstract】 Objective To establish an in vitro model of mycobacterial granuloma. Methods Mononuclear cells were isolated from peripheral blood of healthy human subjects, and stimulated to differentiate into macrophages, which were then classified into four groups to be cocultured with Mycobacterium marinum, Mycobacterium tuberculosis, Bacillus Calmette-Guérin, and Mycobacterium leprae, respectively, for five days followed by incubation with peripheral blood mononuclear cells (PBMCs) from the corresponding donors to establish an in vitro model of mycobacterial granuloma. The macrophages cocultured with PBMCs or mycobacteria alone served as the control. Microscopy was performed to dynamically visualize the formation of granuloma in vitro, flow cytometry to detect the expressions of cell surface antigens at different stages, real-time quantitative PCR and enzyme-linked immunosorbent assay (ELISA) to determine the mRNA expressions of important cytokines and their protein levels in the supernatant of macrophages, respectively. Results After 7 - 9 days of coculture with mycobacteria and PBMCs, the macrophages aggregated to form granuloma-like clumps, and some cells fused to form multinuclear giant cells, along with the expressions of some surface antigens such as CD14, CD68 and CD86 on these macrophages. The mRNA expressions of some important cytokines, including tumor necrosis factor-α, interferon-γ, interleukin (IL)-1β and IL-10, were detectable in the macrophages cocultured with mycobacteria and PBMCs, and the secretion of these cytokines was confirmed by ELISA in the supernatant of these cells. Conclusions An in vitro model of mycobacterial granuloma is basically established, which may facilitate the investigation into the formation of granuloma caused by and immune response to mycobacterial infection.

Key words: Granuloma, Mycobacterium, Immunity

引用本文

田蔚蔚 张晓东 王秋玲 唐美育 沈建平 王洪生 王千秋. 分枝杆菌感染肉芽肿体外模型的建立和验证[J]. 中华皮肤科杂志, 2014,47(3):186-191. doi: