韦莉, 金齐力, 管俊昌, 孔晓明. 产单核细胞李斯特菌感染小鼠脾脏树突状细胞亚群和表型的变化[J]. 蚌埠医科大学学报, 2013, 37(6): 645-647,651.
    引用本文: 韦莉, 金齐力, 管俊昌, 孔晓明. 产单核细胞李斯特菌感染小鼠脾脏树突状细胞亚群和表型的变化[J]. 蚌埠医科大学学报, 2013, 37(6): 645-647,651.
    WEI Li, JIN Qi-li, GUAN Jun-chang, KONG Xiao-ming. Differential involvement of dendritic cell subsets during Listeria monocytogenes infection[J]. Journal of Bengbu Medical University, 2013, 37(6): 645-647,651.
    Citation: WEI Li, JIN Qi-li, GUAN Jun-chang, KONG Xiao-ming. Differential involvement of dendritic cell subsets during Listeria monocytogenes infection[J]. Journal of Bengbu Medical University, 2013, 37(6): 645-647,651.

    产单核细胞李斯特菌感染小鼠脾脏树突状细胞亚群和表型的变化

    Differential involvement of dendritic cell subsets during Listeria monocytogenes infection

    • 摘要: 目的:利用产单核细胞李斯特菌(LM)感染BALB/c小鼠模型,研究LM感染对小鼠脾脏树突状细胞(DC)亚群及表型变化的影响。方法:LM尾静脉感染BALB/c小鼠,感染后第3、5、7天取小鼠脾脏,平板稀释法进行脾脏细菌载量分析;流式细胞术检测脾脏DC亚群及DC相关表面分子CD80、CD86的表达情况。结果:感染小鼠脾脏细菌载量感染后第3天有高水平的菌落形成单位计数,随着时间的推移细菌的数量迅速降低,直到第7天基本被清除;CD11c+DC的数量在感染第5天高于对照组(P0.05),CD4+DC的数量在感染后第5天和第7天均高于对照组(P0.05),CD8+DC的数量在感染后第3、5和7天及CD4-CD8-DC的数量在感染后的第3和第5天亦均高于对照组(P0.05~P0.01);LM感染后,DC表面CD80和CD86的表达增加,均于感染后第3天和第5天显著高于对照组(P0.01)。结论:LM感染早期,小鼠脾脏DC亚群出现的增殖和成熟表型特征性分子表达上调,决定了其在细胞免疫应答活化中的作用地位。

       

      Abstract: Objective:To investigate the relative contributions of dendritic cell(DC)in the development of protective immunity to Listeria monocytogenes(LM).Methods:DC subpopulation and phenotype characteristics during early infection of LM were examined.The BALB/c mice were infected by intravenously injection of 2 105LM.Spleen cell suspension was prepared from the mice sacrificed on days 3,5,7 post infection(p.i.).Diluted homogenates in sterile PBS were plated on LB plates to quantify bacterial load in spleen.The percentages of DC subsets,as well as surface molecule CD80 or CD86 expressed on spleen DC were determined by flow cytometry. Results:The overall number of CD4 -CD8+ 、CD4+CD8- and CD4-CD8- DC in the spleen increased significantly after infection with LM.The increases were approximate 1.5-fold augment in the CD4+DC by day 7,and an approximate 3-fold augment in the CD4-CD8+ and CD4-CD8- DC by day 5.The expression of CD80 and CD86 were significantly increased on days 3-5 p.i.and reached its peak on day 3 p.i.for BALB/c mice.Conclusions:These data provide new insight into the relative abundance and function of distinct CD11c-expressing populations during the early stage of LM infection.

       

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