Department of Clinical Immunology and Allergology, University Hospital and School of Medicine in Hradec Kralove, Charles University in Prague, 500 05, Hradec Kralove, Czech Republic.
Folia Microbiol (Praha). 2010 Mar;55(2):191-200. doi: 10.1007/s12223-010-0028-3. Epub 2010 May 19.
Mutual interactions were investigated between intracellular parasitic bacterium Francisella tularensis (F.t.; highly virulent bacterium responsible for tularemia, replicating within the host macrophages) and murine macrophage-like cell line J774. Recombinant murine lymphokine INF-gamma and/or LPS derived from E. coli were determined to stimulate in vitro antimicrobial activity of macrophage-like J774 cell line against the live vaccine strain (LVS) of F.t. through their ability to produce proinflammatory cytokines and chemokines. F.t. infection up-regulated IL-12 p40 production and down-regulated TNF-alpha production by stimulated macrophages; on the other hand, F.t. infection did not affect the production of IL-8, IL-6, MCP-5, and RANTES by stimulated macrophages. This showed that F.t. infection modulates the cytokine synthesis by J774 macrophage cell line.
研究了细胞内寄生菌土拉弗朗西斯菌(F.t.;一种高度致病的细菌,可引起土拉热,在宿主巨噬细胞内复制)与鼠源巨噬细胞样细胞系 J774 之间的相互作用。重组鼠源淋巴因子 INF-γ和/或源自大肠杆菌的 LPS 通过产生促炎细胞因子和趋化因子,被确定能够刺激巨噬细胞样 J774 细胞系对活疫苗株(LVS)的体外抗微生物活性。F.t.感染上调了刺激巨噬细胞产生的 IL-12 p40,下调了 TNF-α的产生;另一方面,F.t.感染不影响刺激巨噬细胞产生的 IL-8、IL-6、MCP-5 和 RANTES。这表明 F.t.感染可调节 J774 巨噬细胞系的细胞因子合成。