Ragno S, Estrada-Garcia I, Butler R, Colston M J
Division of Mycobacterial Research, National Institute for Medical Research, London NW7 1AA, United Kingdom.
Infect Immun. 1998 Aug;66(8):3952-8. doi: 10.1128/IAI.66.8.3952-3958.1998.
We have investigated changes in gene expression in mouse peritoneal macrophages following infection with virulent Mycobacterium tuberculosis. Using differential-display reverse transcription-PCR (RT-PCR), we have identified a gene that was markedly down-regulated within 6 h of infection and remained so for the duration of the experiment (5 days). On sequencing, this gene was found to encode the murine cytochrome c oxidase subunit VIIc (COX VIIc). Down-regulation of COX VIIc during M. tuberculosis infection was confirmed by three independent techniques: limiting-dilution RT-PCR, RNase protection assay, and Northern analysis. Limiting-dilution RT-PCR and Northern analysis were also used to analyze the specificity of this regulation; heat-killed M. tuberculosis, Mycobacterium bovis BCG, and latex beads had no effect on expression of COX VIIc. Down-regulation of this enzyme was also confirmed by using adherent cells isolated from spleens of M. tuberculosis-infected mice. These ex vivo macrophages showed apoptotic features, suggesting a possible involvement of cytochrome c oxidase in the programmed cell death of the host cells.
我们研究了感染强毒力结核分枝杆菌后小鼠腹腔巨噬细胞中的基因表达变化。利用差异显示逆转录聚合酶链反应(RT-PCR),我们鉴定出一个在感染后6小时内显著下调且在实验期间(5天)一直保持下调的基因。测序结果表明,该基因编码小鼠细胞色素c氧化酶亚基VIIc(COX VIIc)。通过三种独立技术证实了结核分枝杆菌感染期间COX VIIc的下调:有限稀释RT-PCR、核糖核酸酶保护分析和Northern印迹分析。有限稀释RT-PCR和Northern印迹分析还用于分析这种调节的特异性;热灭活的结核分枝杆菌、牛分枝杆菌卡介苗和乳胶珠对COX VIIc的表达没有影响。使用从感染结核分枝杆菌的小鼠脾脏中分离的贴壁细胞也证实了这种酶的下调。这些体外巨噬细胞表现出凋亡特征,表明细胞色素c氧化酶可能参与宿主细胞的程序性细胞死亡。