Ivory Catherine P A, Prystajecky Michael, Jobin Christian, Chadee Kris
Faculty of Medicine, Department of Microbiology and Infectious Diseases, University of Calgary Health Sciences Centre, 3330 Hospital Dr. NW, Calgary, Alberta T2N 4N1, Canada.
Infect Immun. 2008 Jan;76(1):289-97. doi: 10.1128/IAI.01217-07. Epub 2007 Nov 5.
Activation of the innate immune system by bacterial DNA and DNA of other invertebrates represents a pathogen recognition mechanism. In this study we investigated macrophage responses to DNA from the intestinal protozoan parasite Entamoeba histolytica. E. histolytica genomic DNA was purified from log-phase trophozoites and tested with the mouse macrophage cell line RAW 264.7. RAW cells treated with E. histolytica DNA demonstrated an increase in levels of tumor necrosis factor alpha (TNF-alpha) mRNA and protein production. TNF-alpha production was blocked by pretreatment with chloroquine or monensin. In fact, an NF-kappaB luciferase reporter assay in HEK cells transfected with human TLR9 demonstrated that E. histolytica DNA signaled through Toll-like receptor 9 (TLR9) in a manner similar to that seen with CpG-ODN. Immunofluorescence assays confirmed NF-kappaB activation in RAW cells, as seen by nuclear translocation of the p65 subunit. Western blot analysis demonstrated mitogen-activated protein kinase activation by E. histolytica DNA. E. histolytica DNA effects were abolished in MYD88-/- mouse-derived macrophages. In the context of disease, immunization with E. histolytica DNA protected gerbils from an E. histolytica challenge infection. Taken together, these results demonstrate that E. histolytica DNA is recognized by TLR9 to activate macrophages and may provide an innate defense mechanism characterized by the induction of the inflammatory mediator TNF-alpha.
细菌DNA和其他无脊椎动物的DNA激活先天免疫系统代表了一种病原体识别机制。在本研究中,我们调查了巨噬细胞对肠道原生动物寄生虫溶组织内阿米巴DNA的反应。从对数期滋养体中纯化溶组织内阿米巴基因组DNA,并用小鼠巨噬细胞系RAW 264.7进行测试。用溶组织内阿米巴DNA处理的RAW细胞显示肿瘤坏死因子α(TNF-α)mRNA水平和蛋白产生增加。用氯喹或莫能菌素预处理可阻断TNF-α的产生。事实上,在用人类TLR9转染的HEK细胞中进行的NF-κB荧光素酶报告基因检测表明,溶组织内阿米巴DNA通过Toll样受体9(TLR9)发出信号,其方式与用CpG-ODN观察到的相似。免疫荧光检测证实了RAW细胞中NF-κB的激活,如p65亚基的核转位所示。蛋白质印迹分析表明溶组织内阿米巴DNA可激活丝裂原活化蛋白激酶。在源自MYD88-/-小鼠的巨噬细胞中,溶组织内阿米巴DNA的作用被消除。在疾病背景下,用溶组织内阿米巴DNA免疫可保护沙鼠免受溶组织内阿米巴攻击感染。综上所述,这些结果表明,溶组织内阿米巴DNA被TLR9识别以激活巨噬细胞,并可能提供一种以诱导炎症介质TNF-α为特征的先天防御机制。