From the Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
J Biol Chem. 2014 Mar 28;289(13):9146-57. doi: 10.1074/jbc.M113.534321. Epub 2014 Feb 14.
Interferon regulatory factor (IRF) family members have been implicated as critical transcription factors that function in immune responses, hematopoietic differentiation, and cell growth regulation. Activation of IRF5 results in the production of pro-inflammatory cytokines such as TNFα, IL6, and IL12, as well as type I interferons. In this study, we demonstrate that HIV-2 Vpx interacts with IRF5, and Vpx inhibits IRF5-mediated transactivation. Expression of Vpx in THP-1 cells reduced mRNA levels and protein production of Toll-like receptor-dependent IL6, IL12p40, and TNFα induced by lipopolysaccharide, R848, and ODN2216. Chromatin immunoprecipitation assays show that Vpx expression results in decreased promoter binding activity of IRF5. This study provides new insights into mechanisms employed by HIV-2 to counteract innate immune defenses against viral infection.
干扰素调节因子 (IRF) 家族成员被认为是在免疫反应、造血分化和细胞生长调节中起关键作用的转录因子。IRF5 的激活导致促炎细胞因子如 TNFα、IL6 和 IL12 以及 I 型干扰素的产生。在这项研究中,我们证明 HIV-2 的 Vpx 与 IRF5 相互作用,并且 Vpx 抑制 IRF5 介导的转录激活。在 THP-1 细胞中表达 Vpx 会降低脂多糖、R848 和 ODN2216 诱导的 Toll 样受体依赖性 IL6、IL12p40 和 TNFα 的 mRNA 水平和蛋白产生。染色质免疫沉淀分析表明,Vpx 的表达导致 IRF5 启动子结合活性降低。这项研究为 HIV-2 用来对抗病毒感染的先天免疫防御的机制提供了新的见解。