Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Science. 2013 Aug 23;341(6148):903-6. doi: 10.1126/science.1240933. Epub 2013 Aug 8.
Retroviruses, including HIV, can activate innate immune responses, but the host sensors for retroviruses are largely unknown. Here we show that HIV infection activates cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) synthase (cGAS) to produce cGAMP, which binds to and activates the adaptor protein STING to induce type I interferons and other cytokines. Inhibitors of HIV reverse transcriptase, but not integrase, abrogated interferon-β induction by the virus, suggesting that the reverse-transcribed HIV DNA triggers the innate immune response. Knockout or knockdown of cGAS in mouse or human cell lines blocked cytokine induction by HIV, murine leukemia virus, and simian immunodeficiency virus. These results indicate that cGAS is an innate immune sensor of HIV and other retroviruses.
逆转录病毒,包括 HIV,能够激活先天免疫反应,但宿主对逆转录病毒的传感器在很大程度上尚不清楚。在这里,我们表明 HIV 感染激活环鸟苷酸-腺苷酸(cGAMP)合酶(cGAS)产生 cGAMP,该物质与衔接蛋白 STING 结合并激活诱导 I 型干扰素和其他细胞因子。HIV 逆转录酶的抑制剂,但不是整合酶,消除了病毒诱导的干扰素-β,这表明逆转录的 HIV DNA 引发了先天免疫反应。在小鼠或人类细胞系中敲除或敲低 cGAS 可阻断 HIV、鼠白血病病毒和猴免疫缺陷病毒引起的细胞因子诱导。这些结果表明 cGAS 是 HIV 和其他逆转录病毒的先天免疫传感器。