Department of Immunology, University of Washington School of Medicine, 750 Republican St., Seattle, WA 98109, USA.
Center for Innate Immunity and Immune Disease, University of Washington School of Medicine, 750 Republican St., Seattle, WA 98109, USA.
Sci Immunol. 2020 Jan 24;5(43). doi: 10.1126/sciimmunol.aba4219.
Detection of intracellular DNA by the cGAS-STING pathway activates a type I interferon-mediated innate immune response that protects from virus infection. Whether there are additional DNA sensing pathways, and how such pathways might function, remains controversial. We show here that humans-but not laboratory mice-have a second, potent, STING-independent DNA sensing pathway (SIDSP). We identify human DNA-dependent protein kinase (DNA-PK) as the sensor of this pathway and demonstrate that DNA-PK activity drives a robust and broad antiviral response. We show that the E1A oncoprotein of human adenovirus 5 and the ICP0 protein of herpes simplex virus 1 block this response. We found heat shock protein HSPA8/HSC70 as a target for inducible phosphorylation in the DNA-PK antiviral pathway. Last, we demonstrate that DNA damage and detection of foreign DNA trigger distinct modalities of DNA-PK activity. These findings reveal the existence, sensor, a specific downstream target, and viral antagonists of a SIDSP in human cells.
cGAS-STING 通路检测细胞内 DNA 会激活 I 型干扰素介导的先天免疫反应,从而防止病毒感染。是否存在其他 DNA 感应途径,以及这些途径如何发挥作用,仍然存在争议。我们在这里表明,人类——而不是实验小鼠——具有第二种强大的、不依赖于 STING 的 DNA 感应途径(SIDSP)。我们鉴定出人源 DNA 依赖性蛋白激酶(DNA-PK)是该途径的传感器,并证明 DNA-PK 活性可驱动强大且广泛的抗病毒反应。我们表明,人腺病毒 5 的 E1A 癌蛋白和单纯疱疹病毒 1 的 ICP0 蛋白可阻断该反应。我们发现热休克蛋白 HSPA8/HSC70 是 DNA-PK 抗病毒途径中可诱导磷酸化的靶标。最后,我们证明 DNA 损伤和外源 DNA 的检测会触发 DNA-PK 活性的不同模式。这些发现揭示了人细胞中 SIDSP 的存在、传感器、特定下游靶标和病毒拮抗剂。