IFI16 senses DNA forms of the lentiviral replication cycle and controls HIV-1 replication

IFI16 感知慢病毒复制周期的 DNA 形式并控制 HIV-1 复制

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作者:Martin R Jakobsen, Rasmus O Bak, Annika Andersen, Randi K Berg, Søren B Jensen, Jin Tengchuan, Anders Laustsen, Kathrine Hansen, Lars Ostergaard, Katherine A Fitzgerald, T Sam Xiao, Jacob G Mikkelsen, Trine H Mogensen, Søren R Paludan

Abstract

Replication of lentiviruses generates different DNA forms, including RNA:DNA hybrids, ssDNA, and dsDNA. Nucleic acids stimulate innate immune responses, and pattern recognition receptors detecting dsDNA have been identified. However, sensors for ssDNA have not been reported, and the ability of RNA:DNA hybrids to stimulate innate immune responses is controversial. Using ssDNAs derived from HIV-1 proviral DNA, we report that this DNA form potently induces the expression of IFNs in primary human macrophages. This response was stimulated by stem regions in the DNA structure and was dependent on IFN-inducible protein 16 (IFI16), which bound immunostimulatory DNA directly and activated the stimulator of IFN genes -TANK-binding kinase 1 - IFN regulatory factors 3/7 (STING-TBK1-IRF3/7) pathway. Importantly, IFI16 colocalized and associated with lentiviral DNA in the cytoplasm in macrophages, and IFI16 knockdown in this cell type augmented lentiviral transduction and also HIV-1 replication. Thus, IFI16 is a sensor for DNA forms produced during the lentiviral replication cycle and regulates HIV-1 replication in macrophages.

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