Blood Cell Development and Function Program, Fox Chase Cancer Center, Philadelphia, PA, 19111, USA.
Department of Microbiology and Immunology, Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Curr Opin Virol. 2021 Dec;51:134-140. doi: 10.1016/j.coviro.2021.10.004. Epub 2021 Oct 21.
Z-DNA Binding protein 1 (ZBP1) activates Receptor Interacting Protein Kinase 3 (RIPK3) -dependent cell death during lytic infection by members of the orthomyxovirus, herpesvirus and poxvirus families. ZBP1 possesses two Zα domains capable of selective binding to Z-DNA, as well as to Z-RNA. We have now unveiled Z-RNA as the ligand that activates ZBP1 in cells infected with orthomyxoviruses (influenza A and B viruses) and the poxvirus vaccinia virus (VACV). Orthomyxovirus Z-RNA is sensed by ZBP1 in the nucleus of infected cells, resulting in nuclear activation of RIPK3, consequent rupture of the nucleus, and hyper-inflammatory 'nuclear necroptosis'. VACV-generated Z-RNA accumulates in the cytoplasm, where it is sequestered from ZBP1 by E3, the viral E3L gene product. In viruses where the E3 Zα domain has been mutated, ZBP1 senses Z-RNA and triggers RIPK3-dependent necroptosis in the cytoplasm. Z-RNA is thus a new viral pathogen-associated molecular pattern (PAMP).
Z-DNA 结合蛋白 1(ZBP1)在正粘病毒、疱疹病毒和痘病毒家族成员的裂解感染过程中激活受体相互作用蛋白激酶 3(RIPK3)依赖性细胞死亡。ZBP1 具有两个 Zα 结构域,能够选择性结合 Z-DNA 和 Z-RNA。我们现在揭示了 Z-RNA 是正粘病毒(甲型和乙型流感病毒)和痘病毒(牛痘病毒)感染细胞中激活 ZBP1 的配体。正粘病毒 Z-RNA 在感染细胞的核内被 ZBP1 识别,导致 RIPK3 的核激活,随后核破裂和过度炎症性“核坏死”。VACV 产生的 Z-RNA 在细胞质中积累,其中它被病毒 E3L 基因产物 E3 的 Zα 结构域隔离。在 E3 Zα 结构域发生突变的病毒中,ZBP1 识别 Z-RNA 并触发 RIPK3 依赖性细胞质坏死。因此,Z-RNA 是一种新的病毒病原体相关分子模式(PAMP)。