Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Animal Resources Center and the Veterinary Pathology Core, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Cell. 2020 Apr 30;181(3):674-687.e13. doi: 10.1016/j.cell.2020.03.040. Epub 2020 Apr 15.
Caspases regulate cell death, immune responses, and homeostasis. Caspase-6 is categorized as an executioner caspase but shows key differences from the other executioners. Overall, little is known about the functions of caspase-6 in biological processes apart from apoptosis. Here, we show that caspase-6 mediates innate immunity and inflammasome activation. Furthermore, we demonstrate that caspase-6 promotes the activation of programmed cell death pathways including pyroptosis, apoptosis, and necroptosis (PANoptosis) and plays an essential role in host defense against influenza A virus (IAV) infection. In addition, caspase-6 promoted the differentiation of alternatively activated macrophages (AAMs). Caspase-6 facilitated the RIP homotypic interaction motif (RHIM)-dependent binding of RIPK3 to ZBP1 via its interaction with RIPK3. Altogether, our findings reveal a vital role for caspase-6 in facilitating ZBP1-mediated inflammasome activation, cell death, and host defense during IAV infection, opening additional avenues for treatment of infectious and autoinflammatory diseases and cancer.
Caspases 调节细胞死亡、免疫反应和体内平衡。Caspase-6 被归类为执行 Caspase,但与其他执行 Caspase 相比表现出关键差异。总的来说,除了细胞凋亡之外,人们对 Caspase-6 在生物学过程中的功能知之甚少。在这里,我们表明 Caspase-6 介导先天免疫和炎症小体激活。此外,我们证明 Caspase-6 促进包括细胞焦亡、细胞凋亡和坏死性凋亡(PANoptosis)在内的程序性细胞死亡途径的激活,并在宿主抵抗流感 A 病毒(IAV)感染方面发挥重要作用。此外,Caspase-6 促进了替代激活的巨噬细胞(AAMs)的分化。Caspase-6 通过与 RIPK3 的相互作用,促进了 RIPK3 与 ZBP1 的 RIP 同源相互作用基序(RHIM)依赖性结合。总之,我们的研究结果揭示了 Caspase-6 在促进 ZBP1 介导的炎症小体激活、细胞死亡和 IAV 感染期间宿主防御中的重要作用,为治疗感染性和自身炎症性疾病以及癌症开辟了新的途径。