Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105; and.
Integrated Biomedical Sciences Program, University of Tennessee Health Science Center, Memphis, TN 38163.
J Immunol. 2018 Dec 15;201(12):3662-3668. doi: 10.4049/jimmunol.1800788. Epub 2018 Nov 7.
The DNA sensor absent in melanoma 2 (AIM2) forms an inflammasome complex with ASC and caspase-1 in response to subspecies infection, leading to maturation of IL-1β and IL-18 and pyroptosis. AIM2 is critical for host protection against infection in vivo; however, the role of pyroptosis downstream of the AIM2 inflammasome is unknown. Recent studies have identified gasdermin D (GSDMD) as the molecule executing pyroptosis by forming pores on the plasma membrane following activation by inflammatory caspase-1 and -11. In this study, we report that GSDMD-deficient mice were susceptible to infection compared with wild type mice. Interestingly, we observed that GSDMD is required for optimal caspase-1 activation and pyroptotic cell death in -infected bone marrow-derived macrophages. Furthermore, caspase-1 activation was compromised in bone marrow-derived macrophages lacking GSDMD stimulated with other AIM2 inflammasome triggers, including poly(dA:dT) transfection and mouse CMV infection. Overall, our study highlights a function, to our knowledge previously unknown, for GSDMD in promoting caspase-1 activation by AIM2 inflammasome.
黑色素瘤缺失 2 型(AIM2)DNA 传感器在亚属感染时与 ASC 和半胱天冬酶-1 形成炎性体复合物,导致 IL-1β 和 IL-18 的成熟和细胞焦亡。AIM2 对于宿主抵御体内感染至关重要;然而,AIM2 炎性体下游的细胞焦亡作用尚不清楚。最近的研究表明,gasdermin D(GSDMD)是在被炎症性半胱天冬酶-1 和 -11 激活后在质膜上形成孔,从而执行细胞焦亡的分子。在这项研究中,我们报告说,与野生型小鼠相比,GSDMD 缺陷型小鼠易感染。有趣的是,我们观察到 GSDMD 是 - 感染的骨髓来源巨噬细胞中最佳半胱天冬酶-1 激活和细胞焦亡所必需的。此外,缺乏 GSDMD 的骨髓来源巨噬细胞在受到其他 AIM2 炎性体触发物(包括 poly(dA:dT) 转染和鼠 CMV 感染)刺激时,半胱天冬酶-1 激活受到损害。总的来说,我们的研究强调了 GSDMD 在促进 AIM2 炎性体中半胱天冬酶-1 激活方面的功能,这是我们迄今为止未知的。