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Gasdermin D 促进 AIM2 炎性小体的激活,并对宿主抵抗 至关重要。

Gasdermin D Promotes AIM2 Inflammasome Activation and Is Required for Host Protection against .

机构信息

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.

出版信息

J Immunol. 2018 Dec 15;201(12):3662-3668. doi: 10.4049/jimmunol.1800788. Epub 2018 Nov 7.

DOI:10.4049/jimmunol.1800788
PMID:30404813
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6317867/
Abstract

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.

摘要

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。

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Detrimental Type I Interferon Signaling Dominates Protective AIM2 Inflammasome Responses during Francisella novicida Infection.弗朗西斯菌属 novicida 感染期间,Ⅰ型干扰素信号通路抑制 AIM2 炎性小体的保护性反应。
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ASC- and caspase-8-dependent apoptotic pathway diverges from the NLRC4 inflammasome in macrophages.
细胞焦亡:分子机制及其在疾病中的作用
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Interferon signalling and non-canonical inflammasome activation promote host protection against multidrug-resistant Acinetobacter baumannii.干扰素信号转导和非经典炎性小体激活促进宿主抵抗多药耐药鲍曼不动杆菌。
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Carbon monoxide-releasing molecule-3 ameliorates traumatic brain injury-induced cardiac dysfunctions via inhibition of pyroptosis and apoptosis.一氧化碳释放分子-3通过抑制细胞焦亡和凋亡改善创伤性脑损伤诱导的心脏功能障碍。
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