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化学破坏细胞焦亡孔形成蛋白 gasdermin D 可抑制炎症细胞死亡和脓毒症。

Chemical disruption of the pyroptotic pore-forming protein gasdermin D inhibits inflammatory cell death and sepsis.

机构信息

Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.

出版信息

Sci Immunol. 2018 Aug 24;3(26). doi: 10.1126/sciimmunol.aat2738.

Abstract

Dysregulation of inflammatory cell death is a key driver of many inflammatory diseases. Pyroptosis, a highly inflammatory form of cell death, uses intracellularly generated pores to disrupt electrolyte homeostasis and execute cell death. Gasdermin D, the pore-forming effector protein of pyroptosis, coordinates membrane lysis and the release of highly inflammatory molecules, such as interleukin-1β, which potentiate the overactivation of the innate immune response. However, to date, there is no pharmacologic mechanism to disrupt pyroptosis. Here, we identify necrosulfonamide as a direct chemical inhibitor of gasdermin D, the pyroptotic pore-forming protein, which binds directly to gasdermin D to inhibit pyroptosis. Pharmacologic inhibition of pyroptotic cell death by necrosulfonamide is efficacious in sepsis models and suggests that gasdermin D inhibitors may be efficacious clinically in inflammatory diseases.

摘要

炎症细胞死亡的失调是许多炎症性疾病的关键驱动因素。细胞焦亡是一种高度炎症的细胞死亡形式,它利用细胞内产生的孔来破坏电解质平衡并执行细胞死亡。Gasdermin D 是细胞焦亡的孔形成效应蛋白,协调膜裂解和释放高度炎症分子,如白细胞介素-1β,从而增强先天免疫反应的过度激活。然而,迄今为止,还没有药理学机制来破坏细胞焦亡。在这里,我们确定了邻苯二甲酰亚磺酰胺是一种直接的 Gasdermin D 化学抑制剂,Gasdermin D 是细胞焦亡的孔形成蛋白,它直接与 Gasdermin D 结合以抑制细胞焦亡。邻苯二甲酰亚磺酰胺对细胞焦亡的药理学抑制在败血症模型中是有效的,这表明 Gasdermin D 抑制剂在炎症性疾病的临床治疗中可能是有效的。

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