目标2
巨噬细胞
烷基化
化学
体外
半胱氨酸
体内
细胞生物学
生物化学
突变
分子生物学
细胞
癌症研究
共价键
毒性
细胞培养
生物
作用机理
作者
J J,Ying Chen,Pei Wang,Yan Zhang,Yi Li,Qing Tu,Xinru Zhao,Xuanqi Yao,Feng Li,Yuan Yuan,Chenwei Wu,Lin Wang,Yuwei Chen,Chenchen Liu,Rui Kang,Daolin Tang,Liangfang Yao,Fengqian Chen,Jinbao Li
标识
DOI:10.1038/s41423-026-01414-x
摘要
Although the immunometabolite itaconate has long been considered an anti-inflammatory, we found that its profound accumulation paradoxically drives macrophage cell death and pro-inflammatory responses. However, the exact molecular mechanisms underlying itaconate-induced macrophage toxicity remain unclear. Here, we demonstrate that pathophysiologically relevant high concentrations of itaconate covalently alkylate the absent in melanoma 2 (AIM2) protein at the cysteine 113 (C113) residue. Itaconate-mediated C113 alkylation structurally stabilizes the AIM2 protein and triggers a conformational change, enabling it to drive ASC oligomerization, PANoptosome assembly, and subsequent macrophage PANoptosis. Utilizing in vitro lentiviral reconstitution in primary macrophages alongside plasmid-mediated expression in cell lines, we rigorously confirmed that the AIM2 C113A mutation completely abolishes itaconate-induced AIM2 stabilization and PANoptosis. In vivo models further corroborated the pathogenic contribution of this axis to systemic sepsis. Taken together, our findings reveal a novel pro-inflammatory mechanism of itaconate via the post-translational modification of AIM2. The itaconate-AIM2 alkylation axis provides crucial mechanistic insights into macrophage depletion and systemic inflammation, highlighting a potential therapeutic target for severe sepsis.
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