上睑下垂
细胞生物学
炎症反应
程序性细胞死亡
脂多糖
促炎细胞因子
炎症
细胞因子
肿瘤坏死因子α
坏死
免疫学
细胞
化学
类有机物
细胞凋亡
效应器
劈理(地质)
纳米载体
细胞毒性
巨噬细胞
癌症研究
炎症体
作者
Jianhui Sun,Jun Yang,Jie Tao,Yifan Yang,Rui Wang,Huacai Zhang,Wenyi Liu,Shulin Zhao,Rong Shao,Yuhui He,Shasha Tao,Yaxiong Li,H. Qu,Di Liu,Jingwen Li,Jianxin Jiang,Bo Deng,Chu Gao,Ping Lin,Ling Zeng
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2025-09-15
卷期号:26 (10): 1660-1672
被引量:11
标识
DOI:10.1038/s41590-025-02280-x
摘要
The formation of membrane pores by cleaved N-terminal gasdermin D (GSDMD-NT) results in the release of cytokines and inflammatory cell death, known as pyroptosis. Blocking GSDMD-NT pores is an attractive and promising strategy for mitigating inflammation. Here we demonstrate that SK56, an artificial intelligence-screened peptide, effectively obstructs GSDMD-NT pores and inhibits pyroptosis and cytokine release in macrophages and human peripheral blood leukocyte-induced pyroptosis. SK56 prevents septic death induced by lipopolysaccharide or cecal ligation and puncture surgery in mice. SK56 does not influence cleavage of interleukin-1β or GSDMD. Instead, SK56 inhibits the release of cytokines from pyroptotic macrophages, mitigates the activation of primary mouse dendritic cells triggered by incubation with pyroptotic cytomembranes and prevents widespread cell death of human alveolar organoids in an organoid-macrophage coculture model. SK56 blocks GSDMD-NT pores on lipid-bilayer nanoparticles and enters pyroptotic macrophages to inhibit mitochondrial damage. SK56 presents new therapeutic possibilities for counteracting inflammation, which is implicated in numerous diseases.
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