炎症体
磷酸化
细胞生物学
丝氨酸
激酶
化学
蛋白激酶A
内生
抑制性突触后电位
癌症研究
信号转导
炎症
调节器
机制(生物学)
生物
炎症反应
分泌物
半胱氨酸蛋白酶1
作者
Ruiheng Luo,Mingliang Ma,Dan Wang,Ling Luo,Xueming Xu,Lingmin Huang,Fupeng Wang,Guangyan Kuang,Huiqi Liu,Ruiqing Ni,Xin Li,Qinghua Zhang,Shengfeng Wang,Kai Zhao
标识
DOI:10.1002/advs.202504816
摘要
NLRP3 inflammasome is a multiple protein complex sensing exogenous or endogenous stimuli, and aberrant activation of the NLRP3 inflammasome is implicated in various inflammatory disorders. While numerous small-molecule compounds targeting NLRP3 inflammasome activity have been developed, most have encountered limited success in clinical translation. Through screening of a kinase compound library, GSK461364 is identified as a potent and selective NLRP3 inflammasome inhibitor. Notably, GSK461364 confers significant protective effects in murine models of LPS-induced endotoxemia and DSS-induced colitis. Mechanistic study reveals that GSK461364 exerts its inhibitory effects via targeting Polo-like Kinase 1(PLK1). Specifically, that PLK1-mediated phosphorylation of NEK7, likely occurring at evolutionarily conserved serine residues (Ser221 and Ser260), is shown to enhance NEK7-NLRP3 binding, a critical step for NLRP3 inflammasome assembly. These findings not only establish GSK461364 as a novel therapeutic candidate for NLRP3-driven inflammatory diseases but also provide new insights into the regulatory mechanisms governing inflammasome activation through post-translational modification.
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