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September 16, 2025Advanced Science6 citationsOpen Access

GSK461364 Inhibits NLRP3 Inflammasome by Targeting NEK7 Phosphorylation

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RLRuiheng LuoMMMingliang MaDWDan Wang

Key Points

  • GSK461364 significantly inhibits NLRP3 inflammasome activity, promoting protective effects in murine models of endotoxemia.
  • NLRP3 inflammasome assembly is enhanced by PLK1-mediated phosphorylation of NEK7, crucial for inflammation regulation.
  • This study employed a kinase compound library screening to identify GSK461364 as a potent NLRP3 inflammasome inhibitor.
  • Findings emphasize the importance of targeting NEK7 phosphorylation in treating NLRP3-driven inflammatory diseases.

Abstract

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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Cite This Study

Luo et al. (2025) studied this question.

synapsesocial.com/papers/68d44f8331b076d99fa571fbhttps://doi.org/10.1002/advs.202504816
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