<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu J</submitter><funding>NIAID NIH HHS</funding><pagination>eadl2993</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12020992</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(103)</volume><pubmed_abstract>The NLRP3 inflammasome plays a critical role in innate immunity and inflammatory diseases. NIMA-related kinase 7 (NEK7) is essential for inflammasome activation, and its interaction with NLRP3 is enhanced by K&lt;sup>+&lt;/sup> efflux. However, the mechanism by which K&lt;sup>+&lt;/sup> efflux promotes this interaction remains unknown. Here, we show that NEK7 is rapidly phosphorylated at threonine-190/191 by JNK1 downstream of K&lt;sup>+&lt;/sup> efflux and gasdermin D (GSDMD) after NLRP3 activation. NEK7 phosphorylation enhances the binding between NEK7 and NLRP3, which further promotes inflammasome assembly and activation. Mutant mice and macrophages in which Thr&lt;sup>190&lt;/sup> and Thr&lt;sup>191&lt;/sup> of Nek7 were replaced by valine exhibited impaired NEK7 phosphorylation, NLRP3 inflammasome activation, and </pubmed_abstract><journal>Science immunology</journal><pubmed_title>NEK7 phosphorylation amplifies NLRP3 inflammasome activation downstream of potassium efflux and gasdermin D.</pubmed_title><pmcid>PMC12020992</pmcid><funding_grant_id>R01 AI148544</funding_grant_id><funding_grant_id>R37 AI063331</funding_grant_id><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Odeh N</pubmed_authors><pubmed_authors>Nunez G</pubmed_authors><pubmed_authors>Sun F</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Duan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>NEK7 phosphorylation amplifies NLRP3 inflammasome activation downstream of potassium efflux and gasdermin D.</name><description>The NLRP3 inflammasome plays a critical role in innate immunity and inflammatory diseases. NIMA-related kinase 7 (NEK7) is essential for inflammasome activation, and its interaction with NLRP3 is enhanced by K&lt;sup>+&lt;/sup> efflux. However, the mechanism by which K&lt;sup>+&lt;/sup> efflux promotes this interaction remains unknown. Here, we show that NEK7 is rapidly phosphorylated at threonine-190/191 by JNK1 downstream of K&lt;sup>+&lt;/sup> efflux and gasdermin D (GSDMD) after NLRP3 activation. NEK7 phosphorylation enhances the binding between NEK7 and NLRP3, which further promotes inflammasome assembly and activation. Mutant mice and macrophages in which Thr&lt;sup>190&lt;/sup> and Thr&lt;sup>191&lt;/sup> of Nek7 were replaced by valine exhibited impaired NEK7 phosphorylation, NLRP3 inflammasome activation, and </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-06T19:35:52.078Z</modification><creation>2026-06-04T03:11:47.769Z</creation></dates><accession>S-EPMC12020992</accession><cross_references><pubmed>39752537</pubmed><doi>10.1126/sciimmunol.adl2993</doi></cross_references></HashMap>