<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Guan Q</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Pyroptosis is an important inflammatory form of cell death and &lt;i>Mycobacterium tuberculosis&lt;/i> (&lt;i>M.tb&lt;/i>) chronic infection triggers excessive inflammatory pyroptosis of macrophages. Our previous research has confirmed that a small compound pyrvinium pamoate (PP) could inhibit inflammatory pathological changes and mycobacterial burden in &lt;i>M.tb&lt;/i>-infected mice, but the potential mechanism of PP for inhibiting &lt;i>M.tb&lt;/i>-induced inflammation remains unexplored.&lt;h4>Methods&lt;/h4>The effects of PP on the NLRP3-ASC-Casp1 inflammasome assembly and activation, gasdermin D (GSDMD) mediated pyroptosis and inflammatory cytokines expression were assessed in human THP-1-derived macrophages after &lt;i>M.tb&lt;/i> H37Rv/H37Ra/ &lt;i>Salmonella typhimurium&lt;/i> (&lt;i>S. typhimurium&lt;/i>)</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1553093</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11906677</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Suppression of NLRP3 inflammasome by a small molecule targeting CK1α-β-catenin-NF-κB and CK1α-NRF2-mitochondrial OXPHOS pathways during mycobacterial infection.</pubmed_title><pmcid>PMC11906677</pmcid><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Nie Q</pubmed_authors><pubmed_authors>Guan Q</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Song X</pubmed_authors><pubmed_authors>Zhang XL</pubmed_authors><pubmed_authors>Guang Y</pubmed_authors><pubmed_authors>Xiong H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Suppression of NLRP3 inflammasome by a small molecule targeting CK1α-β-catenin-NF-κB and CK1α-NRF2-mitochondrial OXPHOS pathways during mycobacterial infection.</name><description>&lt;h4>Introduction&lt;/h4>Pyroptosis is an important inflammatory form of cell death and &lt;i>Mycobacterium tuberculosis&lt;/i> (&lt;i>M.tb&lt;/i>) chronic infection triggers excessive inflammatory pyroptosis of macrophages. Our previous research has confirmed that a small compound pyrvinium pamoate (PP) could inhibit inflammatory pathological changes and mycobacterial burden in &lt;i>M.tb&lt;/i>-infected mice, but the potential mechanism of PP for inhibiting &lt;i>M.tb&lt;/i>-induced inflammation remains unexplored.&lt;h4>Methods&lt;/h4>The effects of PP on the NLRP3-ASC-Casp1 inflammasome assembly and activation, gasdermin D (GSDMD) mediated pyroptosis and inflammatory cytokines expression were assessed in human THP-1-derived macrophages after &lt;i>M.tb&lt;/i> H37Rv/H37Ra/ &lt;i>Salmonella typhimurium&lt;/i> (&lt;i>S. typhimurium&lt;/i>)</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-04-20T00:08:06.737Z</modification><creation>2025-04-20T00:08:06.737Z</creation></dates><accession>S-EPMC11906677</accession><cross_references><pubmed>40092991</pubmed><doi>10.3389/fimmu.2025.1553093</doi></cross_references></HashMap>