{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["14"],"submitter":["Bierschenk D"],"funding":["Alfred Österlunds Stiftelse","Vetenskapsrådet","Deutsche Forschungsgemeinschaft","Kungliga Fysiografiska Sällskapet i Lund","Anna-Greta Crafoords Stiftelse för Reumatologisk Forskning","Tore Nilsons Stiftelse för Medicinsk Forskning","Magnus Bergvalls Stiftelse"],"pubmed_abstract":["Dysregulated NLRP3 inflammasome activation drives a wide variety of diseases, while endogenous inhibition of this pathway is poorly characterised. The serum protein C4b-binding protein (C4BP) is a well-established inhibitor of complement with emerging functions as an endogenously expressed inhibitor of the NLRP3 inflammasome signalling pathway. Here, we identified that C4BP purified from human plasma is an inhibitor of crystalline- (monosodium urate, MSU) and particulate-induced (silica) NLRP3 inflammasome activation. Using a C4BP mutant panel, we identified that C4BP bound these particles <i>via</i> specific protein domains located on the C4BP α-chain. Plasma-purified C4BP was internalised into MSU- or silica-stimulated human primary macrophages, and inhibited MSU- or silica-induced inflammasome complex assembly and IL-1β cytokine secretion. While internalised C4BP in MSU or silica-stimulated human macrophages was in close proximity to the inflammasome adaptor protein ASC, C4BP had no direct effect on ASC polymerisation in <i>in vitro</i> assays. C4BP was also protective against MSU- and silica-induced lysosomal membrane damage. We further provide evidence for an anti-inflammatory function for C4BP <i>in vivo</i>, as <i>C4bp<sup>-/-</sup></i> mice showed an elevated pro-inflammatory state following intraperitoneal delivery of MSU. Therefore, internalised C4BP is an inhibitor of crystal- or particle-induced inflammasome responses in human primary macrophages, while murine C4BP protects against an enhanced inflammatory state <i>in vivo</i>. Our data suggests C4BP has important functions in retaining tissue homeostasis in both human and mice as an endogenous serum inhibitor of particulate-stimulated inflammasome activation."],"journal":["Frontiers in immunology"],"pagination":["1149822"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10239802"],"repository":["biostudies-literature"],"pubmed_title":["C4b-binding protein inhibits particulate- and crystalline-induced NLRP3 inflammasome activation."],"pmcid":["PMC10239802"],"pubmed_authors":["Blom AM","Eschenburg S","Wetsel RA","Dziedzic M","Bresch IP","Bierschenk D","King BC","Binder CJ","Papac-Milicevic N","Bettoni S","Kovacic V"],"additional_accession":[]},"is_claimable":false,"name":"C4b-binding protein inhibits particulate- and crystalline-induced NLRP3 inflammasome activation.","description":"Dysregulated NLRP3 inflammasome activation drives a wide variety of diseases, while endogenous inhibition of this pathway is poorly characterised. The serum protein C4b-binding protein (C4BP) is a well-established inhibitor of complement with emerging functions as an endogenously expressed inhibitor of the NLRP3 inflammasome signalling pathway. Here, we identified that C4BP purified from human plasma is an inhibitor of crystalline- (monosodium urate, MSU) and particulate-induced (silica) NLRP3 inflammasome activation. Using a C4BP mutant panel, we identified that C4BP bound these particles <i>via</i> specific protein domains located on the C4BP α-chain. Plasma-purified C4BP was internalised into MSU- or silica-stimulated human primary macrophages, and inhibited MSU- or silica-induced inflammasome complex assembly and IL-1β cytokine secretion. While internalised C4BP in MSU or silica-stimulated human macrophages was in close proximity to the inflammasome adaptor protein ASC, C4BP had no direct effect on ASC polymerisation in <i>in vitro</i> assays. C4BP was also protective against MSU- and silica-induced lysosomal membrane damage. We further provide evidence for an anti-inflammatory function for C4BP <i>in vivo</i>, as <i>C4bp<sup>-/-</sup></i> mice showed an elevated pro-inflammatory state following intraperitoneal delivery of MSU. Therefore, internalised C4BP is an inhibitor of crystal- or particle-induced inflammasome responses in human primary macrophages, while murine C4BP protects against an enhanced inflammatory state <i>in vivo</i>. Our data suggests C4BP has important functions in retaining tissue homeostasis in both human and mice as an endogenous serum inhibitor of particulate-stimulated inflammasome activation.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023","modification":"2025-07-03T03:06:58.005Z","creation":"2025-04-19T14:14:18.845Z"},"accession":"S-EPMC10239802","cross_references":{"pubmed":["37283747"],"doi":["10.3389/fimmu.2023.1149822"]}}