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http://purl.uniprot.org/citations/24489101http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24489101http://www.w3.org/2000/01/rdf-schema#comment"The accumulation of improperly folded proteins within the endoplasmic reticulum (ER) generates perturbations known as ER stress that engage the unfolded protein response. ER stress is involved in many inflammatory pathologies that are also associated with the production of the proinflammatory cytokine IL-1β. In this study, we demonstrate that macrophages undergoing ER stress are able to drive the production and processing of pro-IL-1β in response to LPS stimulation in vitro. Interestingly, the classical NLRP3 inflammasome is dispensable, because maturation of pro-IL-1β occurs normally in the absence of the adaptor protein ASC. In contrast, processing of pro-IL-1β is fully dependent on caspase-8. Intriguingly, we found that neither the unfolded protein response transcription factors XBP1 and CHOP nor the TLR4 adaptor molecule MyD88 is necessary for caspase-8 activation. Instead, both caspase activation and IL-1β production require the alternative TLR4 adaptor TRIF. This pathway may contribute to IL-1-driven tissue pathology in certain disease settings."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.org/dc/terms/identifier"doi:10.4049/jimmunol.1302549"xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Sher A."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Cerundolo V."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Fitzgerald P."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Green D.R."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Dillon C.P."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Mayer-Barber K.D."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Hieny S."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Oberst A."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Yip R."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Shenderov K."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Riteau N."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/author"Oland S."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/name"J Immunol"xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/pages"2029-2033"xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/title"Cutting edge: Endoplasmic reticulum stress licenses macrophages to produce mature IL-1beta in response to TLR4 stimulation through a caspase-8- and TRIF-dependent pathway."xsd:string
http://purl.uniprot.org/citations/24489101http://purl.uniprot.org/core/volume"192"xsd:string
http://purl.uniprot.org/citations/24489101http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24489101
http://purl.uniprot.org/citations/24489101http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24489101
http://purl.uniprot.org/uniprot/#_A0A087WQT6-mappedCitation-24489101http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24489101
http://purl.uniprot.org/uniprot/#_D3YX14-mappedCitation-24489101http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24489101
http://purl.uniprot.org/uniprot/#_E9PZP3-mappedCitation-24489101http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24489101