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http://purl.uniprot.org/citations/27523270http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27523270http://www.w3.org/2000/01/rdf-schema#comment"The kinases RIPK1 and RIPK3 and the pseudo-kinase MLKL have been identified as key regulators of the necroptotic cell death pathway, although a role for MLKL within the whole animal has not yet been established. Here, we have shown that MLKL deficiency rescued the embryonic lethality caused by loss of Caspase-8 or FADD. Casp8(-/-)Mlkl(-/-) and Fadd(-/-)Mlkl(-/-) mice were viable and fertile but rapidly developed severe lymphadenopathy, systemic autoimmune disease, and thrombocytopenia. These morbidities occurred more rapidly and with increased severity in Casp8(-/-)Mlkl(-/-) and Fadd(-/-)Mlkl(-/-) mice compared to Casp8(-/-)Ripk3(-/-) or Fadd(-/-)Ripk3(-/-) mice, respectively. These results demonstrate that MLKL is an essential effector of aberrant necroptosis in embryos caused by loss of Caspase-8 or FADD. Furthermore, they suggest that RIPK3 and/or MLKL may exert functions independently of necroptosis. It appears that non-necroptotic functions of RIPK3 contribute to the lymphadenopathy, autoimmunity, and excess cytokine production that occur when FADD or Caspase-8-mediated apoptosis is abrogated."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.org/dc/terms/identifier"doi:10.1016/j.immuni.2016.07.016"xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Lin A."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Green D.R."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Strasser A."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Alexander W.S."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"O'Reilly L.A."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Silke J."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Alvarez-Diaz S."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Dillon C.P."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Tanzer M.C."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Lalaoui N."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Rodriguez D.A."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Josefsson E.C."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Hakem R."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/author"Lebois M."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/name"Immunity"xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/pages"513-526"xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/title"The Pseudokinase MLKL and the Kinase RIPK3 Have Distinct Roles in Autoimmune Disease Caused by Loss of Death-Receptor-Induced Apoptosis."xsd:string
http://purl.uniprot.org/citations/27523270http://purl.uniprot.org/core/volume"45"xsd:string
http://purl.uniprot.org/citations/27523270http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27523270
http://purl.uniprot.org/citations/27523270http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27523270
http://purl.uniprot.org/uniprot/#_A0A087WQT6-mappedCitation-27523270http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27523270