RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/30738250http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30738250http://www.w3.org/2000/01/rdf-schema#comment"The maintenance of intestinal tissue homeostasis is vital for the resistance against inflammatory bowel diseases (IBDs). Necroptosis is identified as an alternative mode of regulated cell death, which plays a pivotal role in tissue homeostasis. Thus, the roles of RIP3-mediated necroptosis in intestinal inflammation have been extensively studied. However, the biological implications of the mixed lineage kinase-like protein (MLKL), a molecule downstream of RIP3 in gut remain unclear. In this study, the role of MLKL in DSS-induced colitis was examined, and the contribution of gut microbiota was also determined. Compared with non-littermate WT mice, the survival rate, clinical score, intestinal damage and intestinal mucosal barrier integrity of non-littermate MLKL-deficient mice are significantly improved. MLKL deficiency prevents inflammatory cytokines production and MAPK signaling activation. Hence, MLKL deficiency inhibits DSS-induced colitis. Moreover, we proved that DSS susceptibility difference between two genotypes is not driven by intestinal microbiota based on the co-housing of two non-littermate genotypes and qPCR detection of fecal dominant bacterial taxa."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.org/dc/terms/identifier"doi:10.1016/j.molimm.2019.01.018"xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Chen W."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Hu G.Q."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Yang Y.J."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Qin D."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Qin X.X."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/author"Du C.T."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/name"Mol Immunol"xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/pages"132-141"xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/title"MLKL deficiency inhibits DSS-induced colitis independent of intestinal microbiota."xsd:string
http://purl.uniprot.org/citations/30738250http://purl.uniprot.org/core/volume"107"xsd:string
http://purl.uniprot.org/citations/30738250http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30738250
http://purl.uniprot.org/citations/30738250http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30738250
http://purl.uniprot.org/uniprot/#_D3YV42-mappedCitation-30738250http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30738250
http://purl.uniprot.org/uniprot/#_Q9D2Y4-mappedCitation-30738250http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30738250
http://purl.uniprot.org/uniprot/D3YV42http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30738250
http://purl.uniprot.org/uniprot/Q9D2Y4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30738250