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http://purl.uniprot.org/citations/33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33594251http://www.w3.org/2000/01/rdf-schema#comment"The mucosa microenvironment is critical for intestinal stem cell self-renewal and reconstruction of the epithelial barrier in inflammatory bowel disease (IBD), where the mechanisms underlying cross-talk between intestinal crypts and the microenvironment remain unclear. Here, we firstly identified miR-494-3p as an important protector in colitis. miR-494-3p levels were decreased and negatively correlated with the severity in human IBD samples, as well as in colitis mice. In colitis crypts, a notable cytokine-cytokine receptor, miR-494-3p-targeted EDA2R and the ligand EDA-A2, suppressed colonic stemness and epithelial repair by inhibiting β-catenin/c-Myc. In differentiated IECs, miR-494-3p inhibits macrophage recruitment, M1 activation and EDA-A2 secretion by targeting IKKβ/NF-κB in colitis. A miR-494-3p agomir system notably ameliorated the severity of colonic colitis in vivo. Collectively, our findings uncover a miR-494-3p-mediated cross-talk mechanism by which macrophage-induced intestinal stem cell impairment aggravates intestinal inflammation."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.org/dc/terms/identifier"doi:10.1038/s42003-021-01730-0"xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Gao H."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Liu Z."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Lu L."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Lin R."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Lu H."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Sun X."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Song L."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Xu X."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Chang R."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/author"Zhan L."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/name"Commun Biol"xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/pages"213"xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/title"Macrophage-derived EDA-A2 inhibits intestinal stem cells by targeting miR-494/EDA2R/beta-catenin signaling in mice."xsd:string
http://purl.uniprot.org/citations/33594251http://purl.uniprot.org/core/volume"4"xsd:string
http://purl.uniprot.org/citations/33594251http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33594251
http://purl.uniprot.org/citations/33594251http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33594251
http://purl.uniprot.org/uniprot/#_Q1L2D6-mappedCitation-33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33594251
http://purl.uniprot.org/uniprot/#_Q1L2D8-mappedCitation-33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33594251
http://purl.uniprot.org/uniprot/#_Q1L2D9-mappedCitation-33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33594251
http://purl.uniprot.org/uniprot/#_Q1L2E0-mappedCitation-33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33594251
http://purl.uniprot.org/uniprot/#_A0A0U5J8Q0-mappedCitation-33594251http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33594251