RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/33104252http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33104252http://www.w3.org/2000/01/rdf-schema#comment"The cathelin-related antimicrobial peptide CRAMP protects the mouse colon from inflammation, inflammation-associated carcinogenesis, and disrupted microbiome balance, as shown in systemic Cnlp-/- mice (also known as Camp-/- mice). However, the mechanistic basis for the role and the cellular source of CRAMP in colon pathophysiology are ill defined. This study, using either epithelial or myeloid conditional Cnlp-/- mice, demonstrated that epithelial cell-derived CRAMP played a major role in supporting normal development of colon crypts, mucus production, and repair of injured mucosa. On the other hand, myeloid cell-derived CRAMP potently supported colon epithelial resistance to bacterial invasion during acute inflammation with exacerbated mucosal damage and higher rate of mouse mortality. Therefore, a well concerted cooperation of epithelial- and myeloid-derived CRAMP is essential for colon mucosal homeostasis. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.org/dc/terms/identifier"doi:10.1002/path.5572"xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Gong W."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Huang J."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Yoshimura T."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Chen K."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Trinchieri G."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Wang J.M."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Yao X."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"McCulloch J."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"O'hUigin C."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Bian X.W."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/author"Dzutsev A.K."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/name"J Pathol"xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/pages"339-350"xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/title"Distinct contributions of cathelin-related antimicrobial peptide (CRAMP) derived from epithelial cells and macrophages to colon mucosal homeostasis."xsd:string
http://purl.uniprot.org/citations/33104252http://purl.uniprot.org/core/volume"253"xsd:string
http://purl.uniprot.org/citations/33104252http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33104252
http://purl.uniprot.org/citations/33104252http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33104252
http://purl.uniprot.org/uniprot/#_A0A077S2U6-mappedCitation-33104252http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33104252
http://purl.uniprot.org/uniprot/#_A0A2I3BPU6-mappedCitation-33104252http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33104252
http://purl.uniprot.org/uniprot/#_O88536-mappedCitation-33104252http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33104252
http://purl.uniprot.org/uniprot/#_Q3TZ97-mappedCitation-33104252http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33104252