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http://purl.uniprot.org/citations/31231034http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31231034http://www.w3.org/2000/01/rdf-schema#comment"Tissue-resident macrophages require specific milieus for the maintenance of defining gene-expression programs. Expression of the transcription factor GATA6 is required for the homeostasis, function and localization of peritoneal cavity-resident macrophages. Gata6 expression is maintained in a non-cell autonomous manner and is elicited by the vitamin A metabolite, retinoic acid. Here, we found that the GATA6 transcriptional program is a common feature of macrophages residing in all visceral body cavities. Retinoic acid-dependent and -independent hallmark genes of GATA6+ macrophages were induced by mesothelial and fibroblastic stromal cells that express the transcription factor Wilms' Tumor 1 (WT1), which drives the expression of two rate-limiting enzymes in retinol metabolism. Depletion of Wt1+ stromal cells reduced the frequency of GATA6+ macrophages in the peritoneal, pleural and pericardial cavities. Thus, Wt1+ mesothelial and fibroblastic stromal cells constitute essential niche components supporting the tissue-specifying transcriptional landscape and homeostasis of cavity-resident macrophages."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.org/dc/terms/identifier"doi:10.1016/j.immuni.2019.05.010"xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Li Q."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Sandoval W."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Harris C.A."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Kim K.W."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Cooper J.E."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Junttila M.R."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Turley S.J."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Randolph G.J."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Buechler M.B."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Williams J.W."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Little C.C."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Dominguez C.X."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/author"Onufer E.J."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/name"Immunity"xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/pages"119-130.e5"xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/title"A Stromal Niche Defined by Expression of the Transcription Factor WT1 Mediates Programming and Homeostasis of Cavity-Resident Macrophages."xsd:string
http://purl.uniprot.org/citations/31231034http://purl.uniprot.org/core/volume"51"xsd:string
http://purl.uniprot.org/citations/31231034http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31231034
http://purl.uniprot.org/citations/31231034http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31231034
http://purl.uniprot.org/uniprot/#_A0A0G2JGF4-mappedCitation-31231034http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31231034
http://purl.uniprot.org/uniprot/#_A0A077S2U6-mappedCitation-31231034http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31231034