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http://purl.uniprot.org/citations/36400933http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36400933http://www.w3.org/2000/01/rdf-schema#comment"Brown adipose tissue (BAT) activity contributes to cardiovascular health by its energy-dissipating capacity but how BAT modulates vascular function and atherosclerosis through endocrine mechanisms remains poorly understood. Here we show that BAT-derived neuregulin-4 (Nrg4) ameliorates atherosclerosis in mice. BAT-specific Nrg4 deficiency accelerates vascular inflammation and adhesion responses, endothelial dysfunction and apoptosis and atherosclerosis in male mice. BAT-specific Nrg4 restoration alleviates vascular inflammation and adhesion responses, attenuates leukocyte homing and reduces endothelial injury and atherosclerosis in male mice. In endothelial cells, Nrg4 decreases apoptosis, inflammation and adhesion responses induced by oxidized low-density lipoprotein. Mechanistically, protein kinase B (Akt)-nuclear factor-κB signaling is involved in the beneficial effects of Nrg4 on the endothelium. Taken together, the results reveal Nrg4 as a potential cross-talk factor between BAT and arteries that may serve as a target for atherosclerosis."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.org/dc/terms/identifier"doi:10.1038/s42255-022-00671-0"xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Cheng Y."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Li Y."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Xu J."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Xu X."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Zhang J.'"xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Xiang L."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Tong J."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Shi L."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"He K."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Meng B."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Xiang G."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/author"Xiang L.'"xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/name"Nat Metab"xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/pages"1573-1590"xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/title"Brown adipose tissue-derived Nrg4 alleviates endothelial inflammation and atherosclerosis in male mice."xsd:string
http://purl.uniprot.org/citations/36400933http://purl.uniprot.org/core/volume"4"xsd:string
http://purl.uniprot.org/citations/36400933http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36400933
http://purl.uniprot.org/citations/36400933http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36400933
http://purl.uniprot.org/uniprot/#_I6L9B2-mappedCitation-36400933http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36400933
http://purl.uniprot.org/uniprot/#_Q9WTX4-mappedCitation-36400933http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36400933