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http://purl.uniprot.org/citations/22195744http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/22195744http://www.w3.org/2000/01/rdf-schema#comment"To fulfill the bioenergetic and biosynthetic demand of proliferation, T cells reprogram their metabolic pathways from fatty acid β-oxidation and pyruvate oxidation via the TCA cycle to the glycolytic, pentose-phosphate, and glutaminolytic pathways. Two of the top-ranked candidate transcription factors potentially responsible for the activation-induced T cell metabolic transcriptome, HIF1α and Myc, were induced upon T cell activation, but only the acute deletion of Myc markedly inhibited activation-induced glycolysis and glutaminolysis in T cells. Glutamine deprivation compromised activation-induced T cell growth and proliferation, and this was partially replaced by nucleotides and polyamines, implicating glutamine as an important source for biosynthetic precursors in active T cells. Metabolic tracer analysis revealed a Myc-dependent metabolic pathway linking glutaminolysis to the biosynthesis of polyamines. Therefore, a Myc-dependent global metabolic transcriptome drives metabolic reprogramming in activated, primary T lymphocytes. This may represent a general mechanism for metabolic reprogramming under patho-physiological conditions."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.org/dc/terms/identifier"doi:10.1016/j.immuni.2011.09.021"xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Wang R."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Chi H."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Carter R."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Milasta S."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Fitzgerald P."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Finkelstein D."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Green D.R."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Munger J."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Dillon C.P."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"Shi L.Z."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/author"McCormick L.L."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/name"Immunity"xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/pages"871-882"xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/title"The transcription factor Myc controls metabolic reprogramming upon T lymphocyte activation."xsd:string
http://purl.uniprot.org/citations/22195744http://purl.uniprot.org/core/volume"35"xsd:string
http://purl.uniprot.org/citations/22195744http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/22195744
http://purl.uniprot.org/citations/22195744http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/22195744
http://purl.uniprot.org/uniprot/#_A0A0R4J1E9-mappedCitation-22195744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22195744
http://purl.uniprot.org/uniprot/#_A0A0R4J1F0-mappedCitation-22195744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22195744
http://purl.uniprot.org/uniprot/#_E0CZD1-mappedCitation-22195744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22195744
http://purl.uniprot.org/uniprot/#_A0A158SIS7-mappedCitation-22195744http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/22195744