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http://purl.uniprot.org/citations/27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27001958http://www.w3.org/2000/01/rdf-schema#comment"Previously we have shown that transcription factor Foxp1 plays an essential role in maintaining naive T cell quiescence; in the absence of Foxp1, mature naive CD8(+) T cells proliferate in direct response to homeostatic cytokine IL-7. In this study, we report that the deletion of Foxp1 in naive CD8(+) T cells leads to enhanced activation of the PI3K/Akt/mammalian target of rapamycin signaling pathway and its downstream cell growth and metabolism targets in response to IL-7. We found that Foxp1 directly regulates PI3K interacting protein 1, a negative regulator of PI3K. Additionally, we found that deletion of Foxp1 in naive CD8(+) T cells results in increased expression levels of E2fs, the critical components for cell cycle progression and proliferation, in a manner that is not associated with increased phosphorylation of retinoblastoma protein. Taken together, our studies suggest that Foxp1 enforces naive CD8(+) T cell quiescence by simultaneously repressing key pathways in both cellular metabolism and cell cycle progression."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.org/dc/terms/identifier"doi:10.4049/jimmunol.1501896"xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Geng J."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Hu H."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Liu Z."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Wang H."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Wei H."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Yao M."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Wang Y.H."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Shi B."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Sprout S.L."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/author"Stevens A.C."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/name"J Immunol"xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/pages"3537-3541"xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/title"Cutting Edge: Foxp1 Controls Naive CD8+ T Cell Quiescence by Simultaneously Repressing Key Pathways in Cellular Metabolism and Cell Cycle Progression."xsd:string
http://purl.uniprot.org/citations/27001958http://purl.uniprot.org/core/volume"196"xsd:string
http://purl.uniprot.org/citations/27001958http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27001958
http://purl.uniprot.org/citations/27001958http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27001958
http://purl.uniprot.org/uniprot/#_A0A0R4J282-mappedCitation-27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27001958
http://purl.uniprot.org/uniprot/#_A0A0R4J1H9-mappedCitation-27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27001958
http://purl.uniprot.org/uniprot/#_D3Z6Q3-mappedCitation-27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27001958
http://purl.uniprot.org/uniprot/#_H3BJ24-mappedCitation-27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27001958
http://purl.uniprot.org/uniprot/#_P58462-mappedCitation-27001958http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27001958