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http://purl.uniprot.org/citations/21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21949016http://www.w3.org/2000/01/rdf-schema#comment"Regulatory T cells (Tregs) play a critical role in the immune system to regulate peripheral tolerance and prevent autoimmunity. However, the relative importance of different mechanisms of Treg function remains obscure. In this article, we reveal a limited role for programmed cell death pathways in mediating Treg suppression of conventional T cells. We show that Tregs are able to suppress the proliferation of conventional T cells that are resistant to apoptosis (Bim(-/-), Bim(-/-)Puma(-/-), Bcl-2 transgenic) or receptor-interacting serine-threonine kinase-dependent necrosis (also referred to as regulated necrosis or necroptosis) (Ripk3(-/-)) in several in vitro and in vivo assays. These data suggest that programmed cell death pathways, such as apoptosis and receptor-interacting serine-threonine kinase-dependent necrosis, are not required for Treg-mediated suppression."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.org/dc/terms/identifier"doi:10.4049/jimmunol.1100548"xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/author"Vignali D.A."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/author"Green D.R."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/author"Delgoffe G.M."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/author"Szymczak-Workman A.L."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/name"J Immunol"xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/pages"4416-4420"xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/title"Cutting edge: regulatory T cells do not mediate suppression via programmed cell death pathways."xsd:string
http://purl.uniprot.org/citations/21949016http://purl.uniprot.org/core/volume"187"xsd:string
http://purl.uniprot.org/citations/21949016http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21949016
http://purl.uniprot.org/citations/21949016http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/21949016
http://purl.uniprot.org/uniprot/#_A0A1L4AQQ4-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
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http://purl.uniprot.org/uniprot/#_E9PZP3-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
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http://purl.uniprot.org/uniprot/#_A0A1L4AQQ5-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
http://purl.uniprot.org/uniprot/#_A0A1L4AQQ8-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
http://purl.uniprot.org/uniprot/#_A0A1L4AQR6-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
http://purl.uniprot.org/uniprot/#_A0A2I3BPT3-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
http://purl.uniprot.org/uniprot/#_A0A7I2V3S7-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016
http://purl.uniprot.org/uniprot/#_A0A2I3BQW9-mappedCitation-21949016http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21949016