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http://purl.uniprot.org/citations/17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17475851http://www.w3.org/2000/01/rdf-schema#comment"The absence of B7-2-mediated costimulation protects NOD mice from the development of diabetes. Although the effects of B7-2 on T cell priming are well known, its impact on the function of APCs is not fully elucidated. We tested APC function and survival in mice lacking B7-2. A significant reduction in the phagocytic ability was observed in both splenic and pancreatic lymph node-associated dendritic cells (DCs) in B7-2 knockout (KO) mice. DCs from B7-2KO mice exhibited enhanced susceptibility to death, which was reflected by their reduced total cell numbers. Phenotypic analysis of APCs in B7-2KO mice revealed a significantly decreased proportion of CD8alpha+CD205+ DCs. Interestingly, an enhanced proportion of B7-H1+ and B7-DC+ DCs were observed in B7-2KO mice. Lastly, we found that B7-2 deficiency significantly diminished the PKC-epsilon response in APCs upon CD28-Ig stimulation. In conclusion our data suggests that B7-2 promotes the generation of a mature APC repertoire and promotes APC function and survival."xsd:string
http://purl.uniprot.org/citations/17475851http://purl.org/dc/terms/identifier"doi:10.4049/jimmunol.178.10.6236"xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/author"Sarvetnick N."xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/author"Yadav D."xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/name"J Immunol"xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/pages"6236-6241"xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/title"B7-2 regulates survival, phenotype, and function of APCs."xsd:string
http://purl.uniprot.org/citations/17475851http://purl.uniprot.org/core/volume"178"xsd:string
http://purl.uniprot.org/citations/17475851http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17475851
http://purl.uniprot.org/citations/17475851http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17475851
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http://purl.uniprot.org/uniprot/#_P42082-mappedCitation-17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/#_Q3TDR5-mappedCitation-17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/#_Q549Q9-mappedCitation-17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17475851
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http://purl.uniprot.org/uniprot/#_Q61238-mappedCitation-17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/#_Q91YV7-mappedCitation-17475851http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/Q3T9F8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/Q61238http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17475851
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http://purl.uniprot.org/uniprot/A0A0X9RAD7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/P42082http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17475851
http://purl.uniprot.org/uniprot/Q549Q9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17475851