RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/12406903http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12406903http://www.w3.org/2000/01/rdf-schema#comment"The regulation of cell death in activated naive T cells is not well understood. We examined the expression of A1, an antiapoptotic member of the Bcl-2 family, following activation of naive mouse splenocytes. A1 gene expression was strongly but transiently induced during the first day of activation, with a peak at 2 to 6 hours, whereas Bcl-2 mRNA was simultaneously transiently down-regulated. Transgenic (Tg) overexpression of A1-a in T cells via the lck distal promoter resulted in decreased apoptosis following activation either with concanavalin A or with antibodies to CD3 and CD28 and led to a doubling of T-cell yield by 5 days. Tg A1-a also partially protected thymocytes from several proapoptotic stimuli but did not protect T-cell blasts from cell death induced by reactivation via the T-cell receptor. Tg Bcl-2 and Tg A1-a showed a similar ability to reduce apoptosis in both resting and activated T cells. However, in activated splenocyte cultures, the increase in 5-day T-cell yield observed with Tg Bcl-2 was only half that produced by Tg A1-a. This difference could be attributed at least in part to the fact that A1, unlike Bcl-2, did not inhibit S-phase entry of activated cells. The A1 protein may represent an adaptation of the Bcl-2 gene family to the need for survival regulation in the context of a proliferative stimulus."xsd:string
http://purl.uniprot.org/citations/12406903http://purl.org/dc/terms/identifier"doi:10.1182/blood-2002-04-1229"xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/author"Gonzalez J."xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/author"Orlofsky A."xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/author"Prystowsky M.B."xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/pages"2679-2685"xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/title"A1 is a growth-permissive antiapoptotic factor mediating postactivation survival in T cells."xsd:string
http://purl.uniprot.org/citations/12406903http://purl.uniprot.org/core/volume"101"xsd:string
http://purl.uniprot.org/citations/12406903http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12406903
http://purl.uniprot.org/citations/12406903http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12406903
http://purl.uniprot.org/uniprot/#_Q8BY26-mappedCitation-12406903http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12406903
http://purl.uniprot.org/uniprot/#_Q3TKD1-mappedCitation-12406903http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12406903
http://purl.uniprot.org/uniprot/#_Q8R323-mappedCitation-12406903http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12406903
http://purl.uniprot.org/uniprot/Q8BY26http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12406903
http://purl.uniprot.org/uniprot/Q3TKD1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12406903
http://purl.uniprot.org/uniprot/Q8R323http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12406903