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http://purl.uniprot.org/citations/12515814http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12515814http://www.w3.org/2000/01/rdf-schema#comment"Transduction of Tat-tagged fusion proteins confirmed a hypothesis based on pharmacologic inhibitors (Fuortes, M., M. Melchior, H. Han, G.J. Lyon, and C. Nathan. 1999. J. Clin. Invest. 104:327-335) that proline-rich tyrosine kinase (Pyk2) plays a critical role in the activation of adherent human neutrophils, and allowed an analysis of individual Pyk2 domains not possible with chemical inhibitors. Acting as a dominant negative, the COOH terminus of Pyk2 fused to a Tat peptide (Tat-CT), but not other regions of Pyk2, specifically inhibited the respiratory burst of cells responding to tumor necrosis factor (TNF), Salmonella, or Listeria, while sparing responses induced by phorbol ester. Tat-CT suppressed TNF-triggered cell spreading and the phosphorylation of endogenous Pyk2 and the associated tyrosine kinase Syk without blocking the ability of neutrophils to degranulate and kill bacteria. Thus, separate signals control the respiratory burst and degranulation, and a normal rate of killing of some bacteria can be sustained by granule products in conjunction with a minimal residual respiratory burst. Inhibition of select inflammatory functions without impairment of antibacterial activity may commend the Pyk2 pathway as a potential target for antiinflammatory therapy."xsd:string
http://purl.uniprot.org/citations/12515814http://purl.org/dc/terms/identifier"doi:10.1084/jem.20021638"xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/author"Han H."xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/author"Nathan C."xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/author"Fuortes M."xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/name"J Exp Med"xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/pages"63-75"xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/title"Critical role of the carboxyl terminus of proline-rich tyrosine kinase (Pyk2) in the activation of human neutrophils by tumor necrosis factor: separation of signals for the respiratory burst and degranulation."xsd:string
http://purl.uniprot.org/citations/12515814http://purl.uniprot.org/core/volume"197"xsd:string
http://purl.uniprot.org/citations/12515814http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12515814
http://purl.uniprot.org/citations/12515814http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12515814
http://purl.uniprot.org/uniprot/#_Q14289-mappedCitation-12515814http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12515814
http://purl.uniprot.org/uniprot/#_Q6ZRA8-mappedCitation-12515814http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12515814
http://purl.uniprot.org/uniprot/#_Q59GM4-mappedCitation-12515814http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12515814
http://purl.uniprot.org/uniprot/Q6ZRA8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12515814
http://purl.uniprot.org/uniprot/Q14289http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12515814
http://purl.uniprot.org/uniprot/Q59GM4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/12515814