RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7528218http://www.w3.org/2000/01/rdf-schema#comment"The B cell-specific cell surface molecule CD19 plays a role in regulating immunoglobulin (Ig) receptor signaling, and cross-linking CD19 activates several signaling molecules in mature human B cells. In surface Ig-negative B cell precursors, a protein tyrosine kinase (PTK)-dependent homotypic aggregation response can be triggered by cross-linking CD19. In the current study, we examined the outcome of PTK-mediated signal transduction following CD19 cross-linking on surface Ig negative and surface Ig positive B cell lines, as well as freshly isolated surface Ig-negative B cell precursors. PTK activation resulted in the tyrosine phosphorylation of multiple protein substrates and peaked at 0.5-1 min following CD19 cross-linking in all B-lineage cells examined. One of the tyrosine-phosphorylated substrates was identified as the hematopoietic-specific protein Vav, a guanine nucleotide exchange factor that activates the Ras pathway. Evidence consistent with Ras pathway activation was also demonstrated by MEK activation and subsequent phosphorylation of a MAP kinase fusion protein. CD19 cross-linking, sequential immunoprecipitation, and Western blotting revealed that: (a) Vav becomes associated with CD19, (b) phosphatidylinositol 3-kinase (PI 3-kinase) becomes associated with CD19, and (c) PI 3-kinase becomes associated with Vav. No such physical interaction occurred following control IgG1 cross-linking or cross-linking of class I major histocompatability complex cell surface molecules. Coupled with a previous report (Tuveson, D.A., Carter, R.H., Soltoff, S.P., and Fearon, D.T. (1993) Science 260, 986-988), our data support a model in which CD19 cross-linking induces the formation of a signaling complex that leads to the activation of two pathways involving Ras and PI 3-kinase."xsd:string
http://purl.uniprot.org/citations/7528218http://purl.org/dc/terms/identifier"doi:10.1016/s0021-9258(18)31664-8"xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/author"LeBien T.W."xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/author"Jarvis L."xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/author"Weng W.K."xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/name"J Biol Chem"xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/pages"32514-32521"xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/title"Signaling through CD19 activates Vav/mitogen-activated protein kinase pathway and induces formation of a CD19/Vav/phosphatidylinositol 3-kinase complex in human B cell precursors."xsd:string
http://purl.uniprot.org/citations/7528218http://purl.uniprot.org/core/volume"269"xsd:string
http://purl.uniprot.org/citations/7528218http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7528218
http://purl.uniprot.org/citations/7528218http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7528218
http://purl.uniprot.org/uniprot/#_P15391-mappedCitation-7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/#_O00329-mappedCitation-7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/#_P27986-mappedCitation-7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/#_P15498-mappedCitation-7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/#_P62993-mappedCitation-7528218http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/P15391http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/P15498http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/O00329http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/P27986http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7528218
http://purl.uniprot.org/uniprot/P62993http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7528218