RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7579389http://www.w3.org/2000/01/rdf-schema#comment"We have previously shown that granulocyte-macrophage colony-stimulating factor (GM-CSF) gene expression induced by interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-alpha) in the murine stromal cell line +/+.1-LDA 11 involves activation of phospholipase A2 (PLA2). Furthermore, induction of GM-CSF gene expression due to release of arachidonic acid as a result of PLA2 activation was mediated by the transcriptional factor c-jun. In the present study, we have investigated the potential mechanism involved in the induction of c-jun gene expression by arachidonic acid. Arachidonic acid induced transcription of c-jun mRNA. Downregulation of protein kinase C (PKC) by chronic exposure of stromal cells to the phorbol ester 12-O-tetradecanoyl-phorbol-13-acetate (TPA; 400 nmol/L) did not effect c-jun expression induced by arachidonate. Moreover, pretreatment of cells with the PKC inhibitor, calphostin C (1 mumol/L), caused a marked decrease of c-jun expression induced by TPA, but had no influence on c-jun expression induced by arachidonate. To explore the hypothesis that a tyrosine kinase signalling pathway, independent of PKC activation, was involved in arachidonate-induced c-jun expression, stromal cells were pretreated with the protein tyrosine kinase inhibitor, genistein, before challenge with arachidonic acid. Arachidonate 50 mumol/L)-induced c-jun expression was inhibited, in a dose- and time-dependent manner, by genistein. Genistein similarly inhibited c-jun expression in stromal cells exposed to IL-1 (500 U/mL) plus TNF-alpha (500 U/mL). The potential role of a tyrosine kinase pathway in arachidonate-mediated c-jun expression was further investigated by assaying the tyrosine kinase activity of cells challenged with arachidonic acid, IL-1, and TNF-alpha. Exposure of stromal cells to arachidonic acid induced a 2.1-fold increase in intracellular tyrosine kinase activity determined by phosphorylation of the synthetic peptide, raytide, in the presence of [gamma-32P]-ATP. Similarly, IL-1 and TNF-alpha induced 1.7- and 2.4-fold increases in tyrosine protein kinase activity, respectively. The effect of arachidonic acid on tyrosine kinase activity was inhibited by genistein and was enhanced by sodium vanadate. The increase of protein tyrosine kinase activity detected in arachidonate-stimulated cells was associated, in a dose- and time-dependent fashion, with tyrosine phosphorylation of 240-, 40-, and 29-kD substrates. These results are consistent with the hypothesis that a tyrosine phosphorylation process is triggered by arachidonate as an early event in the signalling pathway that leads to increased expression of c-jun.(ABSTRACT TRUNCATED AT 400 WORDS)"xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/author"Rizzo M.T."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/author"Boswell H.S."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/author"Carlo-Stella C."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/author"Mangoni L."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/author"Rizzoli V."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/date"1995"xsd:gYear
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/pages"2967-2975"xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/title"Arachidonic acid induces c-jun gene expression in stromal cells stimulated by interleukin-1 and tumor necrosis factor-alpha: evidence for a tyrosine-kinase-dependent process."xsd:string
http://purl.uniprot.org/citations/7579389http://purl.uniprot.org/core/volume"86"xsd:string
http://purl.uniprot.org/citations/7579389http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7579389
http://purl.uniprot.org/citations/7579389http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7579389
http://purl.uniprot.org/uniprot/#_A0A0R4J210-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_A0A0U5J4W4-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q3TI17-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q3U0Y6-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q3U593-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q62161-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q52L79-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_Q3V255-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_P01582-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_P10749-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389
http://purl.uniprot.org/uniprot/#_P05627-mappedCitation-7579389http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7579389