rdf:type |
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lifeskim:mentions |
umls-concept:C0003483,
umls-concept:C0010853,
umls-concept:C0016026,
umls-concept:C0031621,
umls-concept:C0031669,
umls-concept:C0031670,
umls-concept:C0031672,
umls-concept:C0041485,
umls-concept:C0225336,
umls-concept:C1135183,
umls-concept:C1514873,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636
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pubmed:dateCreated |
2000-4-12
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pubmed:abstractText |
Fibroblast growth factor-mediated signalling was studied in porcine aortic endothelial cells expressing either wild-type fibroblast growth factor receptor-1 or a mutant receptor (Y766F) unable to bind phospholipase C-(&ggr;). Stimulation of cells expressing the wild-type receptor resulted in activation of phospholipases C, D and A(2) and increased phosphoinositide 3-kinase activity. Stimulation of the wild-type receptor also resulted in stress fibre formation and a cellular shape change. Cells expressing the Y766F mutant receptor failed to stimulate phospholipase C, D and A(2) as well as phosphoinositide 3-kinase. Furthermore, no stress fibre formation or shape change was observed. Both the wild-type and Y766F receptor mutant activated MAP kinase and elicited proliferative responses in the porcine aortic endothelial cells. Thus, fibroblast growth factor receptor-1 mediated activation of phospholipases C, D and A(2) and phosphoinositide 3-kinase was dependent on tyrosine 766. Furthermore, whilst tyrosine 766 was not required for a proliferative response, it was required for fibroblast growth factor receptor-1 mediated cytoskeletal reorganisation.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Phospholipase D,
http://linkedlifedata.com/resource/pubmed/chemical/Phospholipases,
http://linkedlifedata.com/resource/pubmed/chemical/Phospholipases A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor Protein-Tyrosine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Fibroblast Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Type C Phospholipases,
http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0021-9533
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
113 ( Pt 4)
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
643-51
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10652257-Animals,
pubmed-meshheading:10652257-Aorta,
pubmed-meshheading:10652257-Cell Division,
pubmed-meshheading:10652257-Cells, Cultured,
pubmed-meshheading:10652257-Cytoskeleton,
pubmed-meshheading:10652257-Endothelium, Vascular,
pubmed-meshheading:10652257-Mitogen-Activated Protein Kinases,
pubmed-meshheading:10652257-Mutagenesis,
pubmed-meshheading:10652257-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:10652257-Phospholipase D,
pubmed-meshheading:10652257-Phospholipases,
pubmed-meshheading:10652257-Phospholipases A,
pubmed-meshheading:10652257-Phosphorylation,
pubmed-meshheading:10652257-Receptor, Fibroblast Growth Factor, Type 1,
pubmed-meshheading:10652257-Receptor Protein-Tyrosine Kinases,
pubmed-meshheading:10652257-Receptors, Fibroblast Growth Factor,
pubmed-meshheading:10652257-Signal Transduction,
pubmed-meshheading:10652257-Swine,
pubmed-meshheading:10652257-Transfection,
pubmed-meshheading:10652257-Type C Phospholipases,
pubmed-meshheading:10652257-Tyrosine
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pubmed:year |
2000
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pubmed:articleTitle |
Tyrosine 766 in the fibroblast growth factor receptor-1 is required for FGF-stimulation of phospholipase C, phospholipase D, phospholipase A(2), phosphoinositide 3-kinase and cytoskeletal reorganisation in porcine aortic endothelial cells.
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pubmed:affiliation |
Department of Genetics, Rudbeck Laboratory, S-75185 Uppsala, Sweden. michael.cross@genpat.uu.se
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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