Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2002-12-17
pubmed:abstractText
Nitric oxide (NO) is an intracellular and intercellular mediator involved in the modulation of many physiologic and pathologic processes including the regulation of neoangiogenesis. We analyzed the effects of basic fibroblast growth factor (bFGF) on NO production in CHO-K1 cells and the intracellular mechanisms involved. bFGF induces NO production through activation of the endothelial NO synthase (eNOS), causing a subsequent increase in cGMP levels. In most systems, eNOS activation is a Ca(2+)-calmodulin-dependent process. In CHO-K1 cells, NO production by bFGF is Ca(2+) and MAP kinase independent, because it was not reverted by pretreatment with intracellular Ca(2+) chelators or MEK inhibitors. Translocation of the eNOS from the plasma membrane, where it is bound to caveolin 1, to the cytosol is the crucial step in the synthesis of NO. We demonstrate that the cytosolic translocation of eNOS is caused by increased synthesis of ceramide dependent by the bFGF activation of sphingomyelinase. Indeed, in the presence of the sphingomyelinase inhibitors D609 or desipramine, bFGF-dependent NO production is abrogated. To support this evidence we evaluated ceramide concentration using HPLC-electrospray ionization-mass spectrometry in controls and in bFGF-treated cells: after bFGF stimulation, a substantial increase in ceramide levels was observed. These data were further confirmed by the lack of NO production in response to fibroblast growth factor in fibroblasts derived from Niemann Pick patients who genetically lack the enzyme sphingomyelinase. In conclusion, ceramide in CHO-K1 cells is responsible for a novel Ca(2+)/calmodulin-independent mechanism for eNOS activation after fibroblast growth factor stimulation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Bridged Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Ceramides, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic GMP, http://linkedlifedata.com/resource/pubmed/chemical/Desipramine, http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 2, http://linkedlifedata.com/resource/pubmed/chemical/NOS3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type III, http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Thiones, http://linkedlifedata.com/resource/pubmed/chemical/tricyclodecane-9-yl-xanthogenate
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0077-8923
pubmed:author
pubmed:issnType
Print
pubmed:volume
973
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
94-104
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12485842-Animals, pubmed-meshheading:12485842-Bridged Compounds, pubmed-meshheading:12485842-CHO Cells, pubmed-meshheading:12485842-Cells, Cultured, pubmed-meshheading:12485842-Ceramides, pubmed-meshheading:12485842-Cricetinae, pubmed-meshheading:12485842-Cyclic GMP, pubmed-meshheading:12485842-Desipramine, pubmed-meshheading:12485842-Enzyme Activation, pubmed-meshheading:12485842-Fibroblast Growth Factor 2, pubmed-meshheading:12485842-Fibroblasts, pubmed-meshheading:12485842-Humans, pubmed-meshheading:12485842-Kinetics, pubmed-meshheading:12485842-Niemann-Pick Diseases, pubmed-meshheading:12485842-Nitric Oxide, pubmed-meshheading:12485842-Nitric Oxide Synthase, pubmed-meshheading:12485842-Nitric Oxide Synthase Type III, pubmed-meshheading:12485842-Phosphodiesterase Inhibitors, pubmed-meshheading:12485842-Reference Values, pubmed-meshheading:12485842-Thiones
pubmed:year
2002
pubmed:articleTitle
Nitric oxide production stimulated by the basic fibroblast growth factor requires the synthesis of ceramide.
pubmed:affiliation
Pharmacology and Neuroscience, National Institute for Cancer Research (IST), c/o Advanced Biotechnology Center (CBA), 16132 Genoa, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't