Source:http://linkedlifedata.com/resource/pubmed/id/10353535
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1999-8-3
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pubmed:abstractText |
Although it is well recognized that interferon-gamma (IFN-gamma) is involved in the development of systemic inflammatory response syndrome, a condition characterized by loss of endothelial barrier function, whether or not IFN-gamma has any direct effect on endothelial cell (EC) death is unclear. Furthermore, which signal transduction pathway involved in IFN-gamma-induced EC apoptosis remains to be elucidated. To answer these questions, we investigated the effect of IFN-gamma on EC death (apoptosis versus necrosis) and the underlying signal transduction pathway responsible for IFN-gamma-induced EC apoptosis. IFN-gamma resulted in a dose-dependent increase in EC apoptosis after 24 h incubation (p < .05). However, IFN-gamma did not induce EC necrosis. Tumor necrosis factor-alpha (TNF-alpha), but not lipopolysaccharide (LPS), had a augmentative effect on IFN-gamma-induced EC apoptosis (p < .05), while both of them alone failed to induce EC apoptosis. These results indicate that exposure of EC to IFN-gamma can cause apoptosis rather than necrosis. Both calcium ionophore, A23187, and the protein kinase C (PKC) activator phorbol-myristate-acetate (PMA) had a synergistic effect on IFN-gamma-induced EC apoptosis (p < .05). However, neither the calcium chelator 1,2-bis 2-aminophenoxy ethane-N,N,N',N'-tetraacetic acid (BAPTA), nor the PKC inhibitor 1 -5-isoquinolinysulfonyl 2-methyl piperazine (H-7) attenuated IFN-gamma-induced EC apoptosis. Three specific tyrosine protein kinase (TPK) inhibitors, herbimycin A, tyrphostin, and genistein, significantly inhibited IFN-gamma-induced EC apoptosis in a dose-dependent fashion (p < .05). Furthermore, the activation of TPK in EC by IFN-gamma was completely abrogated by these TPK inhibitors. These findings suggest that the signal transduction pathway required for induction of EC apoptosis by IFN-gamma is TPK dependent and is independent of calcium and PKC.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcimycin,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Ionophores,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1073-2322
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
311-8
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10353535-Adult,
pubmed-meshheading:10353535-Aged,
pubmed-meshheading:10353535-Apoptosis,
pubmed-meshheading:10353535-Calcimycin,
pubmed-meshheading:10353535-Calcium,
pubmed-meshheading:10353535-Cells, Cultured,
pubmed-meshheading:10353535-Endothelium, Vascular,
pubmed-meshheading:10353535-Enzyme Activation,
pubmed-meshheading:10353535-Humans,
pubmed-meshheading:10353535-Interferon-gamma,
pubmed-meshheading:10353535-Ionophores,
pubmed-meshheading:10353535-Middle Aged,
pubmed-meshheading:10353535-Necrosis,
pubmed-meshheading:10353535-Protein Kinase C,
pubmed-meshheading:10353535-Protein-Tyrosine Kinases,
pubmed-meshheading:10353535-Signal Transduction
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pubmed:year |
1999
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pubmed:articleTitle |
Involvement of tyrosine protein kinase in IFN-gamma-induced human endothelial cell apoptosis.
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pubmed:affiliation |
The Royal College of Surgeons in Ireland, Department of Surgery, Beaumont Hospital, Dublin.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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