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FEBS Lett ; 579(18): 3947-52, 2005 Jul 18.
Article in English | MEDLINE | ID: mdl-16000198

ABSTRACT

Tumor necrosis factor alpha (TNF-alpha) is one of the best-described cell death promoters. In murine L929 fibroblasts, dexamethasone inhibits TNF-alpha-induced cytotoxicity. Since phosphatidyl inositol 3 kinase (PI3K) and nuclear factor kappa B (NF-kappaB) proteins regulate several survival pathways, we evaluated their participation in dexamethasone protection against TNF-alpha cell death. We interfered with these pathways by overexpressing a negative dominant mutant of PI3K or a non-degradable mutant of inhibitor of NF-kappaB alpha (IkappaBalpha) (the cytoplasmic inhibitor of NF-kappaB) in L929 cells. The mutant IkappaB, but not the mutant PI3K, abrogated dexamethasone-mediated protection. The loss of dexamethasone protection was associated with a diminished accumulation in XIAP and c-IAP proteins.


Subject(s)
Dexamethasone/pharmacology , NF-kappa B/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Tumor Necrosis Factor-alpha/metabolism , Animals , Blotting, Western , Cell Death , Cell Line , Cell Nucleus/metabolism , Cell Proliferation , Cell Survival , Dexamethasone/chemistry , Dose-Response Relationship, Drug , Down-Regulation , Fibroblasts/metabolism , Glucocorticoids/pharmacology , Inhibitor of Apoptosis Proteins , Mice , Mutation , Plasmids/metabolism , Proteins/metabolism , Signal Transduction , X-Linked Inhibitor of Apoptosis Protein
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