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Mol Med Rep ; 8(2): 591-6, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23799615

ABSTRACT

Staphylococcal enterotoxin B (SEB) and α­toxin produced by Staphylococcus aureus (S. aureus) are important in the pathogenesis of diseases. In the present study, we investigated the effects of SEB and α­toxin on ECV304 cells. It was identified that both SEB and α­toxin were capable of inducing the apoptosis of ECV304 cells in a dose­ and time­dependent manner. In addition, SEB and α­toxin were able to induce the expression of TNF­α and the activation of caspase­3 and ­8 in the ECV304 cells. The inhibition of TNF­α (with its neutralizing antibody) and caspase­3 and ­8 [with the corresponding inhibitory peptides; z-N-acetyl-Asp-Glu-Val-Asp-aminomethyl-coumarin (DEVD)-fluoromethyl ketone (FMK) for inhibition of caspase­3 and z-N-acetyl-Ile-Glu-Thr-Asp (IETD)-FMK) for inhibition of caspase­8] significantly decreased the rates of cell apoptosis induced by SEB and α­toxin, but was not able to completely block the induced cell apoptosis. These data suggest that SEB and α­toxin induce ECV304 cell apoptosis via a similar mechanism, which is partially mediated by the extrinsic death pathway involving TNF­α and caspase­8. These results provide insights into the synergistic pathogenicity of SEB and α­toxin during S. aureus infection.


Subject(s)
Apoptosis/drug effects , Bacterial Toxins/toxicity , Enterotoxins/toxicity , Hemolysin Proteins/toxicity , Caspase 3/metabolism , Caspase 8/metabolism , Cell Line , Dose-Response Relationship, Drug , Enzyme Activation/drug effects , Staphylococcus aureus , Tumor Necrosis Factor-alpha/metabolism
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