ausblenden:
Schlagwörter:
LMP1; NF-κB; apoptosis; cell death; caspase
Zusammenfassung:
NF-κB is a transcription factor known to promote or antagonize cell death depending on cell types and stimuli. Here, we demonstrate that expression of latent membrane protein 1 (LMP1), an Epstein-Barr virus (EBV)-encoded membrane protein, triggers programmed cell death in an NF-κB-dependent manner. Co-expression of NF-κB inhibitors completely prevented activation of NF-κB and LMP1-induced cell death. Addition therein of RelA, an active subunit of NF-κB, restored the NF-κB activation and cell death induction by LMP1, but RelA alone did not induce cell death. These results indicate that the activation of NF-κB is required for cell death induced by LMP1. Moreover, LMP1 induced activation of caspase-3 via the activation of NF-κB. Studies with z-VAD- fmk, a caspase inhibitor, indicated that NF-κB mediated both caspase-dependent and -independent death pathways. In conclusion, the cell death induced by LMP1 uncovered caspase- dependent and -independent death pathways both of which require NF-κB.
