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• W2013885821 abstract "NF-κB is a key transcription factor involved in the regulation of T-cell activation and proliferation upon engagement of the T-cell receptor (TCR). T cells that lack the IκB kinase (IKKβ) are unable to activate NF-κB, and rapidly undergo apoptosis upon activation. NF-κB activation following T-cell receptor engagement induces the expression of Mdm2 through interaction with NF-κB sites in its P1 promoter, and enforced expression of Mdm2 protected T cells deficient for NF-κB activation from activation-induced cell death. In T cells with intact NF-κB signaling, ablation or pharmacologic inhibition of Mdm2 resulted in activation-induced apoptosis. Mdm2 coprecipitates with p73 in activated T cells, and apoptosis induced by inhibition of Mdm2 was p73-dependent. Further, Bim was identified as a p73 target gene required for cell death induced by Mdm2 inhibition, and a p73-responsive element in intron 1 of Bim was characterized. Our results demonstrate a pathway for survival of activated T cells through NF-κB–induced Mdm2, which blocks Bim-dependent apoptosis through binding and inhibition of p73." @default.
• W2013885821 created "2016-06-24" @default.
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• W2013885821 date "2010-10-04" @default.
• W2013885821 modified "2023-10-16" @default.
• W2013885821 title "NF-κB inhibits T-cell activation-induced, p73-dependent cell death by induction of MDM2" @default.
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• W2013885821 doi "https://doi.org/10.1073/pnas.1006163107" @default.
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