Stepwise phosphorylation of p65 promotes NF-kappa B activation and NK cell responses during target cell recognition

Abstract

NF-kappa B is a key transcription factor that dictates the outcome of diverse immune responses. How NF-kappa B is regulated by multiple activating receptors that are engaged during natural killer (NK)-target cell contact remains undefined. Here we show that sole engagement of NKG2D, 2B4 or DNAM-1 is insufficient for NF-kappa B activation. Rather, cooperation between these receptors is required at the level of Vav1 for synergistic NF-kappa B activation. Vav1-dependent synergistic signalling requires a separate PI3K-Akt signal, primarily mediated by NKG2D or DNAM-1, for optimal p65 phosphorylation and NF-kappa B activation. Vav1 controls downstream p65 phosphorylation and NF-kappa B activation. Synergistic signalling is defective in X-linked lymphoproliferative disease (XLP1) NK cells entailing 2B4 dysfunction and required for p65 phosphorylation by PI3K-Akt signal, suggesting stepwise signalling checkpoint for NF-kappa B activation. Thus, our study provides a framework explaining how signals from different activating receptors are coordinated to determine specificity and magnitude of NF-kappa B activation and NK cell responses