Description:
<jats:title>Abstract</jats:title><jats:p>NK cells are innate immune cells characterized by their ability to spontaneously lyse tumor and virally infected cells. We have recently demonstrated that IL‐15‐sufficient DC regulate NK cell effector functions in mice. Here, we established that among ITAM‐proximal signaling molecules, the expression levels of the scaffold molecule Linker for Activation of T cells (LAT) and its transcription factor ELF‐1 were reduced 4 days after in vivo depletion of DC. Addition of IL‐15, a cytokine presented by DC to NK cells, regulates LAT expression in NK cells with a significant effect on the DNAM1<jats:sup>+</jats:sup> subset compared to DNAM1<jats:sup>−</jats:sup> cells. We also found that LAT expression is regulated via interaction of the DNAM1 receptor with its ligand CD155 in both immature and mature NK cells, independently of NK cell education. Finally, we found that LAT expression within DNAM1<jats:sup>+</jats:sup> NK cells might be responsible for enhanced calcium mobilization following the triggering of activating receptors on NK cells. Altogether, we found that LAT expression is tightly regulated in DNAM1<jats:sup>+</jats:sup> NK cells, via interaction(s) with DC, which express CD155 and IL‐15, resulting in rapid activation of the DNAM1<jats:sup>+</jats:sup> subset during activating receptor triggering.</jats:p>