Cell Reports · 2016 · 139 citations · 50 references
Life SciencesImmunologyMolecular BiologyCell AdhesionInnate ImmunitySignal TransductionCell Adhesion ReceptorsImmune RegulationNatural Killer Cell BiologyNatural Killer Cell DevelopmentNatural Killer Cell FunctionNatural Killer Cell RegulationCell ActivationDisease-causing VariantsNatural Cytotoxicity ReceptorsNatural Killer Cell CytotoxicityNatural Killer Cell Effector FunctionsNatural Killer Cell Inhibitory SignalingNatural Killer Cell Receptor InteractionsNatural Killer Cell Receptor-ligand Interactions
Natural killer (NK) cells possess potent cytotoxic mechanisms that need to be tightly controlled. Here, we explored the regulation and function of GPR56/ADGRG1, an adhesion G protein-coupled receptor implicated in developmental processes and expressed distinctively in mature NK cells. Expression of GPR56 was triggered by Hobit (a homolog of Blimp-1 in T cells) and declined upon cell activation. Through studying NK cells from polymicrogyria patients with disease-causing mutations in ADGRG1, encoding GPR56, and NK-92 cells ectopically expressing the receptor, we found that GPR56 negatively regulates immediate effector functions, including production of inflammatory cytokines and cytolytic proteins, degranulation, and target cell killing. GPR56 pursues this activity by associating with the tetraspanin CD81. We conclude that GPR56 inhibits natural cytotoxicity of human NK cells.
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Regulation of human NK-cell cytokine and chemokine production by target cell recognition
Cyril Fauriat, Eric O. Long, Hans‐Gustaf Ljunggren et al. · Blood · 2009 · 843 citations · Full text
Comparative studies of human FcRIII-positive and negative natural killer cells.
Arnon Nagler, Lewis L. Lanier, Steven E. Cwirla et al. · The Journal of Immunology · 1989 · 683 citations · Full text