Biological responses, including those occurring during immune responses, must be controlled by signals that turn them on, as well as signals that turn them off. In addition, fine-tuning can be achieved through signals that amplify or downmodulate responses. The complexity in signal transduction pathways that regulate these responses is daunting. Even terminal responses, such as degranulation by effector cells in the immune system, do not follow a simple one-way signaling pathway. The required initial protein tyrosine phosphorylation events are rapidly reversed by dephosphorylation, and the depleted calcium stores are replenished. Unless the effector cell undergoes programmed cell death after activation, it returns to a basal state of activation from where it can be activated again. Negative regulation of effector cell function is sometimes very tight, such that cellular activation is prevented altogether. This type of inhibitory control is an essential feature of natural killer (NK) cells. Unlike cytotoxic T cells that kill target cells upon a recognition event mediated by their antigen-specific receptors, NK cells are triggered to kill target cells by interactions between activating NK receptors and ligands that are expressed fairly ubiquitously on target cells. The specificity in target cell recognition is achieved primarily by inhibitory receptors specific for MHC class I molecules.KeywordsNatural Killer CellInhibitory ReceptorCytoplasmic TailActivate Natural Killer CellMurine Natural Killer CellThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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