Tyrosine phosphorylation of a human killer inhibitory receptor recruits protein tyrosine phosphatase 1C.

KS Campbell, M Dessing, M Lopez-Botet… - The Journal of …, 1996 - rupress.org
The Journal of experimental medicine, 1996rupress.org
Natural killer (NK) cells express killer inhibitory receptors that mediate negative regulation of
NK cell cytotoxicity upon binding to MHC class I molecules on target cells. Unrelated
inhibitory receptors on B cells have recently been shown to function through recruitment of
phosphotyrosine phosphatase 1C (PTP-1C). Here, we show that a human killer inhibitory
receptor specific for HLA-C also recruits PTP-1C after phosphorylation induced either by the
pharmacological agent phenylarsine oxide or by conjugation with target cells. This …
Natural killer (NK) cells express killer inhibitory receptors that mediate negative regulation of NK cell cytotoxicity upon binding to MHC class I molecules on target cells. Unrelated inhibitory receptors on B cells have recently been shown to function through recruitment of phosphotyrosine phosphatase 1C (PTP-1C). Here, we show that a human killer inhibitory receptor specific for HLA-C also recruits PTP-1C after phosphorylation induced either by the pharmacological agent phenylarsine oxide or by conjugation with target cells. This recruitment is mediated by the binding of specific cytoplasmic phosphotyrosine-containing sequences to PTP-1C. These results implicate PTP-1C as a cytosolic component of the negative signaling pathway through NK cell inhibitory receptors.
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