首页> 外文期刊>The Journal of Experomental Medicine >Killer Cell Inhibitory Receptor Recognition of Human Leukocyte Antigen (HLA) Class I Blocks Formation of a pp36/PLC-γ Signaling Complex in Human Natural Killer (NK) Cells
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Killer Cell Inhibitory Receptor Recognition of Human Leukocyte Antigen (HLA) Class I Blocks Formation of a pp36/PLC-γ Signaling Complex in Human Natural Killer (NK) Cells

机译:人类白细胞抗原(HLA)I类的杀伤细胞抑制受体识别可阻止人类自然杀伤(NK)细胞中pp36 /PLC-γ信号复合物的形成。

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The killer cell inhibitory receptors (KIR) of human natural killer (NK) cells recognize human leukocyte antigen class I molecules and inhibit NK cell cytotoxicity through their interaction with protein tyrosine phosphatases (PTP). Here, we report that KIR recognition of class I ligands inhibits distal signaling events and ultimately NK cell cytotoxicity by blocking the association of an adaptor protein (pp36) with phospholipase C-γ in NK cells. In addition, we demonstrate that pp36 can serve as a substrate in vitro for the KIR-associated PTP, PTP-1C (also called SHP-1), and that recognition of class I partially disrupts tyrosine phosphorylation of NK cell proteins, providing evidence for KIR-induced phosphatase activity.
机译:人类自然杀伤(NK)细胞的杀伤细胞抑制受体(KIR)识别人白细胞抗原I类分子,并通过与蛋白质酪氨酸磷酸酶(PTP)相互作用来抑制NK细胞的细胞毒性。在这里,我们报告说,KIR识别I类配体可通过阻断NK细胞中适配器蛋白(pp36)与磷脂酶C-γ的结合来抑制远端信号传导事件并最终抑制NK细胞的细胞毒性。此外,我们证明pp36可以作为KIR相关PTP,PTP-1C(也称为SHP-1)的体外底物,并且对I类的识别会部分破坏NK细胞蛋白的酪氨酸磷酸化,从而为KIR诱导的磷酸酶活性。

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