Burshtyn D N, Scharenberg A M, Wagtmann N, Rajagopalan S, Berrada K, Yi T, Kinet J P, Long E O
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Immunity. 1996 Jan;4(1):77-85. doi: 10.1016/s1074-7613(00)80300-3.
Cytolysis of target cells by natural killer (NK) cells and by some cytotoxic T cells occurs unless prevented by inhibitory receptors that recognize MHC class I on target cells. Human NK cells express a p58 inhibitory receptor specific for HLA-C. We report association of the tyrosine phosphatase HCP with the p58 receptor in NK cells. HCP association was dependent on tyrosine phosphorylation of p58. Phosphotyrosyl peptides corresponding to the p58 tail bound and activated HCP in vitro. Furthermore, introduction of an inactive mutant HCP into an NK cell line prevented the p58-mediated inhibition of target cell lysis. These data imply that the inhibitory function of p58 is dependent on its tyrosine phosphorylation and on recruitment and activation of HCP.
自然杀伤(NK)细胞和某些细胞毒性T细胞对靶细胞的细胞溶解作用会发生,除非被识别靶细胞上MHC I类分子的抑制性受体所阻止。人类NK细胞表达一种对HLA - C特异的p58抑制性受体。我们报告了酪氨酸磷酸酶HCP与NK细胞中p58受体的关联。HCP的关联依赖于p58的酪氨酸磷酸化。对应于p58尾部的磷酸酪氨酸肽在体外结合并激活HCP。此外,将无活性的突变型HCP导入NK细胞系可阻止p58介导的靶细胞裂解抑制。这些数据表明p58的抑制功能依赖于其酪氨酸磷酸化以及HCP的募集和激活。