Association with FcRγ is essential for activation signal through NKR-P1 (CD161) in natural killer (NK) cells and NK1.1+ T cells

被引:134
作者
Arase, N
Arase, H
Park, SY
Ohno, H
Ra, C
Saito, T
机构
[1] Chiba Univ, Sch Med, Ctr Biol Sci, Div Mol Genet,Chuou Ku, Chiba 260, Japan
[2] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 113, Japan
关键词
D O I
10.1084/jem.186.12.1957
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer (NK) cells exhibit cytotoxicity against variety of tumor cells and virus-infected cells without prior sensitization and represent unique lymphocytes involved in primary host defense. NKR-P1 is thought to be one of NK receptors mediating activation signals because cross-linking of NKR-P1 activates NK cells to exhibit cytotoxicity and IFN-gamma production. However, molecular-mechanism of NK cell activation via NKR-P1 is not well elucidated. In this study, we analyzed the cell surface complex associated with NKR-P1 on NK cells and found that NKR-P1 associates with the FcR gamma chain which is an essential component of Fc receptors for IgG and IgE. The association between FcR gamma and NKR-P1 is independent of Fc receptor complexes. Furthermore, NK cells from FcR gamma-deficient mice did not show cytotoxicity or IFN-gamma production upon NKR-P1 cross-linking. Similarly, NK1.1(+) T cells from FcR gamma-deficient mice did not produce IFN-gamma upon NKR-P1 crosslinking. These findings demonstrate that the FcR gamma chain plays an important role in activation of NK cells via the NKR-P1 molecule.
引用
收藏
页码:1957 / 1963
页数:7
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