The novel inhibitory NKR-P1C receptor and ly49s3 identify two complementary, functionally distinct NK cell subsets in rats

被引:34
作者
Kveberg, Lise
Back, Camilla J.
Dai, Ke-Zheng
Inngjerdingen, Marit
Rolstad, Bent
Ryan, James C.
Vaage, John T. [1 ]
Naper, Christian
机构
[1] Univ Hosp, Rikshosp, Inst Immunol, NO-0027 Oslo, Norway
[2] Univ Oslo, Inst Basic Med Sci, Dept Anat, N-0316 Oslo, Norway
[3] No Calif Inst Res & Educ, Vet Affairs Med Ctr, San Francisco, CA 94121 USA
[4] Univ Calif San Francisco, San Francisco, CA 94121 USA
关键词
D O I
10.4049/jimmunol.176.7.4133
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The proximal region of the NK gene complex encodes the NKR-P1 family of killer cell lectin-like receptors which in mice bind members of the genetically linked C-type lectin-related family, while the distal region encodes Ly49 receptors for polymorphic MHC class I molecules. Although certain members of the NKR-P1 family are expressed by all NK cells, we have identified a novel inhibitory rat NKR-P1 molecule termed NKR-P1C that is selectively expressed by a Ly49-negative NK subset with unique functional characteristics. NKR-P1C(+) NK cells efficiently lyse certain tumor target cells, secrete cytokines upon stimulation, and functionally recognize a nonpolymorphic ligand on Con A-activated lymphoblasts. However, they specifically fail to kill MHC-mismatched lymphoblast target cells. The NKR-P1C(+) NK cell subset also appears earlier during development and shows a tissue distribution distinct from its complementary Ly49s3(+) subset, which expresses a wide range of Ly49 receptors. These data suggest the existence of two major, functionally distinct populations of rat NK cells possessing very different killer cell lectin-like receptor repertoires.
引用
收藏
页码:4133 / 4140
页数:8
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