Missing self-recognition of Ocil/Cir-b by inhibitory NKR-P1 natural killer cell receptors

被引:171
作者
Carlyle, JR
Jamieson, AM
Gasser, S
Clingan, CS
Arase, H
Raulet, DH
机构
[1] Japan Sci & Technol Corp, PRESTO, Precursory Res Embryon Sci & Technol, Kawaguchi 3320012, Japan
[2] Chiba Univ, Grad Sch Med, Dept Mol Genet, Chiba 2608670, Japan
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Canc Res Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1073/pnas.0308304101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The NKR-P1 family of C-type lectin-like receptors are expressed on natural killer (NK) cells and NKT cells. We report the cloning and characterization of a cognate ligand for the inhibitory mouse NK receptors (NKR)-P1B and NKR-P1D (CD161b/d). The NKR-P1B/D ligand is osteoclast inhibitory lectin (Ocil), also known as Clr-b, a member of a previously cloned group of C-type lectin-related (Clr) proteins linked to the NKR-P1 receptors in the mouse NK gene complex (NKC). Expression of Ocil/Clr-b on mouse tumor cell lines inhibits NK cell-mediated killing. Inhibition is blocked with a new mAb (4A6) specific for Ocil/Clr-b. By using 4A6 mAb, we demonstrate that Ocil/Clr-b is displayed at high levels on nearly all hematopoietic cells, with the exception of erythrocytes, in a pattern that is similar to that of class I MHC molecules. Remarkably, Ocil/Clr-b is frequently down-regulated on mouse tumor cell lines, indicating a role for this receptor-ligand system in a new form of "missing self-recoginition" of tumor cells.
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页码:3527 / 3532
页数:6
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