Recognition of a virus-encoded ligand by a natural killer cell activation receptor

被引:605
作者
Smith, HRC
Heusel, JW
Mehta, IK
Kim, S
Dorner, BG
Naidenko, OV
Iizuka, K
Furukawa, H
Beckman, DL
Pingel, JT
Scalzo, AA
Fremont, DH
Yokoyama, WM
机构
[1] Washington Univ, Sch Med, Howard Hughes Med Inst, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Rheumatol, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[4] Barnes Jewish Hosp, St Louis, MO 63110 USA
[5] Univ Western Australia, Queen Elizabeth II Med Ctr, Dept Microbiol, Nedlands, WA 6907, Australia
关键词
D O I
10.1073/pnas.092258599
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
Natural killer (NK) cells express inhibitory and activation receptors that recognize MHC class I-like molecules on target cells. These receptors may be involved in the critical role of NK cells in controlling initial phases of certain viral infections. indeed, the Ly49H NK cell activation receptor confers in vivo genetic resistance to murine cytomegalovirus (MCMV) infections, but its ligand was previously unknown. Herein, we use heterologous reporter cells to demonstrate that Ly49H recognizes MCMV-infected cells and a ligand encoded by MCMV itself. Exploiting a bioinformatics approach to the MCMV genome, we find at least 11 ORFs for molecules with previously unrecognized features of predicted MHC-like folds and limited MHC sequence homology. We identify one of these, m157, as the ligand for Ly49H. m157 triggers Ly49H-mediated cytotoxicity, and cytokine and chemokine production by freshly isolated INK cells. We hypothesize that the other ORF's with predicted MHC-like folds may be involved in immune evasion or interactions with other NK cell receptors.
引用
收藏
页码:8826 / 8831
页数:6
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