NK cell activation through the NKG2D ligand MULT-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene m145

被引:116
作者
Krmpotic, A
Hasan, M
Loewendorf, A
Saulig, T
Halenius, A
Lenac, T
Polic, B
Bubic, I
Kriegeskorte, A
Pernjak-Pugel, E
Messerle, M
Hengel, H
Busch, DH
Koszinowski, UH
Jonjic, S [1 ]
机构
[1] Univ Rijeka, Fac Med, Dept Histol & Embryol, Rijeka 51000, Croatia
[2] Univ Halle Wittenberg, Fac Med, ZAMED, Virus Cell Interact Grp, D-06120 Halle Saale, Germany
[3] Robert Koch Inst, Div Viral Infect, D-13353 Berlin, Germany
[4] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-90336 Munich, Germany
[5] Univ Munich, Max Von Pettenkofer Inst, D-80336 Munich, Germany
关键词
D O I
10.1084/jem.20041617
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 NK cell-activating receptor NKG2D interacts with three different cellular ligands, all of which are regulated by mouse cytomegalovirus (MCMV). We set out to define the viral gene product regulating murine UL16-binding protein-like transcript (MULT)-1, a newly described NKG2D ligand. We show that MCMV infection strongly induces MULT-1 gene expression, but surface expression of this glycoprotein is nevertheless completely abolished by the virus. Screening a panel of MCMV deletion mutants defined the gene m 145 as the viral regulator of MULT-1. The MCMV m145-encoded glycoprotein turned out to be necessary and sufficient to regulate MULT-1 by preventing plasma membrane residence of MULT-1. The importance of MULT-1 in NK cell regulation in vivo was confirmed by the attenuating effect of the m145 deletion that was lifted after NK cell depletion. Our findings underline the significance of escaping MULT-1/NKG2D signaling for viral survival and maintenance.
引用
收藏
页码:211 / 220
页数:10
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