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 m145 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.
NK cell activation through the NKG2D ligand MULT-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene m145
Abbreviations used: HCMV, human CMV; MCMV, mouse CMV; MEF, mouse embryonic fibroblast; MOI, multiplicity of infection; MULT, murine UL16-binding protein-like transcript; ORF, open reading frame; RAE, retinoic acid early inducible.
H. Hengel's present address is Institute for Virology, Heinrich Heine University Duesseldorf, 40225 Duesseldorf, Germany.
The online version of this article contains supplemental material.
Astrid Krmpotic, Milena Hasan, Andrea Loewendorf, Tanja Saulig, Anne Halenius, Tihana Lenac, Bojan Polic, Ivan Bubic, Anja Kriegeskorte, Ester Pernjak-Pugel, Martin Messerle, Hartmut Hengel, Dirk H. Busch, Ulrich H. Koszinowski, Stipan Jonjic; NK cell activation through the NKG2D ligand MULT-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene m145 . J Exp Med 17 January 2005; 201 (2): 211–220. doi: https://doi.org/10.1084/jem.20041617
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