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

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

Research output: Contribution to journalArticlepeer-review

130 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)211-220
Number of pages10
JournalJournal of Experimental Medicine
Volume201
Issue number2
DOIs
StatePublished - 17 Jan 2005

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