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

131 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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