TY - JOUR
T1 - NK cell activation through the NKG2D ligand MULT-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene m145
AU - Krmpotic, Astrid
AU - Hasan, Milena
AU - Loewendorf, Andrea
AU - Saulig, Tanja
AU - Halenius, Anne
AU - Lenac, Tihana
AU - Polic, Bojan
AU - Bubic, Ivan
AU - Kriegeskorte, Anja
AU - Pernjak-Pugel, Ester
AU - Messerle, Martin
AU - Hengel, Hartmut
AU - Busch, Dirk H.
AU - Koszinowski, Ulrich H.
AU - Jonjic, Stipan
PY - 2005/1/17
Y1 - 2005/1/17
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=19944432847&partnerID=8YFLogxK
U2 - 10.1084/jem.20041617
DO - 10.1084/jem.20041617
M3 - Article
C2 - 15642742
AN - SCOPUS:19944432847
SN - 0022-1007
VL - 201
SP - 211
EP - 220
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 2
ER -