Krmpotic Astrid, Hasan Milena, Loewendorf Andrea, Saulig Tanja, Halenius Anne, Lenac Tihana, Polic Bojan, Bubic Ivan, Kriegeskorte Anja, Pernjak-Pugel Ester, Messerle Martin, Hengel Hartmut, Busch Dirk H, Koszinowski Ulrich H, Jonjic Stipan
Department of Histology and Embryology, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.
J Exp Med. 2005 Jan 17;201(2):211-20. doi: 10.1084/jem.20041617. Epub 2005 Jan 10.
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.
自然杀伤(NK)细胞激活受体NKG2D与三种不同的细胞配体相互作用,所有这些配体均受小鼠巨细胞病毒(MCMV)调控。我们着手确定调节小鼠UL16结合蛋白样转录本(MULT)-1(一种新描述的NKG2D配体)的病毒基因产物。我们发现,MCMV感染强烈诱导MULT-1基因表达,但该病毒却完全消除了这种糖蛋白的表面表达。筛选一组MCMV缺失突变体确定了m145基因是MULT-1的病毒调节因子。结果表明,MCMV m145编码的糖蛋白通过阻止MULT-1在质膜上停留来调节MULT-1,这一作用既必要又充分。m145缺失的减弱效应在NK细胞耗竭后消除,从而证实了MULT-1在体内NK细胞调节中的重要性。我们的研究结果强调了逃避MULT-1/NKG2D信号传导对病毒生存和维持的重要性。