Differential Susceptibility of RAE-1 Isoforms to Mouse Cytomegalovirus

作者：Arapovic Jurica; Lenac Tihana; Antulov Ronald; Polic Bojan; Ruzsics Zsolt; Carayannopoulos Leonidas N; Koszinowski Ulrich H; Krmpotic Astrid; Jonjic Stipan^*

来源：Journal of Virology, 2009, 83(16): 8198-8207.

DOI：10.1128/JVI.02549-08

The NKG2D receptor is one of the most potent activating natural killer cell receptors involved in antiviral responses. The mouse NKG2D ligands MULT-1, RAE-1, and H60 are regulated by murine cytomegalovirus (MCMV) proteins m145, m152, and m155, respectively. In addition, the m138 protein interferes with the expression of both MULT-1 and H60. We show here that one of five RAE-1 isoforms, RAE-1 delta, is resistant to downregulation by MCMV and that this escape has functional importance in vivo. Although m152 retained newly synthesized RAE-1 delta and RAE-1 gamma in the endoplasmic reticulum, no viral regulator was able to affect the mature RAE-1 delta form which remains expressed on the surfaces of infected cells. This differential susceptibility to downregulation by MCMV is not a consequence of faster maturation of RAE-1 delta compared to RAE-1 gamma but rather an intrinsic property of the mature surface-resident protein. This difference can be attributed to the absence of a PLWY motif from RAE-1 delta. Altogether, these findings provide evidence for a novel mechanism of host escape from viral immunoevasion of NKG2D-dependent control.

• 出版日期2009-8-15