Affiliation:
1. Department of Life Sciences and Chemistry, Jacobs University, Bremen 28759, Germany
2. Department of Medicine Huddinge, Karolinska Institutet, Stockholm 14152, Sweden
Abstract
ABSTRACT
NKG2D (also known as KLRK1) is a crucial natural killer (NK) cell-activating receptor, and the murine cytomegalovirus (MCMV) employs multiple immunoevasins to avoid NKG2D-mediated activation. One of the MCMV immunoevasins, gp40 (m152), downregulates the cell surface NKG2D ligand RAE-1γ (also known as Raet1c) thus limiting NK cell activation. This study establishes the molecular mechanism by which gp40 retains RAE-1γ in the secretory pathway. Using flow cytometry and pulse-chase analysis, we demonstrate that gp40 retains RAE-1γ in the early secretory pathway, and that this effect depends on the binding of gp40 to a host protein, TMED10, a member of the p24 protein family. We also show that the TMED10-based retention mechanism can be saturated, and that gp40 has a backup mechanism as it masks RAE-1γ on the cell surface, blocking the interaction with the NKG2D receptor and thus NK cell activation.
Funder
Deutsche Forschungsgemeinschaft
Tönjes Vagt Foundation of Bremen
Publisher
The Company of Biologists
Cited by
6 articles.
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