| Literature DB >> 28760883 |
Tsukasa Nabekura1,2,3, Dagmar Gotthardt1,2, Kouta Niizuma1,4, Tihana Trsan5, Tina Jenus5, Stipan Jonjic5, Lewis L Lanier6,2.
Abstract
NK cells play a critical role in host defense against viruses. In this study, we investigated the role of NKG2D in the expansion of NK cells after mouse CMV (MCMV) infection. Wild-type and NKG2D-deficient (Klrk1-/- ) Ly49H+ NK cells proliferated robustly when infected with MCMV strains engineered to allow expression of NKG2D ligands, which enhanced the response of wild-type NK cells. Naive NK cells exclusively express NKG2D-L, which pairs only with DAP10, whereas NKG2D-S expressed by activated NK cells pairs with DAP10 and DAP12, similar to Ly49H. However, NKG2D alone was unable to drive robust expansion of Ly49H- NK cells when mice were infected with these MCMV strains, likely because NKG2D-S was only transiently expressed postinfection. These findings demonstrate that NKG2D augments Ly49H-dependent proliferation of NK cells; however, NKG2D signaling alone is inadequate for expansion of NK cells, likely due to only transient expression of the NKG2D-DAP12 complex.Entities:
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Year: 2017 PMID: 28760883 PMCID: PMC5567695 DOI: 10.4049/jimmunol.1700799
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422