Ly49P recognition of cytomegalovirus-infected cells expressing H2-Dk and CMV-encoded m04 correlates with the NK cell antiviral response
Ly49P recognition of cytomegalovirus-infected cells expressing H2-Dk and CMV-encoded m04 correlates with the NK cell antiviral response
Natural killer (NK) cells are crucial in resistance to certain viral infections, but the mechanisms used to recognize infected cells remain largely unknown. Here, we show that the activating Ly49P receptor recognizes cells infected with mouse cytomegalovirus (MCMV) by a process that requires the presence of H2-Dk and the MCMV m04 protein. Using H2 chimeras between H2-Db and -Dk, we demonstrate that the H2-Dk peptide-binding platform is required for Ly49P recognition. We identified m04 as a viral component necessary for recognition using a panel of MCMV-deletion mutant viruses and complementation of m04-deletion mutant (Δm04) virus infection. MA/My mice, which express Ly49P and H2-Dk, are resistant to MCMV; however, infection with Δm04 MCMV abrogates resistance. Depletion of NK cells in MA/My mice abrogates their resistance to wild-type MCMV infection, but does not significantly affect viral titers in mice infected with Δm04 virus, implicating NK cells in host protection through m04-dependent recognition. These findings reveal a novel mechanism of major histocompatability complex class I–restricted recognition of virally infected cells by an activating NK cell receptor.
- Ludwig-Maximilians-Universität München Germany
- Department of Human Genetics Switzerland
- Oregon Health & Science University United States
- UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
- University of California System United States
Protein Structure, Muromegalovirus, Immunology, 610, NK cells, Lymphocyte Activation, Medical and Health Sciences, Antiviral Agents, Vaccine Related, antiviral response, Mice, Viral Proteins, Immunologic, Biodefense, Receptors, antiviral response; CMV; NK cells, 2.1 Biological and endogenous factors, Killer Cells, Animals, Aetiology, Receptors, Immunologic, Glycoproteins, Prevention, Histocompatibility Antigens Class I, CMV, Brief Definitive Report, Herpesviridae Infections, Protein Structure, Tertiary, Killer Cells, Natural, Emerging Infectious Diseases, Infectious Diseases, Mutation, Natural, NIH 3T3 Cells, Biological Assay, Infection, Carrier Proteins, Tertiary
Protein Structure, Muromegalovirus, Immunology, 610, NK cells, Lymphocyte Activation, Medical and Health Sciences, Antiviral Agents, Vaccine Related, antiviral response, Mice, Viral Proteins, Immunologic, Biodefense, Receptors, antiviral response; CMV; NK cells, 2.1 Biological and endogenous factors, Killer Cells, Animals, Aetiology, Receptors, Immunologic, Glycoproteins, Prevention, Histocompatibility Antigens Class I, CMV, Brief Definitive Report, Herpesviridae Infections, Protein Structure, Tertiary, Killer Cells, Natural, Emerging Infectious Diseases, Infectious Diseases, Mutation, Natural, NIH 3T3 Cells, Biological Assay, Infection, Carrier Proteins, Tertiary
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