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Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) 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 pre...

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Autores principales: Kielczewska, Agnieszka, Pyzik, Michal, Sun, Tianhe, Krmpotic, Astrid, Lodoen, Melissa B., Munks, Michael W., Babic, Marina, Hill, Ann B., Koszinowski, Ulrich H., Jonjic, Stipan, Lanier, Lewis L., Vidal, Silvia M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699136/
https://www.ncbi.nlm.nih.gov/pubmed/19255146
http://dx.doi.org/10.1084/jem.20080954
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author Kielczewska, Agnieszka
Pyzik, Michal
Sun, Tianhe
Krmpotic, Astrid
Lodoen, Melissa B.
Munks, Michael W.
Babic, Marina
Hill, Ann B.
Koszinowski, Ulrich H.
Jonjic, Stipan
Lanier, Lewis L.
Vidal, Silvia M.
author_facet Kielczewska, Agnieszka
Pyzik, Michal
Sun, Tianhe
Krmpotic, Astrid
Lodoen, Melissa B.
Munks, Michael W.
Babic, Marina
Hill, Ann B.
Koszinowski, Ulrich H.
Jonjic, Stipan
Lanier, Lewis L.
Vidal, Silvia M.
author_sort Kielczewska, Agnieszka
collection PubMed
description 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-D(k) and the MCMV m04 protein. Using H2 chimeras between H2-D(b) and -D(k), we demonstrate that the H2-D(k) 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-D(k), 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.
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spelling pubmed-26991362009-09-16 Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response Kielczewska, Agnieszka Pyzik, Michal Sun, Tianhe Krmpotic, Astrid Lodoen, Melissa B. Munks, Michael W. Babic, Marina Hill, Ann B. Koszinowski, Ulrich H. Jonjic, Stipan Lanier, Lewis L. Vidal, Silvia M. J Exp Med Brief Definitive Report 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-D(k) and the MCMV m04 protein. Using H2 chimeras between H2-D(b) and -D(k), we demonstrate that the H2-D(k) 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-D(k), 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. The Rockefeller University Press 2009-03-16 /pmc/articles/PMC2699136/ /pubmed/19255146 http://dx.doi.org/10.1084/jem.20080954 Text en © 2009 Kielczewska et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Brief Definitive Report
Kielczewska, Agnieszka
Pyzik, Michal
Sun, Tianhe
Krmpotic, Astrid
Lodoen, Melissa B.
Munks, Michael W.
Babic, Marina
Hill, Ann B.
Koszinowski, Ulrich H.
Jonjic, Stipan
Lanier, Lewis L.
Vidal, Silvia M.
Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title_full Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title_fullStr Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title_full_unstemmed Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title_short Ly49P recognition of cytomegalovirus-infected cells expressing H2-D(k) and CMV-encoded m04 correlates with the NK cell antiviral response
title_sort ly49p recognition of cytomegalovirus-infected cells expressing h2-d(k) and cmv-encoded m04 correlates with the nk cell antiviral response
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699136/
https://www.ncbi.nlm.nih.gov/pubmed/19255146
http://dx.doi.org/10.1084/jem.20080954
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