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MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling

MHC class I molecules are key in the presentation of antigen and initiation of adaptive CD8+ T cell responses. In addition to its classical activity, MHC I may possess nonclassical functions. We have previously identified a regulatory role of MHC I in TLR signaling and antibacterial immunity. Howeve...

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Detalles Bibliográficos
Autores principales: Xia, Simo, Tao, Yijie, Cui, Likun, Yu, Yizhi, Xu, Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754968/
https://www.ncbi.nlm.nih.gov/pubmed/31583257
http://dx.doi.org/10.1155/2019/5370706
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author Xia, Simo
Tao, Yijie
Cui, Likun
Yu, Yizhi
Xu, Sheng
author_facet Xia, Simo
Tao, Yijie
Cui, Likun
Yu, Yizhi
Xu, Sheng
author_sort Xia, Simo
collection PubMed
description MHC class I molecules are key in the presentation of antigen and initiation of adaptive CD8+ T cell responses. In addition to its classical activity, MHC I may possess nonclassical functions. We have previously identified a regulatory role of MHC I in TLR signaling and antibacterial immunity. However, its role in innate antiviral immunity remains unknown. In this study, we found a reduced viral load in MHC I-deficient macrophages that was independent of type I IFN production. Mechanically, MHC I mediated viral suppression by inhibiting the type I IFN signaling pathway, which depends on SHP2. Cross-linking MHC I at the membrane increased SHP2 activation and further suppressed STAT1 phosphorylation. Therefore, our data revealed an inhibitory role of MHC I in type I IFN response to viral infection and expanded our understanding of MHC I and antigen presentation.
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spelling pubmed-67549682019-10-03 MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling Xia, Simo Tao, Yijie Cui, Likun Yu, Yizhi Xu, Sheng J Immunol Res Research Article MHC class I molecules are key in the presentation of antigen and initiation of adaptive CD8+ T cell responses. In addition to its classical activity, MHC I may possess nonclassical functions. We have previously identified a regulatory role of MHC I in TLR signaling and antibacterial immunity. However, its role in innate antiviral immunity remains unknown. In this study, we found a reduced viral load in MHC I-deficient macrophages that was independent of type I IFN production. Mechanically, MHC I mediated viral suppression by inhibiting the type I IFN signaling pathway, which depends on SHP2. Cross-linking MHC I at the membrane increased SHP2 activation and further suppressed STAT1 phosphorylation. Therefore, our data revealed an inhibitory role of MHC I in type I IFN response to viral infection and expanded our understanding of MHC I and antigen presentation. Hindawi 2019-09-09 /pmc/articles/PMC6754968/ /pubmed/31583257 http://dx.doi.org/10.1155/2019/5370706 Text en Copyright © 2019 Simo Xia et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xia, Simo
Tao, Yijie
Cui, Likun
Yu, Yizhi
Xu, Sheng
MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title_full MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title_fullStr MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title_full_unstemmed MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title_short MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling
title_sort mhc class i molecules exacerbate viral infection by disrupting type i interferon signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754968/
https://www.ncbi.nlm.nih.gov/pubmed/31583257
http://dx.doi.org/10.1155/2019/5370706
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