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Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation

Interferons (IFNs) are a group of secreted proteins that play critical roles in antiviral immunity, antitumor activity, activation of cytotoxic T cells, and modulation of host immune responses. IFNs are cytokines, and bind receptors on cell surfaces to trigger signal transduction. The major signalin...

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Detalles Bibliográficos
Autores principales: Nan, Yuchen, Wu, Chunyan, Zhang, Yan-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923490/
https://www.ncbi.nlm.nih.gov/pubmed/29662014
http://dx.doi.org/10.3390/v10040196
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author Nan, Yuchen
Wu, Chunyan
Zhang, Yan-Jin
author_facet Nan, Yuchen
Wu, Chunyan
Zhang, Yan-Jin
author_sort Nan, Yuchen
collection PubMed
description Interferons (IFNs) are a group of secreted proteins that play critical roles in antiviral immunity, antitumor activity, activation of cytotoxic T cells, and modulation of host immune responses. IFNs are cytokines, and bind receptors on cell surfaces to trigger signal transduction. The major signaling pathway activated by IFNs is the JAK/STAT (Janus kinase/signal transducer and activator of transcription) pathway, a complex pathway involved in both viral and host survival strategies. On the one hand, viruses have evolved strategies to escape from antiviral host defenses evoked by IFN-activated JAK/STAT signaling. On the other hand, viruses have also evolved to exploit the JAK/STAT pathway to evoke activation of certain STATs that somehow promote viral pathogenesis. In this review, recent progress in our understanding of the virus-induced IFN-independent STAT signaling and its potential roles in viral induced inflammation and pathogenesis are summarized in detail, and perspectives are provided.
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spelling pubmed-59234902018-05-03 Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation Nan, Yuchen Wu, Chunyan Zhang, Yan-Jin Viruses Review Interferons (IFNs) are a group of secreted proteins that play critical roles in antiviral immunity, antitumor activity, activation of cytotoxic T cells, and modulation of host immune responses. IFNs are cytokines, and bind receptors on cell surfaces to trigger signal transduction. The major signaling pathway activated by IFNs is the JAK/STAT (Janus kinase/signal transducer and activator of transcription) pathway, a complex pathway involved in both viral and host survival strategies. On the one hand, viruses have evolved strategies to escape from antiviral host defenses evoked by IFN-activated JAK/STAT signaling. On the other hand, viruses have also evolved to exploit the JAK/STAT pathway to evoke activation of certain STATs that somehow promote viral pathogenesis. In this review, recent progress in our understanding of the virus-induced IFN-independent STAT signaling and its potential roles in viral induced inflammation and pathogenesis are summarized in detail, and perspectives are provided. MDPI 2018-04-14 /pmc/articles/PMC5923490/ /pubmed/29662014 http://dx.doi.org/10.3390/v10040196 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nan, Yuchen
Wu, Chunyan
Zhang, Yan-Jin
Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title_full Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title_fullStr Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title_full_unstemmed Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title_short Interferon Independent Non-Canonical STAT Activation and Virus Induced Inflammation
title_sort interferon independent non-canonical stat activation and virus induced inflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923490/
https://www.ncbi.nlm.nih.gov/pubmed/29662014
http://dx.doi.org/10.3390/v10040196
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