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Crosstalk Between Mammalian Antiviral Pathways

As part of their innate immune response against viral infections, mammals activate the expression of type I interferons to prevent viral replication and dissemination. An antiviral RNAi-based response can be also activated in mammals, suggesting that several mechanisms can co-occur in the same cell...

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Autores principales: Watson, Samir F., Knol, Lisanne I., Witteveldt, Jeroen, Macias, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468734/
https://www.ncbi.nlm.nih.gov/pubmed/30909383
http://dx.doi.org/10.3390/ncrna5010029
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author Watson, Samir F.
Knol, Lisanne I.
Witteveldt, Jeroen
Macias, Sara
author_facet Watson, Samir F.
Knol, Lisanne I.
Witteveldt, Jeroen
Macias, Sara
author_sort Watson, Samir F.
collection PubMed
description As part of their innate immune response against viral infections, mammals activate the expression of type I interferons to prevent viral replication and dissemination. An antiviral RNAi-based response can be also activated in mammals, suggesting that several mechanisms can co-occur in the same cell and that these pathways must interact to enable the best antiviral response. Here, we will review how the classical type I interferon response and the recently described antiviral RNAi pathways interact in mammalian cells. Specifically, we will uncover how the small RNA biogenesis pathway, composed by the nucleases Drosha and Dicer can act as direct antiviral factors, and how the type-I interferon response regulates the function of these. We will also describe how the factors involved in small RNA biogenesis and specific small RNAs impact the activation of the type I interferon response and antiviral activity. With this, we aim to expose the complex and intricate network of interactions between the different antiviral pathways in mammals.
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spelling pubmed-64687342019-04-19 Crosstalk Between Mammalian Antiviral Pathways Watson, Samir F. Knol, Lisanne I. Witteveldt, Jeroen Macias, Sara Noncoding RNA Review As part of their innate immune response against viral infections, mammals activate the expression of type I interferons to prevent viral replication and dissemination. An antiviral RNAi-based response can be also activated in mammals, suggesting that several mechanisms can co-occur in the same cell and that these pathways must interact to enable the best antiviral response. Here, we will review how the classical type I interferon response and the recently described antiviral RNAi pathways interact in mammalian cells. Specifically, we will uncover how the small RNA biogenesis pathway, composed by the nucleases Drosha and Dicer can act as direct antiviral factors, and how the type-I interferon response regulates the function of these. We will also describe how the factors involved in small RNA biogenesis and specific small RNAs impact the activation of the type I interferon response and antiviral activity. With this, we aim to expose the complex and intricate network of interactions between the different antiviral pathways in mammals. MDPI 2019-03-22 /pmc/articles/PMC6468734/ /pubmed/30909383 http://dx.doi.org/10.3390/ncrna5010029 Text en © 2019 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
Watson, Samir F.
Knol, Lisanne I.
Witteveldt, Jeroen
Macias, Sara
Crosstalk Between Mammalian Antiviral Pathways
title Crosstalk Between Mammalian Antiviral Pathways
title_full Crosstalk Between Mammalian Antiviral Pathways
title_fullStr Crosstalk Between Mammalian Antiviral Pathways
title_full_unstemmed Crosstalk Between Mammalian Antiviral Pathways
title_short Crosstalk Between Mammalian Antiviral Pathways
title_sort crosstalk between mammalian antiviral pathways
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468734/
https://www.ncbi.nlm.nih.gov/pubmed/30909383
http://dx.doi.org/10.3390/ncrna5010029
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