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Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors

The interferon (IFN) response is a powerful system that was evolutionarily acquired by vertebrates including mammals to protect against viral infection. The cytoplasmic RNA helicases, RIG-I-like receptors (RLRs), were discovered in 2004 as viral sensors that trigger the antiviral IFN response by rec...

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Detalles Bibliográficos
Autores principales: Kato, Hiroki, Fujita, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151769/
http://dx.doi.org/10.1016/B978-0-12-374279-7.02005-1
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author Kato, Hiroki
Fujita, Takashi
author_facet Kato, Hiroki
Fujita, Takashi
author_sort Kato, Hiroki
collection PubMed
description The interferon (IFN) response is a powerful system that was evolutionarily acquired by vertebrates including mammals to protect against viral infection. The cytoplasmic RNA helicases, RIG-I-like receptors (RLRs), were discovered in 2004 as viral sensors that trigger the antiviral IFN response by recognizing the nonself signatures of viral RNAs. The mechanisms underlying the recognition of viral RNAs and signal transduction leading to the production of type I IFN have been intensively studied following the discovery of RLRs. Moreover, a dysregulation in the expression of RLR or aberrant RLR signaling has been implicated in the development of a number of autoimmune diseases. We herein provide an overview of recent advances in RLR research and discussed future directions.
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spelling pubmed-71517692020-04-13 Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors Kato, Hiroki Fujita, Takashi Encyclopedia of Immunobiology Article The interferon (IFN) response is a powerful system that was evolutionarily acquired by vertebrates including mammals to protect against viral infection. The cytoplasmic RNA helicases, RIG-I-like receptors (RLRs), were discovered in 2004 as viral sensors that trigger the antiviral IFN response by recognizing the nonself signatures of viral RNAs. The mechanisms underlying the recognition of viral RNAs and signal transduction leading to the production of type I IFN have been intensively studied following the discovery of RLRs. Moreover, a dysregulation in the expression of RLR or aberrant RLR signaling has been implicated in the development of a number of autoimmune diseases. We herein provide an overview of recent advances in RLR research and discussed future directions. 2016 2016-05-09 /pmc/articles/PMC7151769/ http://dx.doi.org/10.1016/B978-0-12-374279-7.02005-1 Text en Copyright © 2016 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kato, Hiroki
Fujita, Takashi
Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title_full Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title_fullStr Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title_full_unstemmed Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title_short Cytoplasmic Viral RNA Sensors: RIG-I-Like Receptors
title_sort cytoplasmic viral rna sensors: rig-i-like receptors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151769/
http://dx.doi.org/10.1016/B978-0-12-374279-7.02005-1
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AT fujitatakashi cytoplasmicviralrnasensorsrigilikereceptors