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Viral Suppression of RIPK1-Mediated Signaling

Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) has emerged as a key upstream regulator of cell death and inflammation. RIPK1-mediated signaling governs the outcome of signaling pathways initiated by tumor necrosis factor receptor 1 (TNFR1), Toll-like receptor 3 (TLR3), TLR4, retinoic...

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Detalles Bibliográficos
Autores principales: Udawatte, Darshika J., Rothman, Alan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406217/
https://www.ncbi.nlm.nih.gov/pubmed/34372694
http://dx.doi.org/10.1128/mBio.01723-21
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author Udawatte, Darshika J.
Rothman, Alan L.
author_facet Udawatte, Darshika J.
Rothman, Alan L.
author_sort Udawatte, Darshika J.
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description Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) has emerged as a key upstream regulator of cell death and inflammation. RIPK1-mediated signaling governs the outcome of signaling pathways initiated by tumor necrosis factor receptor 1 (TNFR1), Toll-like receptor 3 (TLR3), TLR4, retinoic acid-inducible gene 1 (RIG-I)/melanoma differentiation-associated protein 5 (MDA-5), and Z-binding protein 1 (ZBP1) by signaling for NF-κB activation, mitogen-associated protein kinase (MAPK) and interferon regulatory factor 3/7 (IRF3/7) phosphorylation, and cell death via apoptosis and necroptosis. Both cell death and inflammatory responses play a major role in controlling virus infections. Therefore, viruses have evolved multifaceted mechanisms to exploit host immune responses by targeting RIPK1. This review focuses on the current understanding of RIPK1-mediated inflammatory and cell death pathways and multiple mechanisms by which viruses manipulate these pathways by targeting RIPK1. We also discuss gaps in our knowledge regarding RIPK1-mediated signaling pathways and highlight potential avenues for future research.
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spelling pubmed-84062172021-09-09 Viral Suppression of RIPK1-Mediated Signaling Udawatte, Darshika J. Rothman, Alan L. mBio Minireview Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) has emerged as a key upstream regulator of cell death and inflammation. RIPK1-mediated signaling governs the outcome of signaling pathways initiated by tumor necrosis factor receptor 1 (TNFR1), Toll-like receptor 3 (TLR3), TLR4, retinoic acid-inducible gene 1 (RIG-I)/melanoma differentiation-associated protein 5 (MDA-5), and Z-binding protein 1 (ZBP1) by signaling for NF-κB activation, mitogen-associated protein kinase (MAPK) and interferon regulatory factor 3/7 (IRF3/7) phosphorylation, and cell death via apoptosis and necroptosis. Both cell death and inflammatory responses play a major role in controlling virus infections. Therefore, viruses have evolved multifaceted mechanisms to exploit host immune responses by targeting RIPK1. This review focuses on the current understanding of RIPK1-mediated inflammatory and cell death pathways and multiple mechanisms by which viruses manipulate these pathways by targeting RIPK1. We also discuss gaps in our knowledge regarding RIPK1-mediated signaling pathways and highlight potential avenues for future research. American Society for Microbiology 2021-08-10 /pmc/articles/PMC8406217/ /pubmed/34372694 http://dx.doi.org/10.1128/mBio.01723-21 Text en Copyright © 2021 Udawatte and Rothman. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Minireview
Udawatte, Darshika J.
Rothman, Alan L.
Viral Suppression of RIPK1-Mediated Signaling
title Viral Suppression of RIPK1-Mediated Signaling
title_full Viral Suppression of RIPK1-Mediated Signaling
title_fullStr Viral Suppression of RIPK1-Mediated Signaling
title_full_unstemmed Viral Suppression of RIPK1-Mediated Signaling
title_short Viral Suppression of RIPK1-Mediated Signaling
title_sort viral suppression of ripk1-mediated signaling
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406217/
https://www.ncbi.nlm.nih.gov/pubmed/34372694
http://dx.doi.org/10.1128/mBio.01723-21
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