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The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19)
Understanding the potential association between the poly (ADP-ribose) polymerase member 14 (PARP14) and the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may aid in understanding the host immunopathological response to the virus. PARP14 has an emerging role in viral infections, and th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Newlands Press Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818771/ https://www.ncbi.nlm.nih.gov/pubmed/33467912 http://dx.doi.org/10.4155/fmc-2020-0226 |
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author | Tauber, Amanda L Schweiker, Stephanie S Levonis, Stephan M |
author_facet | Tauber, Amanda L Schweiker, Stephanie S Levonis, Stephan M |
author_sort | Tauber, Amanda L |
collection | PubMed |
description | Understanding the potential association between the poly (ADP-ribose) polymerase member 14 (PARP14) and the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may aid in understanding the host immunopathological response to the virus. PARP14 has an emerging role in viral infections, and this article considers its potential mechanisms for action in either a pro- or anti-viral manner. It is evident that more experimental work is required; however, PARP14 appears vital in controlling the interferon response to the SARS-CoV-2 infection and has potential roles in balancing the proinflammatory cytokines of the cytokine storm. Furthermore, the SARS-CoV-2 macrodomain can prevent the PARP14-mediated antiviral response, suggesting a more complex relationship between PARP14 activity and SARS-CoV-2 infections. |
format | Online Article Text |
id | pubmed-7818771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Newlands Press Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78187712021-01-21 The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) Tauber, Amanda L Schweiker, Stephanie S Levonis, Stephan M Future Med Chem Special Report Understanding the potential association between the poly (ADP-ribose) polymerase member 14 (PARP14) and the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may aid in understanding the host immunopathological response to the virus. PARP14 has an emerging role in viral infections, and this article considers its potential mechanisms for action in either a pro- or anti-viral manner. It is evident that more experimental work is required; however, PARP14 appears vital in controlling the interferon response to the SARS-CoV-2 infection and has potential roles in balancing the proinflammatory cytokines of the cytokine storm. Furthermore, the SARS-CoV-2 macrodomain can prevent the PARP14-mediated antiviral response, suggesting a more complex relationship between PARP14 activity and SARS-CoV-2 infections. Newlands Press Ltd 2021-01-20 2021-01 /pmc/articles/PMC7818771/ /pubmed/33467912 http://dx.doi.org/10.4155/fmc-2020-0226 Text en © 2021 Newlands Press This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Special Report Tauber, Amanda L Schweiker, Stephanie S Levonis, Stephan M The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title | The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title_full | The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title_fullStr | The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title_full_unstemmed | The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title_short | The potential association between PARP14 and the SARS-CoV-2 infection (COVID-19) |
title_sort | potential association between parp14 and the sars-cov-2 infection (covid-19) |
topic | Special Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818771/ https://www.ncbi.nlm.nih.gov/pubmed/33467912 http://dx.doi.org/10.4155/fmc-2020-0226 |
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