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Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus

Multicellular organisms have evolved multiple genetically programmed cell death pathways that are essential for homeostasis. The finding that many viruses encode cell death inhibitors suggested that cellular suicide also functions as a first line of defence against invading pathogens. This theory wa...

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Autores principales: Brune, Wolfram, Andoniou, Christopher E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618015/
https://www.ncbi.nlm.nih.gov/pubmed/28869497
http://dx.doi.org/10.3390/v9090249
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author Brune, Wolfram
Andoniou, Christopher E.
author_facet Brune, Wolfram
Andoniou, Christopher E.
author_sort Brune, Wolfram
collection PubMed
description Multicellular organisms have evolved multiple genetically programmed cell death pathways that are essential for homeostasis. The finding that many viruses encode cell death inhibitors suggested that cellular suicide also functions as a first line of defence against invading pathogens. This theory was confirmed by studying viral mutants that lack certain cell death inhibitors. Cytomegaloviruses, a family of species-specific viruses, have proved particularly useful in this respect. Cytomegaloviruses are known to encode multiple death inhibitors that are required for efficient viral replication. Here, we outline the mechanisms used by the host cell to detect cytomegalovirus infection and discuss the methods employed by the cytomegalovirus family to prevent death of the host cell. In addition to enhancing our understanding of cytomegalovirus pathogenesis we detail how this research has provided significant insights into the cross-talk that exists between the various cell death pathways.
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spelling pubmed-56180152017-09-29 Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus Brune, Wolfram Andoniou, Christopher E. Viruses Review Multicellular organisms have evolved multiple genetically programmed cell death pathways that are essential for homeostasis. The finding that many viruses encode cell death inhibitors suggested that cellular suicide also functions as a first line of defence against invading pathogens. This theory was confirmed by studying viral mutants that lack certain cell death inhibitors. Cytomegaloviruses, a family of species-specific viruses, have proved particularly useful in this respect. Cytomegaloviruses are known to encode multiple death inhibitors that are required for efficient viral replication. Here, we outline the mechanisms used by the host cell to detect cytomegalovirus infection and discuss the methods employed by the cytomegalovirus family to prevent death of the host cell. In addition to enhancing our understanding of cytomegalovirus pathogenesis we detail how this research has provided significant insights into the cross-talk that exists between the various cell death pathways. MDPI 2017-09-02 /pmc/articles/PMC5618015/ /pubmed/28869497 http://dx.doi.org/10.3390/v9090249 Text en © 2017 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
Brune, Wolfram
Andoniou, Christopher E.
Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title_full Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title_fullStr Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title_full_unstemmed Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title_short Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
title_sort die another day: inhibition of cell death pathways by cytomegalovirus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618015/
https://www.ncbi.nlm.nih.gov/pubmed/28869497
http://dx.doi.org/10.3390/v9090249
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