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Beclin-1 Targeting for Viral Immune Escape

Macroautophagy is a catabolic pathway in eukaryotic cells that has recently been shown to facilitate pathogen detection, pathogen restriction and pathogen-derived antigen presentation to CD4(+) T cells. Due to these protective functions during immune responses, several pathogens, including RNA and D...

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Detalles Bibliográficos
Autor principal: Münz, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185790/
https://www.ncbi.nlm.nih.gov/pubmed/21994775
http://dx.doi.org/10.3390/v3071166
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author Münz, Christian
author_facet Münz, Christian
author_sort Münz, Christian
collection PubMed
description Macroautophagy is a catabolic pathway in eukaryotic cells that has recently been shown to facilitate pathogen detection, pathogen restriction and pathogen-derived antigen presentation to CD4(+) T cells. Due to these protective functions during immune responses, several pathogens, including RNA and DNA viruses, have developed strategies to inhibit autophagosome generation or maturation. Interestingly, most of the respective viral proteins exert these functions via binding to Beclin-1, an essential macroautophagy protein that constitutes part of the phosphatidylinositol-3 kinase complexes that mark membranes for autophagosome generation and facilitate autophagosome fusion with lyososomes. The viruses that inhibit macroautophagy by this pathway include herpesviruses, HIV and influenza A virus. Inhibition either before or after autophagosome formation seems to benefit their viral replication by different mechanisms, which are discussed here.
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spelling pubmed-31857902011-10-12 Beclin-1 Targeting for Viral Immune Escape Münz, Christian Viruses Review Macroautophagy is a catabolic pathway in eukaryotic cells that has recently been shown to facilitate pathogen detection, pathogen restriction and pathogen-derived antigen presentation to CD4(+) T cells. Due to these protective functions during immune responses, several pathogens, including RNA and DNA viruses, have developed strategies to inhibit autophagosome generation or maturation. Interestingly, most of the respective viral proteins exert these functions via binding to Beclin-1, an essential macroautophagy protein that constitutes part of the phosphatidylinositol-3 kinase complexes that mark membranes for autophagosome generation and facilitate autophagosome fusion with lyososomes. The viruses that inhibit macroautophagy by this pathway include herpesviruses, HIV and influenza A virus. Inhibition either before or after autophagosome formation seems to benefit their viral replication by different mechanisms, which are discussed here. Molecular Diversity Preservation International (MDPI) 2011-07-12 /pmc/articles/PMC3185790/ /pubmed/21994775 http://dx.doi.org/10.3390/v3071166 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Münz, Christian
Beclin-1 Targeting for Viral Immune Escape
title Beclin-1 Targeting for Viral Immune Escape
title_full Beclin-1 Targeting for Viral Immune Escape
title_fullStr Beclin-1 Targeting for Viral Immune Escape
title_full_unstemmed Beclin-1 Targeting for Viral Immune Escape
title_short Beclin-1 Targeting for Viral Immune Escape
title_sort beclin-1 targeting for viral immune escape
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185790/
https://www.ncbi.nlm.nih.gov/pubmed/21994775
http://dx.doi.org/10.3390/v3071166
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