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New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells

The nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) family of transcription factors is a key component of the host innate immune response to infectious adenoviruses and adenovirus vectors. In this review, we will discuss a regulatory adenoviral protein encoded by early region 3...

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Autor principal: Carlin, Cathleen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723309/
https://www.ncbi.nlm.nih.gov/pubmed/31349602
http://dx.doi.org/10.3390/microorganisms7080216
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author Carlin, Cathleen R.
author_facet Carlin, Cathleen R.
author_sort Carlin, Cathleen R.
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description The nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) family of transcription factors is a key component of the host innate immune response to infectious adenoviruses and adenovirus vectors. In this review, we will discuss a regulatory adenoviral protein encoded by early region 3 (E3) called E3-RIDα, which targets NFκB through subversion of novel host cell pathways. E3-RIDα down-regulates an EGF receptor signaling pathway, which overrides NFκB negative feedback control in the nucleus, and is induced by cell stress associated with viral infection and exposure to the pro-inflammatory cytokine TNF-α. E3-RIDα also modulates NFκB signaling downstream of the lipopolysaccharide receptor, Toll-like receptor 4, through formation of membrane contact sites controlling cholesterol levels in endosomes. These innate immune evasion tactics have yielded unique perspectives regarding the potential physiological functions of host cell pathways with important roles in infectious disease.
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spelling pubmed-67233092019-09-10 New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells Carlin, Cathleen R. Microorganisms Review The nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) family of transcription factors is a key component of the host innate immune response to infectious adenoviruses and adenovirus vectors. In this review, we will discuss a regulatory adenoviral protein encoded by early region 3 (E3) called E3-RIDα, which targets NFκB through subversion of novel host cell pathways. E3-RIDα down-regulates an EGF receptor signaling pathway, which overrides NFκB negative feedback control in the nucleus, and is induced by cell stress associated with viral infection and exposure to the pro-inflammatory cytokine TNF-α. E3-RIDα also modulates NFκB signaling downstream of the lipopolysaccharide receptor, Toll-like receptor 4, through formation of membrane contact sites controlling cholesterol levels in endosomes. These innate immune evasion tactics have yielded unique perspectives regarding the potential physiological functions of host cell pathways with important roles in infectious disease. MDPI 2019-07-25 /pmc/articles/PMC6723309/ /pubmed/31349602 http://dx.doi.org/10.3390/microorganisms7080216 Text en © 2019 by the author. 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
Carlin, Cathleen R.
New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title_full New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title_fullStr New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title_full_unstemmed New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title_short New Insights to Adenovirus-Directed Innate Immunity in Respiratory Epithelial Cells
title_sort new insights to adenovirus-directed innate immunity in respiratory epithelial cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6723309/
https://www.ncbi.nlm.nih.gov/pubmed/31349602
http://dx.doi.org/10.3390/microorganisms7080216
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