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Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation

Despite the crucial role of innate immunity in preventing or controlling pathogen-induced damage in most, if not all, cell types, very little is known about the activity of this essential defense system in central nervous system neurons, especially in humans. In this report we use both an establishe...

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Autores principales: Farmer, Jocelyn R., Altschaefl, Kate M., O'Shea, K. Sue, Miller, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591356/
https://www.ncbi.nlm.nih.gov/pubmed/23505563
http://dx.doi.org/10.1371/journal.pone.0058813
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author Farmer, Jocelyn R.
Altschaefl, Kate M.
O'Shea, K. Sue
Miller, David J.
author_facet Farmer, Jocelyn R.
Altschaefl, Kate M.
O'Shea, K. Sue
Miller, David J.
author_sort Farmer, Jocelyn R.
collection PubMed
description Despite the crucial role of innate immunity in preventing or controlling pathogen-induced damage in most, if not all, cell types, very little is known about the activity of this essential defense system in central nervous system neurons, especially in humans. In this report we use both an established neuronal cell line model and an embryonic stem cell-based system to examine human neuronal innate immunity and responses to neurotropic alphavirus infection in cultured cells. We demonstrate that neuronal differentiation is associated with increased expression of crucial type I interferon signaling pathway components, including interferon regulatory factor-9 and an interferon receptor heterodimer subunit, which results in enhanced interferon stimulation and subsequent heightened antiviral activity and cytoprotective responses against neurotropic alphaviruses such as western equine encephalitis virus. These results identify important differentiation-dependent changes in innate immune system function that control cell-autonomous neuronal responses. Furthermore, this work demonstrates the utility of human embryonic stem cell-derived cultures as a platform to study the interactions between innate immunity, virus infection, and pathogenesis in central nervous system neurons.
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spelling pubmed-35913562013-03-15 Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation Farmer, Jocelyn R. Altschaefl, Kate M. O'Shea, K. Sue Miller, David J. PLoS One Research Article Despite the crucial role of innate immunity in preventing or controlling pathogen-induced damage in most, if not all, cell types, very little is known about the activity of this essential defense system in central nervous system neurons, especially in humans. In this report we use both an established neuronal cell line model and an embryonic stem cell-based system to examine human neuronal innate immunity and responses to neurotropic alphavirus infection in cultured cells. We demonstrate that neuronal differentiation is associated with increased expression of crucial type I interferon signaling pathway components, including interferon regulatory factor-9 and an interferon receptor heterodimer subunit, which results in enhanced interferon stimulation and subsequent heightened antiviral activity and cytoprotective responses against neurotropic alphaviruses such as western equine encephalitis virus. These results identify important differentiation-dependent changes in innate immune system function that control cell-autonomous neuronal responses. Furthermore, this work demonstrates the utility of human embryonic stem cell-derived cultures as a platform to study the interactions between innate immunity, virus infection, and pathogenesis in central nervous system neurons. Public Library of Science 2013-03-07 /pmc/articles/PMC3591356/ /pubmed/23505563 http://dx.doi.org/10.1371/journal.pone.0058813 Text en © 2013 Farmer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Farmer, Jocelyn R.
Altschaefl, Kate M.
O'Shea, K. Sue
Miller, David J.
Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title_full Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title_fullStr Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title_full_unstemmed Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title_short Activation of the Type I Interferon Pathway Is Enhanced in Response to Human Neuronal Differentiation
title_sort activation of the type i interferon pathway is enhanced in response to human neuronal differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591356/
https://www.ncbi.nlm.nih.gov/pubmed/23505563
http://dx.doi.org/10.1371/journal.pone.0058813
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