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Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases

Interferons (IFNs) bind to cell surface receptors and activate the expression of interferon-stimulated genes (ISGs) through intracellular signaling cascades. ISGs and their expression products have various biological functions, such as antiviral and immunomodulatory effects, and are essential effect...

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Autores principales: Lang, Rui, Li, Huiting, Luo, Xiaoqin, Liu, Cencen, Zhang, Yiwen, Guo, ShunYu, Xu, Jingyi, Bao, Changshun, Dong, Wei, Yu, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618809/
https://www.ncbi.nlm.nih.gov/pubmed/36325336
http://dx.doi.org/10.3389/fimmu.2022.1008072
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author Lang, Rui
Li, Huiting
Luo, Xiaoqin
Liu, Cencen
Zhang, Yiwen
Guo, ShunYu
Xu, Jingyi
Bao, Changshun
Dong, Wei
Yu, Yang
author_facet Lang, Rui
Li, Huiting
Luo, Xiaoqin
Liu, Cencen
Zhang, Yiwen
Guo, ShunYu
Xu, Jingyi
Bao, Changshun
Dong, Wei
Yu, Yang
author_sort Lang, Rui
collection PubMed
description Interferons (IFNs) bind to cell surface receptors and activate the expression of interferon-stimulated genes (ISGs) through intracellular signaling cascades. ISGs and their expression products have various biological functions, such as antiviral and immunomodulatory effects, and are essential effector molecules for IFN function. ISGs limit the invasion and replication of the virus in a cell-specific and region-specific manner in the central nervous system (CNS). In addition to participating in natural immunity against viral infections, studies have shown that ISGs are essential in the pathogenesis of CNS disorders such as neuroinflammation and neurodegenerative diseases. The aim of this review is to present a macroscopic overview of the characteristics of ISGs that restrict viral neural invasion and the expression of the ISGs underlying viral infection of CNS cells. Furthermore, we elucidate the characteristics of ISGs expression in neurological inflammation, neuropsychiatric disorders such as depression as well as neurodegenerative disorders, including Alzheimer’s disease (AD), Parkinson’s disease (PD), and amyotrophic lateral sclerosis (ALS). Finally, we summarize several ISGs (ISG15, IFIT2, IFITM3) that have been studied more in recent years for their antiviral infection in the CNS and their research progress in neurological diseases.
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spelling pubmed-96188092022-11-01 Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases Lang, Rui Li, Huiting Luo, Xiaoqin Liu, Cencen Zhang, Yiwen Guo, ShunYu Xu, Jingyi Bao, Changshun Dong, Wei Yu, Yang Front Immunol Immunology Interferons (IFNs) bind to cell surface receptors and activate the expression of interferon-stimulated genes (ISGs) through intracellular signaling cascades. ISGs and their expression products have various biological functions, such as antiviral and immunomodulatory effects, and are essential effector molecules for IFN function. ISGs limit the invasion and replication of the virus in a cell-specific and region-specific manner in the central nervous system (CNS). In addition to participating in natural immunity against viral infections, studies have shown that ISGs are essential in the pathogenesis of CNS disorders such as neuroinflammation and neurodegenerative diseases. The aim of this review is to present a macroscopic overview of the characteristics of ISGs that restrict viral neural invasion and the expression of the ISGs underlying viral infection of CNS cells. Furthermore, we elucidate the characteristics of ISGs expression in neurological inflammation, neuropsychiatric disorders such as depression as well as neurodegenerative disorders, including Alzheimer’s disease (AD), Parkinson’s disease (PD), and amyotrophic lateral sclerosis (ALS). Finally, we summarize several ISGs (ISG15, IFIT2, IFITM3) that have been studied more in recent years for their antiviral infection in the CNS and their research progress in neurological diseases. Frontiers Media S.A. 2022-10-17 /pmc/articles/PMC9618809/ /pubmed/36325336 http://dx.doi.org/10.3389/fimmu.2022.1008072 Text en Copyright © 2022 Lang, Li, Luo, Liu, Zhang, Guo, Xu, Bao, Dong and Yu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Lang, Rui
Li, Huiting
Luo, Xiaoqin
Liu, Cencen
Zhang, Yiwen
Guo, ShunYu
Xu, Jingyi
Bao, Changshun
Dong, Wei
Yu, Yang
Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title_full Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title_fullStr Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title_full_unstemmed Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title_short Expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (CNS) and neurological diseases
title_sort expression and mechanisms of interferon-stimulated genes in viral infection of the central nervous system (cns) and neurological diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618809/
https://www.ncbi.nlm.nih.gov/pubmed/36325336
http://dx.doi.org/10.3389/fimmu.2022.1008072
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