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Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier

The blood–brain barrier (BBB) consists of highly specialized cells including brain microvascular endothelial cells, astrocytes, microglia, pericytes, and neurons, which act in concert to restrict the entry of pathogens, immune cells, and soluble molecules into the central nervous system (CNS). If pa...

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Detalles Bibliográficos
Autores principales: Miner, Jonathan J, Diamond, Michael S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715944/
https://www.ncbi.nlm.nih.gov/pubmed/26590675
http://dx.doi.org/10.1016/j.coi.2015.10.008
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author Miner, Jonathan J
Diamond, Michael S
author_facet Miner, Jonathan J
Diamond, Michael S
author_sort Miner, Jonathan J
collection PubMed
description The blood–brain barrier (BBB) consists of highly specialized cells including brain microvascular endothelial cells, astrocytes, microglia, pericytes, and neurons, which act in concert to restrict the entry of pathogens, immune cells, and soluble molecules into the central nervous system (CNS). If pathogens manage to cross the BBB and establish infection within the CNS, the BBB can open in a regulated manner to allow leukocyte transmigration into the CNS so that microbes, infected cells, and debris can be cleared. This review highlights how different inflammatory cytokines or signaling pathways disrupt or enhance BBB integrity in a way that regulates entry of neurotropic viruses into the CNS.
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spelling pubmed-47159442017-02-01 Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier Miner, Jonathan J Diamond, Michael S Curr Opin Immunol Article The blood–brain barrier (BBB) consists of highly specialized cells including brain microvascular endothelial cells, astrocytes, microglia, pericytes, and neurons, which act in concert to restrict the entry of pathogens, immune cells, and soluble molecules into the central nervous system (CNS). If pathogens manage to cross the BBB and establish infection within the CNS, the BBB can open in a regulated manner to allow leukocyte transmigration into the CNS so that microbes, infected cells, and debris can be cleared. This review highlights how different inflammatory cytokines or signaling pathways disrupt or enhance BBB integrity in a way that regulates entry of neurotropic viruses into the CNS. Elsevier Ltd. 2016-02 2015-11-16 /pmc/articles/PMC4715944/ /pubmed/26590675 http://dx.doi.org/10.1016/j.coi.2015.10.008 Text en Copyright © 2015 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Miner, Jonathan J
Diamond, Michael S
Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title_full Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title_fullStr Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title_full_unstemmed Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title_short Mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
title_sort mechanisms of restriction of viral neuroinvasion at the blood–brain barrier
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715944/
https://www.ncbi.nlm.nih.gov/pubmed/26590675
http://dx.doi.org/10.1016/j.coi.2015.10.008
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