Cargando…

Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells

Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells. Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated...

Descripción completa

Detalles Bibliográficos
Autores principales: Miura, Tanya A, Holmes, Kathryn V
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774885/
https://www.ncbi.nlm.nih.gov/pubmed/19638499
http://dx.doi.org/10.1189/jlb.0209078
_version_ 1782173977502810112
author Miura, Tanya A
Holmes, Kathryn V
author_facet Miura, Tanya A
Holmes, Kathryn V
author_sort Miura, Tanya A
collection PubMed
description Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells. Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune-mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung.
format Text
id pubmed-2774885
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-27748852010-11-01 Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells Miura, Tanya A Holmes, Kathryn V J Leukoc Biol Mini-Reviews Innate immune responses in coronavirus infections of the respiratory tract are analyzed in primary differentiated airway and alveolar epithelial cells. Viruses that infect the lung are a significant cause of morbidity and mortality in animals and humans worldwide. Coronaviruses are being associated increasingly with severe diseases in the lower respiratory tract. Alveolar epithelial cells are an important target for coronavirus infection in the lung, and infected cells can initiate innate immune responses to viral infection. In this overview, we describe in vitro models of highly differentiated alveolar epithelial cells that are currently being used to study the innate immune response to coronavirus infection. We have shown that rat coronavirus infection of rat alveolar type I epithelial cells in vitro induces expression of CXC chemokines, which may recruit and activate neutrophils. Although neutrophils are recruited early in infection in several coronavirus models including rat coronavirus. However, their role in viral clearance and/or immune-mediated tissue damage is not understood. Primary cultures of differentiated alveolar epithelial cells will be useful for identifying the interactions between coronaviruses and alveolar epithelial cells that influence the innate immune responses to infection in the lung. Understanding the molecular details of these interactions will be critical for the design of effective strategies to prevent and treat coronavirus infections in the lung. Oxford University Press 2009-07-28 /pmc/articles/PMC2774885/ /pubmed/19638499 http://dx.doi.org/10.1189/jlb.0209078 Text en © 2009 Society for Leukocyte Biology https://academic.oup.com/pages/standard-publication-reuse-rightsThis article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/pages/standard-publication-reuse-rights) This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Mini-Reviews
Miura, Tanya A
Holmes, Kathryn V
Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title_full Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title_fullStr Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title_full_unstemmed Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title_short Host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
title_sort host-pathogen interactions during coronavirus infection of primary alveolar epithelial cells
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774885/
https://www.ncbi.nlm.nih.gov/pubmed/19638499
http://dx.doi.org/10.1189/jlb.0209078
work_keys_str_mv AT miuratanyaa hostpathogeninteractionsduringcoronavirusinfectionofprimaryalveolarepithelialcells
AT holmeskathrynv hostpathogeninteractionsduringcoronavirusinfectionofprimaryalveolarepithelialcells