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Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection()
Respiratory syncytial virus (RSV) replication is primarily limited to the upper respiratory tract epithelium and primary, differentiated normal human bronchial epithelial cells (NHBE) have, therefore, been considered a good system for in vitro analysis of lung tissue response to respiratory virus in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier/North-Holland Biomedical Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112923/ https://www.ncbi.nlm.nih.gov/pubmed/21458491 http://dx.doi.org/10.1016/j.jviromet.2011.03.027 |
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author | Harcourt, Jennifer L. Caidi, Hayat Anderson, Larry J. Haynes, Lia M. |
author_facet | Harcourt, Jennifer L. Caidi, Hayat Anderson, Larry J. Haynes, Lia M. |
author_sort | Harcourt, Jennifer L. |
collection | PubMed |
description | Respiratory syncytial virus (RSV) replication is primarily limited to the upper respiratory tract epithelium and primary, differentiated normal human bronchial epithelial cells (NHBE) have, therefore, been considered a good system for in vitro analysis of lung tissue response to respiratory virus infection and virus–host interactions. However, NHBE cells are expensive, difficult to culture, and vary with the source patient. An alternate approach is to use a continuous cell line that has features of bronchial epithelial cells such as Calu-3, an epithelial cell line derived from human lung adenocarcinoma, as an in vitro model of respiratory virus infection. The results show that Calu-3 fully polarize when grown on permeable supports as liquid-covered cultures. Polarized Calu-3 are susceptible to RSV infection and release infectious virus primarily from the apical surface, consistent with studies in NHBE cells. The data demonstrate that polarized Calu-3 may serve as a useful in vitro model to study host responses to RSV infection. |
format | Online Article Text |
id | pubmed-7112923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier/North-Holland Biomedical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71129232020-04-02 Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() Harcourt, Jennifer L. Caidi, Hayat Anderson, Larry J. Haynes, Lia M. J Virol Methods Short Communication Respiratory syncytial virus (RSV) replication is primarily limited to the upper respiratory tract epithelium and primary, differentiated normal human bronchial epithelial cells (NHBE) have, therefore, been considered a good system for in vitro analysis of lung tissue response to respiratory virus infection and virus–host interactions. However, NHBE cells are expensive, difficult to culture, and vary with the source patient. An alternate approach is to use a continuous cell line that has features of bronchial epithelial cells such as Calu-3, an epithelial cell line derived from human lung adenocarcinoma, as an in vitro model of respiratory virus infection. The results show that Calu-3 fully polarize when grown on permeable supports as liquid-covered cultures. Polarized Calu-3 are susceptible to RSV infection and release infectious virus primarily from the apical surface, consistent with studies in NHBE cells. The data demonstrate that polarized Calu-3 may serve as a useful in vitro model to study host responses to RSV infection. Elsevier/North-Holland Biomedical Press 2011-06 2011-03-31 /pmc/articles/PMC7112923/ /pubmed/21458491 http://dx.doi.org/10.1016/j.jviromet.2011.03.027 Text en 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 | Short Communication Harcourt, Jennifer L. Caidi, Hayat Anderson, Larry J. Haynes, Lia M. Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title | Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title_full | Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title_fullStr | Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title_full_unstemmed | Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title_short | Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
title_sort | evaluation of the calu-3 cell line as a model of in vitro respiratory syncytial virus infection() |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112923/ https://www.ncbi.nlm.nih.gov/pubmed/21458491 http://dx.doi.org/10.1016/j.jviromet.2011.03.027 |
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