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Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells
The primary targets for SARS-CoV infection are the epithelial cells in the respiratory and intestinal tract. The angiotensin-converting enzyme 2 (ACE-2) has been identified as a functional receptor for SARS-CoV. ACE-2 has been shown to be expressed at the apical domain of polarized Calu-3 cells. In...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc. Published by Elsevier Inc.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441846/ https://www.ncbi.nlm.nih.gov/pubmed/18406349 http://dx.doi.org/10.1016/j.bbrc.2008.04.006 |
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author | Kumaki, Yohichi Day, Craig W. Wandersee, Miles K. Schow, Bradley P. Madsen, Justin S. Grant, Dixon Roth, Jason P. Smee, Donald F. Blatt, Lawrence M. Barnard, Dale L. |
author_facet | Kumaki, Yohichi Day, Craig W. Wandersee, Miles K. Schow, Bradley P. Madsen, Justin S. Grant, Dixon Roth, Jason P. Smee, Donald F. Blatt, Lawrence M. Barnard, Dale L. |
author_sort | Kumaki, Yohichi |
collection | PubMed |
description | The primary targets for SARS-CoV infection are the epithelial cells in the respiratory and intestinal tract. The angiotensin-converting enzyme 2 (ACE-2) has been identified as a functional receptor for SARS-CoV. ACE-2 has been shown to be expressed at the apical domain of polarized Calu-3 cells. In this report, interferon alfacon 1 was examined for inhibitory activities against SARS-CoV on human lung carcinoma epithelial Calu-3 cell line and the other three African green monkey kidney epithelial cell lines. Interferon alfacon 1 demonstrated significant antiviral activity in neutral red uptake assay and virus yield reduction assay. The data might provide an important insight into the mechanism of pathogenesis of SARS-CoV allowing further development of antiviral therapies for treating SARS infections. |
format | Text |
id | pubmed-2441846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Inc. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-24418462009-06-20 Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells Kumaki, Yohichi Day, Craig W. Wandersee, Miles K. Schow, Bradley P. Madsen, Justin S. Grant, Dixon Roth, Jason P. Smee, Donald F. Blatt, Lawrence M. Barnard, Dale L. Biochem Biophys Res Commun Article The primary targets for SARS-CoV infection are the epithelial cells in the respiratory and intestinal tract. The angiotensin-converting enzyme 2 (ACE-2) has been identified as a functional receptor for SARS-CoV. ACE-2 has been shown to be expressed at the apical domain of polarized Calu-3 cells. In this report, interferon alfacon 1 was examined for inhibitory activities against SARS-CoV on human lung carcinoma epithelial Calu-3 cell line and the other three African green monkey kidney epithelial cell lines. Interferon alfacon 1 demonstrated significant antiviral activity in neutral red uptake assay and virus yield reduction assay. The data might provide an important insight into the mechanism of pathogenesis of SARS-CoV allowing further development of antiviral therapies for treating SARS infections. Elsevier Inc. Published by Elsevier Inc. 2008-06-20 2008-04-10 /pmc/articles/PMC2441846/ /pubmed/18406349 http://dx.doi.org/10.1016/j.bbrc.2008.04.006 Text en Copyright © 2008 Elsevier Inc. Published by Elsevier Inc. 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 Kumaki, Yohichi Day, Craig W. Wandersee, Miles K. Schow, Bradley P. Madsen, Justin S. Grant, Dixon Roth, Jason P. Smee, Donald F. Blatt, Lawrence M. Barnard, Dale L. Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title | Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title_full | Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title_fullStr | Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title_full_unstemmed | Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title_short | Interferon alfacon 1 inhibits SARS-CoV infection in human bronchial epithelial Calu-3 cells |
title_sort | interferon alfacon 1 inhibits sars-cov infection in human bronchial epithelial calu-3 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441846/ https://www.ncbi.nlm.nih.gov/pubmed/18406349 http://dx.doi.org/10.1016/j.bbrc.2008.04.006 |
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