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Cloning, expression and characterization of ferret CXCL10

Chemokines and their receptors function in the recruitment and activation of cells of the immune system to sites of inflammation. As such, chemokines play an important role in mediating pathophysiological events during microbial infection. In particular, CXCL9, CXCL10 and CXCL11 and their cognate re...

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Autores principales: Danesh, Ali, Seneviratne, Charit, Cameron, Cheryl M., Banner, David, Devries, Mark E., Kelvin, Alyson A., Xu, Luoling, Ran, Longsi, Bosinger, Steven E., Rowe, Thomas, Czub, Marcus, Jonsson, Colleen B., Cameron, Mark J., Kelvin, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653245/
https://www.ncbi.nlm.nih.gov/pubmed/18006061
http://dx.doi.org/10.1016/j.molimm.2007.09.018
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author Danesh, Ali
Seneviratne, Charit
Cameron, Cheryl M.
Banner, David
Devries, Mark E.
Kelvin, Alyson A.
Xu, Luoling
Ran, Longsi
Bosinger, Steven E.
Rowe, Thomas
Czub, Marcus
Jonsson, Colleen B.
Cameron, Mark J.
Kelvin, David J.
author_facet Danesh, Ali
Seneviratne, Charit
Cameron, Cheryl M.
Banner, David
Devries, Mark E.
Kelvin, Alyson A.
Xu, Luoling
Ran, Longsi
Bosinger, Steven E.
Rowe, Thomas
Czub, Marcus
Jonsson, Colleen B.
Cameron, Mark J.
Kelvin, David J.
author_sort Danesh, Ali
collection PubMed
description Chemokines and their receptors function in the recruitment and activation of cells of the immune system to sites of inflammation. As such, chemokines play an important role in mediating pathophysiological events during microbial infection. In particular, CXCL9, CXCL10 and CXCL11 and their cognate receptor CXCR3 have been associated with the clinical course of several infectious diseases, including severe acute respiratory syndrome (SARS) and influenza. While CXCL9, CXCL10 and CXCL11 share the same receptor and have overlapping functions, each can also have unique activity in host defense. The lack of a preferred characterized animal model for SARS has brought our attention to ferrets, which have been used for years in influenza studies. The lack of immunological reagents for ferrets prompted us to clone CXCL9, CXCL10, CXCL11 and CXCR3 and, in the case of CXCL10, to express the gene as a recombinant protein. In this study we demonstrate that endogenous ferret CXCL10 exhibits similar mRNA expression patterns in the lungs of deceased SARS patients and ferrets experimentally infected with SARS coronavirus. This study therefore represents an important step towards development of the ferret as a model for the role of CXCL9, CXCL10 and CXCL11:CXCR3 axis in severe viral infections.
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spelling pubmed-56532452017-10-23 Cloning, expression and characterization of ferret CXCL10 Danesh, Ali Seneviratne, Charit Cameron, Cheryl M. Banner, David Devries, Mark E. Kelvin, Alyson A. Xu, Luoling Ran, Longsi Bosinger, Steven E. Rowe, Thomas Czub, Marcus Jonsson, Colleen B. Cameron, Mark J. Kelvin, David J. Mol Immunol Article Chemokines and their receptors function in the recruitment and activation of cells of the immune system to sites of inflammation. As such, chemokines play an important role in mediating pathophysiological events during microbial infection. In particular, CXCL9, CXCL10 and CXCL11 and their cognate receptor CXCR3 have been associated with the clinical course of several infectious diseases, including severe acute respiratory syndrome (SARS) and influenza. While CXCL9, CXCL10 and CXCL11 share the same receptor and have overlapping functions, each can also have unique activity in host defense. The lack of a preferred characterized animal model for SARS has brought our attention to ferrets, which have been used for years in influenza studies. The lack of immunological reagents for ferrets prompted us to clone CXCL9, CXCL10, CXCL11 and CXCR3 and, in the case of CXCL10, to express the gene as a recombinant protein. In this study we demonstrate that endogenous ferret CXCL10 exhibits similar mRNA expression patterns in the lungs of deceased SARS patients and ferrets experimentally infected with SARS coronavirus. This study therefore represents an important step towards development of the ferret as a model for the role of CXCL9, CXCL10 and CXCL11:CXCR3 axis in severe viral infections. Elsevier Ltd. 2008-03 2007-11-19 /pmc/articles/PMC5653245/ /pubmed/18006061 http://dx.doi.org/10.1016/j.molimm.2007.09.018 Text en Copyright © 2007 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
Danesh, Ali
Seneviratne, Charit
Cameron, Cheryl M.
Banner, David
Devries, Mark E.
Kelvin, Alyson A.
Xu, Luoling
Ran, Longsi
Bosinger, Steven E.
Rowe, Thomas
Czub, Marcus
Jonsson, Colleen B.
Cameron, Mark J.
Kelvin, David J.
Cloning, expression and characterization of ferret CXCL10
title Cloning, expression and characterization of ferret CXCL10
title_full Cloning, expression and characterization of ferret CXCL10
title_fullStr Cloning, expression and characterization of ferret CXCL10
title_full_unstemmed Cloning, expression and characterization of ferret CXCL10
title_short Cloning, expression and characterization of ferret CXCL10
title_sort cloning, expression and characterization of ferret cxcl10
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653245/
https://www.ncbi.nlm.nih.gov/pubmed/18006061
http://dx.doi.org/10.1016/j.molimm.2007.09.018
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