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Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors
Recombinant, replication-deficient serotype 5 adenovirus infects the liver upon in vivo, systemic injection in rodents. This infection requires the binding of factor X to the capsid of this adenovirus. Another organ, the adrenal gland is also infected upon systemic administration of Ad, however, whe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636216/ https://www.ncbi.nlm.nih.gov/pubmed/23638001 http://dx.doi.org/10.1371/journal.pone.0062191 |
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author | Tran, Lucile Ouisse, Laure-Hélène Richard-Fiardo, Peggy Franken, Philippe R. Darcourt, Jacques Cornilleau, Gaétan Benihoud, Karim Vassaux, Georges |
author_facet | Tran, Lucile Ouisse, Laure-Hélène Richard-Fiardo, Peggy Franken, Philippe R. Darcourt, Jacques Cornilleau, Gaétan Benihoud, Karim Vassaux, Georges |
author_sort | Tran, Lucile |
collection | PubMed |
description | Recombinant, replication-deficient serotype 5 adenovirus infects the liver upon in vivo, systemic injection in rodents. This infection requires the binding of factor X to the capsid of this adenovirus. Another organ, the adrenal gland is also infected upon systemic administration of Ad, however, whether this infection is dependent on the cocksackie adenovirus receptor (CAR) or depends on the binding of factor X to the viral capsid remained to be determined. In the present work, we have used a pharmacological agent (warfarin) as well as recombinant adenoviruses lacking the binding site of Factor X to elucidate this mechanism in mice. We demonstrate that, as observed in the liver, adenovirus infection of the adrenal glands in vivo requires Factor X. Considering that the level of transduction of the adrenal glands is well-below that of the liver and that capsid-modified adenoviruses are unlikely to selectively infect the adrenal glands, we have used single-photon emission computed tomography (SPECT) imaging of gene expression to determine whether local virus administration (direct injection in the kidney) could increase gene transfer to the adrenal glands. We demonstrate that direct injection of the virus in the kidney increases gene transfer in the adrenal gland but liver transduction remains important. These observations strongly suggest that serotype 5 adenovirus uses a similar mechanism to infect liver and adrenal gland and that selective transgene expression in the latter is more likely to be achieved through transcriptional targeting. |
format | Online Article Text |
id | pubmed-3636216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36362162013-05-01 Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors Tran, Lucile Ouisse, Laure-Hélène Richard-Fiardo, Peggy Franken, Philippe R. Darcourt, Jacques Cornilleau, Gaétan Benihoud, Karim Vassaux, Georges PLoS One Research Article Recombinant, replication-deficient serotype 5 adenovirus infects the liver upon in vivo, systemic injection in rodents. This infection requires the binding of factor X to the capsid of this adenovirus. Another organ, the adrenal gland is also infected upon systemic administration of Ad, however, whether this infection is dependent on the cocksackie adenovirus receptor (CAR) or depends on the binding of factor X to the viral capsid remained to be determined. In the present work, we have used a pharmacological agent (warfarin) as well as recombinant adenoviruses lacking the binding site of Factor X to elucidate this mechanism in mice. We demonstrate that, as observed in the liver, adenovirus infection of the adrenal glands in vivo requires Factor X. Considering that the level of transduction of the adrenal glands is well-below that of the liver and that capsid-modified adenoviruses are unlikely to selectively infect the adrenal glands, we have used single-photon emission computed tomography (SPECT) imaging of gene expression to determine whether local virus administration (direct injection in the kidney) could increase gene transfer to the adrenal glands. We demonstrate that direct injection of the virus in the kidney increases gene transfer in the adrenal gland but liver transduction remains important. These observations strongly suggest that serotype 5 adenovirus uses a similar mechanism to infect liver and adrenal gland and that selective transgene expression in the latter is more likely to be achieved through transcriptional targeting. Public Library of Science 2013-04-25 /pmc/articles/PMC3636216/ /pubmed/23638001 http://dx.doi.org/10.1371/journal.pone.0062191 Text en © 2013 Tran et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tran, Lucile Ouisse, Laure-Hélène Richard-Fiardo, Peggy Franken, Philippe R. Darcourt, Jacques Cornilleau, Gaétan Benihoud, Karim Vassaux, Georges Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title | Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title_full | Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title_fullStr | Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title_full_unstemmed | Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title_short | Adrenal Gland Infection by Serotype 5 Adenovirus Requires Coagulation Factors |
title_sort | adrenal gland infection by serotype 5 adenovirus requires coagulation factors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636216/ https://www.ncbi.nlm.nih.gov/pubmed/23638001 http://dx.doi.org/10.1371/journal.pone.0062191 |
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