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Production of amphiregulin and recovery from influenza is greater in males than females

BACKGROUND: Amphiregulin (AREG) is an epidermal growth factor that is a significant mediator of tissue repair at mucosal sites, including in the lungs during influenza A virus (IAV) infection. Previous research illustrates that males of reproductive ages experience less severe disease and recover fa...

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Autores principales: Vermillion, Meghan S., Ursin, Rebecca L., Kuok, Denise I. T., vom Steeg, Landon G., Wohlgemuth, Nicholas, Hall, Olivia J., Fink, Ashley L., Sasse, Eric, Nelson, Andrew, Ndeh, Roland, McGrath-Morrow, Sharon, Mitzner, Wayne, Chan, Michael C. W., Pekosz, Andrew, Klein, Sabra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048771/
https://www.ncbi.nlm.nih.gov/pubmed/30012205
http://dx.doi.org/10.1186/s13293-018-0184-8
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author Vermillion, Meghan S.
Ursin, Rebecca L.
Kuok, Denise I. T.
vom Steeg, Landon G.
Wohlgemuth, Nicholas
Hall, Olivia J.
Fink, Ashley L.
Sasse, Eric
Nelson, Andrew
Ndeh, Roland
McGrath-Morrow, Sharon
Mitzner, Wayne
Chan, Michael C. W.
Pekosz, Andrew
Klein, Sabra L.
author_facet Vermillion, Meghan S.
Ursin, Rebecca L.
Kuok, Denise I. T.
vom Steeg, Landon G.
Wohlgemuth, Nicholas
Hall, Olivia J.
Fink, Ashley L.
Sasse, Eric
Nelson, Andrew
Ndeh, Roland
McGrath-Morrow, Sharon
Mitzner, Wayne
Chan, Michael C. W.
Pekosz, Andrew
Klein, Sabra L.
author_sort Vermillion, Meghan S.
collection PubMed
description BACKGROUND: Amphiregulin (AREG) is an epidermal growth factor that is a significant mediator of tissue repair at mucosal sites, including in the lungs during influenza A virus (IAV) infection. Previous research illustrates that males of reproductive ages experience less severe disease and recover faster than females following infection with IAV. METHODS: Whether males and females differentially produce and utilize AREG for pulmonary repair after IAV infection was investigated using murine models on a C57BL/6 background and primary mouse and human epithelial cell culture systems. RESULTS: Following sublethal infection with 2009 H1N1 IAV, adult female mice experienced greater morbidity and pulmonary inflammation during the acute phase of infection as well as worse pulmonary function during the recovery phase of infection than males, despite having similar virus clearance kinetics. As compared with females, AREG expression was greater in the lungs of male mice as well as in primary respiratory epithelial cells derived from mouse and human male donors, in response to H1N1 IAVs. Internalization of the epidermal growth factor receptor (EGFR) was also greater in respiratory epithelial cells derived from male than female mice. IAV infection of Areg knock-out (Areg(−/−)) mice eliminated sex differences in IAV pathogenesis, with a more significant role for AREG in infection of male compared to female mice. Deletion of Areg had no effect on virus replication kinetics in either sex. Gonadectomy and treatment of either wild-type or Areg(−/−) males with testosterone improved the outcome of IAV as compared with their placebo-treated conspecifics. CONCLUSIONS: Taken together, these data show that elevated levels of testosterone and AREG, either independently or in combination, improve resilience (i.e., repair and recovery of damaged tissue) and contribute to better influenza outcomes in males compared with females.
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spelling pubmed-60487712018-07-19 Production of amphiregulin and recovery from influenza is greater in males than females Vermillion, Meghan S. Ursin, Rebecca L. Kuok, Denise I. T. vom Steeg, Landon G. Wohlgemuth, Nicholas Hall, Olivia J. Fink, Ashley L. Sasse, Eric Nelson, Andrew Ndeh, Roland McGrath-Morrow, Sharon Mitzner, Wayne Chan, Michael C. W. Pekosz, Andrew Klein, Sabra L. Biol Sex Differ Research BACKGROUND: Amphiregulin (AREG) is an epidermal growth factor that is a significant mediator of tissue repair at mucosal sites, including in the lungs during influenza A virus (IAV) infection. Previous research illustrates that males of reproductive ages experience less severe disease and recover faster than females following infection with IAV. METHODS: Whether males and females differentially produce and utilize AREG for pulmonary repair after IAV infection was investigated using murine models on a C57BL/6 background and primary mouse and human epithelial cell culture systems. RESULTS: Following sublethal infection with 2009 H1N1 IAV, adult female mice experienced greater morbidity and pulmonary inflammation during the acute phase of infection as well as worse pulmonary function during the recovery phase of infection than males, despite having similar virus clearance kinetics. As compared with females, AREG expression was greater in the lungs of male mice as well as in primary respiratory epithelial cells derived from mouse and human male donors, in response to H1N1 IAVs. Internalization of the epidermal growth factor receptor (EGFR) was also greater in respiratory epithelial cells derived from male than female mice. IAV infection of Areg knock-out (Areg(−/−)) mice eliminated sex differences in IAV pathogenesis, with a more significant role for AREG in infection of male compared to female mice. Deletion of Areg had no effect on virus replication kinetics in either sex. Gonadectomy and treatment of either wild-type or Areg(−/−) males with testosterone improved the outcome of IAV as compared with their placebo-treated conspecifics. CONCLUSIONS: Taken together, these data show that elevated levels of testosterone and AREG, either independently or in combination, improve resilience (i.e., repair and recovery of damaged tissue) and contribute to better influenza outcomes in males compared with females. BioMed Central 2018-07-17 /pmc/articles/PMC6048771/ /pubmed/30012205 http://dx.doi.org/10.1186/s13293-018-0184-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Vermillion, Meghan S.
Ursin, Rebecca L.
Kuok, Denise I. T.
vom Steeg, Landon G.
Wohlgemuth, Nicholas
Hall, Olivia J.
Fink, Ashley L.
Sasse, Eric
Nelson, Andrew
Ndeh, Roland
McGrath-Morrow, Sharon
Mitzner, Wayne
Chan, Michael C. W.
Pekosz, Andrew
Klein, Sabra L.
Production of amphiregulin and recovery from influenza is greater in males than females
title Production of amphiregulin and recovery from influenza is greater in males than females
title_full Production of amphiregulin and recovery from influenza is greater in males than females
title_fullStr Production of amphiregulin and recovery from influenza is greater in males than females
title_full_unstemmed Production of amphiregulin and recovery from influenza is greater in males than females
title_short Production of amphiregulin and recovery from influenza is greater in males than females
title_sort production of amphiregulin and recovery from influenza is greater in males than females
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048771/
https://www.ncbi.nlm.nih.gov/pubmed/30012205
http://dx.doi.org/10.1186/s13293-018-0184-8
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