The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model

Human and mouse respiratory tracts show anatomical and physiological differences, which will benefit from alternative experimental models for studying many respiratory diseases. Pig has been recognized as a valuable biomedical model, in particular for lung transplantation or pathologies such as cystic fibrosis and influenza infection. However, there is a lack of knowledge about the porcine respiratory immune system. Here we segregated and studied six populations of pig lung dendritic cells (DCs)/macrophages (Mθs) as follows conventional DCs (cDC) 1 and cDC2, inflammatory monocyte-derived DCs (moDCs), monocyte-derived Mθs, and interstitial and alveolar Mθs. The three DC subsets present migratory and naive T-cell stimulation capacities. As observed in human and mice, porcine cDC1 and cDC2 were able to induce T-helper (Th)1 and Th2 responses, respectively. Interestingly, porcine moDCs increased in the lung upon influenza infection, as observed in the mouse model. Pig cDC2 shared some characteristics observed in human but not in mice, such as the expression of FCϵRI and Langerin, and an intra-epithelial localization. This work, by unraveling the extended similarities of the porcine and human lung DC/Mθ networks, highlights the relevance of pig, both as an exploratory model of DC/Mθ functions and as a model for human inflammatory lung pathologies.

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Main Authors: Maisonnasse, P., Bouguyon, E., Piton, G., Ezquerra Martínez, Ángel, Urien, C., Deloizy, C., Bourge, M., Leplat, J. J., Simon, G., Chevalier, C., Vincent-Naulleau, S., Crisci, E., Montoya, M., Schwartz-Cornil, I., Bertho, N.
Format: journal article biblioteca
Language:English
Published: Springer Nature 2016
Online Access:http://hdl.handle.net/20.500.12792/2576
http://hdl.handle.net/10261/293462
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spelling dig-inia-es-10261-2934622023-02-20T10:28:46Z The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model Maisonnasse, P. Bouguyon, E. Piton, G. Ezquerra Martínez, Ángel Urien, C. Deloizy, C. Bourge, M. Leplat, J. J. Simon, G. Chevalier, C. Vincent-Naulleau, S. Crisci, E. Montoya, M. Schwartz-Cornil, I. Bertho, N. Human and mouse respiratory tracts show anatomical and physiological differences, which will benefit from alternative experimental models for studying many respiratory diseases. Pig has been recognized as a valuable biomedical model, in particular for lung transplantation or pathologies such as cystic fibrosis and influenza infection. However, there is a lack of knowledge about the porcine respiratory immune system. Here we segregated and studied six populations of pig lung dendritic cells (DCs)/macrophages (Mθs) as follows conventional DCs (cDC) 1 and cDC2, inflammatory monocyte-derived DCs (moDCs), monocyte-derived Mθs, and interstitial and alveolar Mθs. The three DC subsets present migratory and naive T-cell stimulation capacities. As observed in human and mice, porcine cDC1 and cDC2 were able to induce T-helper (Th)1 and Th2 responses, respectively. Interestingly, porcine moDCs increased in the lung upon influenza infection, as observed in the mouse model. Pig cDC2 shared some characteristics observed in human but not in mice, such as the expression of FCϵRI and Langerin, and an intra-epithelial localization. This work, by unraveling the extended similarities of the porcine and human lung DC/Mθ networks, highlights the relevance of pig, both as an exploratory model of DC/Mθ functions and as a model for human inflammatory lung pathologies. 2023-02-20T10:28:46Z 2023-02-20T10:28:46Z 2016 journal article Mucosal Immunology 9: 835-849 (2016) 1933-0219 http://hdl.handle.net/20.500.12792/2576 http://hdl.handle.net/10261/293462 10.1038/mi.2015.105 1935-3456 en none Springer Nature
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language English
description Human and mouse respiratory tracts show anatomical and physiological differences, which will benefit from alternative experimental models for studying many respiratory diseases. Pig has been recognized as a valuable biomedical model, in particular for lung transplantation or pathologies such as cystic fibrosis and influenza infection. However, there is a lack of knowledge about the porcine respiratory immune system. Here we segregated and studied six populations of pig lung dendritic cells (DCs)/macrophages (Mθs) as follows conventional DCs (cDC) 1 and cDC2, inflammatory monocyte-derived DCs (moDCs), monocyte-derived Mθs, and interstitial and alveolar Mθs. The three DC subsets present migratory and naive T-cell stimulation capacities. As observed in human and mice, porcine cDC1 and cDC2 were able to induce T-helper (Th)1 and Th2 responses, respectively. Interestingly, porcine moDCs increased in the lung upon influenza infection, as observed in the mouse model. Pig cDC2 shared some characteristics observed in human but not in mice, such as the expression of FCϵRI and Langerin, and an intra-epithelial localization. This work, by unraveling the extended similarities of the porcine and human lung DC/Mθ networks, highlights the relevance of pig, both as an exploratory model of DC/Mθ functions and as a model for human inflammatory lung pathologies.
format journal article
author Maisonnasse, P.
Bouguyon, E.
Piton, G.
Ezquerra Martínez, Ángel
Urien, C.
Deloizy, C.
Bourge, M.
Leplat, J. J.
Simon, G.
Chevalier, C.
Vincent-Naulleau, S.
Crisci, E.
Montoya, M.
Schwartz-Cornil, I.
Bertho, N.
spellingShingle Maisonnasse, P.
Bouguyon, E.
Piton, G.
Ezquerra Martínez, Ángel
Urien, C.
Deloizy, C.
Bourge, M.
Leplat, J. J.
Simon, G.
Chevalier, C.
Vincent-Naulleau, S.
Crisci, E.
Montoya, M.
Schwartz-Cornil, I.
Bertho, N.
The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
author_facet Maisonnasse, P.
Bouguyon, E.
Piton, G.
Ezquerra Martínez, Ángel
Urien, C.
Deloizy, C.
Bourge, M.
Leplat, J. J.
Simon, G.
Chevalier, C.
Vincent-Naulleau, S.
Crisci, E.
Montoya, M.
Schwartz-Cornil, I.
Bertho, N.
author_sort Maisonnasse, P.
title The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
title_short The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
title_full The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
title_fullStr The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
title_full_unstemmed The respiratory DC/macrophage network at steady-state and upon influenza infection in the swine biomedical model
title_sort respiratory dc/macrophage network at steady-state and upon influenza infection in the swine biomedical model
publisher Springer Nature
publishDate 2016
url http://hdl.handle.net/20.500.12792/2576
http://hdl.handle.net/10261/293462
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