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Lung viral infection modelling in a bioengineered whole-organ

Lung infections are one of the leading causes of death worldwide, and this situation has been exacerbated by the emergence of COVID-19. Pre-clinical modelling of viral infections has relied on cell cultures that lack 3D structure and the context of lung extracellular matrices. Here, we propose a bio...

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Autores principales: Tommasini, Fabio, Benoist, Thomas, Shibuya, Soichi, Woodall, Maximillian N.J., Naldi, Eleonora, Palor, Machaela, Orr, Jessica C., Giobbe, Giovanni Giuseppe, Maughan, Elizabeth F., Saleh, Tarek, Gjinovci, Asllan, Hutchinson, J. Ciaran, Arthurs, Owen J., Janes, Sam M., Elvassore, Nicola, Hynds, Robert E., Smith, Claire M., Michielin, Federica, Pellegata, Alessandro Filippo, De Coppi, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281738/
https://www.ncbi.nlm.nih.gov/pubmed/37515903
http://dx.doi.org/10.1016/j.biomaterials.2023.122203
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author Tommasini, Fabio
Benoist, Thomas
Shibuya, Soichi
Woodall, Maximillian N.J.
Naldi, Eleonora
Palor, Machaela
Orr, Jessica C.
Giobbe, Giovanni Giuseppe
Maughan, Elizabeth F.
Saleh, Tarek
Gjinovci, Asllan
Hutchinson, J. Ciaran
Arthurs, Owen J.
Janes, Sam M.
Elvassore, Nicola
Hynds, Robert E.
Smith, Claire M.
Michielin, Federica
Pellegata, Alessandro Filippo
De Coppi, Paolo
author_facet Tommasini, Fabio
Benoist, Thomas
Shibuya, Soichi
Woodall, Maximillian N.J.
Naldi, Eleonora
Palor, Machaela
Orr, Jessica C.
Giobbe, Giovanni Giuseppe
Maughan, Elizabeth F.
Saleh, Tarek
Gjinovci, Asllan
Hutchinson, J. Ciaran
Arthurs, Owen J.
Janes, Sam M.
Elvassore, Nicola
Hynds, Robert E.
Smith, Claire M.
Michielin, Federica
Pellegata, Alessandro Filippo
De Coppi, Paolo
author_sort Tommasini, Fabio
collection PubMed
description Lung infections are one of the leading causes of death worldwide, and this situation has been exacerbated by the emergence of COVID-19. Pre-clinical modelling of viral infections has relied on cell cultures that lack 3D structure and the context of lung extracellular matrices. Here, we propose a bioreactor-based, whole-organ lung model of viral infection. The bioreactor takes advantage of an automated system to achieve efficient decellularization of a whole rat lung, and recellularization of the scaffold using primary human bronchial cells. Automatization allowed for the dynamic culture of airway epithelial cells in a breathing-mimicking setup that led to an even distribution of lung epithelial cells throughout the distal regions. In the sealed bioreactor system, we demonstrate proof-of-concept for viral infection within the epithelialized lung by infecting primary human airway epithelial cells and subsequently injecting neutrophils. Moreover, to assess the possibility of drug screening in this model, we demonstrate the efficacy of the broad-spectrum antiviral remdesivir. This whole-organ scale lung infection model represents a step towards modelling viral infection of human cells in a 3D context, providing a powerful tool to investigate the mechanisms of the early stages of pathogenic infections and the development of effective treatment strategies for respiratory diseases.
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spelling pubmed-102817382023-06-21 Lung viral infection modelling in a bioengineered whole-organ Tommasini, Fabio Benoist, Thomas Shibuya, Soichi Woodall, Maximillian N.J. Naldi, Eleonora Palor, Machaela Orr, Jessica C. Giobbe, Giovanni Giuseppe Maughan, Elizabeth F. Saleh, Tarek Gjinovci, Asllan Hutchinson, J. Ciaran Arthurs, Owen J. Janes, Sam M. Elvassore, Nicola Hynds, Robert E. Smith, Claire M. Michielin, Federica Pellegata, Alessandro Filippo De Coppi, Paolo Biomaterials Article Lung infections are one of the leading causes of death worldwide, and this situation has been exacerbated by the emergence of COVID-19. Pre-clinical modelling of viral infections has relied on cell cultures that lack 3D structure and the context of lung extracellular matrices. Here, we propose a bioreactor-based, whole-organ lung model of viral infection. The bioreactor takes advantage of an automated system to achieve efficient decellularization of a whole rat lung, and recellularization of the scaffold using primary human bronchial cells. Automatization allowed for the dynamic culture of airway epithelial cells in a breathing-mimicking setup that led to an even distribution of lung epithelial cells throughout the distal regions. In the sealed bioreactor system, we demonstrate proof-of-concept for viral infection within the epithelialized lung by infecting primary human airway epithelial cells and subsequently injecting neutrophils. Moreover, to assess the possibility of drug screening in this model, we demonstrate the efficacy of the broad-spectrum antiviral remdesivir. This whole-organ scale lung infection model represents a step towards modelling viral infection of human cells in a 3D context, providing a powerful tool to investigate the mechanisms of the early stages of pathogenic infections and the development of effective treatment strategies for respiratory diseases. Published by Elsevier Ltd. 2023-06-21 /pmc/articles/PMC10281738/ /pubmed/37515903 http://dx.doi.org/10.1016/j.biomaterials.2023.122203 Text en © 2023 Published by Elsevier Ltd. 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
Tommasini, Fabio
Benoist, Thomas
Shibuya, Soichi
Woodall, Maximillian N.J.
Naldi, Eleonora
Palor, Machaela
Orr, Jessica C.
Giobbe, Giovanni Giuseppe
Maughan, Elizabeth F.
Saleh, Tarek
Gjinovci, Asllan
Hutchinson, J. Ciaran
Arthurs, Owen J.
Janes, Sam M.
Elvassore, Nicola
Hynds, Robert E.
Smith, Claire M.
Michielin, Federica
Pellegata, Alessandro Filippo
De Coppi, Paolo
Lung viral infection modelling in a bioengineered whole-organ
title Lung viral infection modelling in a bioengineered whole-organ
title_full Lung viral infection modelling in a bioengineered whole-organ
title_fullStr Lung viral infection modelling in a bioengineered whole-organ
title_full_unstemmed Lung viral infection modelling in a bioengineered whole-organ
title_short Lung viral infection modelling in a bioengineered whole-organ
title_sort lung viral infection modelling in a bioengineered whole-organ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281738/
https://www.ncbi.nlm.nih.gov/pubmed/37515903
http://dx.doi.org/10.1016/j.biomaterials.2023.122203
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