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Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs

Airway organoids are polarized 3D epithelial structures that recapitulate the organization and many of the key functions of the in vivo tissue. They present an attractive model that can overcome some of the limitations of traditional 2D and Air–Liquid Interface (ALI) models, yet the limited accessib...

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Autores principales: Stroulios, Georgios, Brown, Tyler, Moreni, Giulia, Kondro, Douglas, Dei, Alessandro, Eaves, Allen, Louis, Sharon, Hou, Juan, Chang, Wing, Pajkrt, Dasja, Wolthers, Katja C., Sridhar, Adithya, Simmini, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089294/
https://www.ncbi.nlm.nih.gov/pubmed/35538146
http://dx.doi.org/10.1038/s41598-022-11700-z
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author Stroulios, Georgios
Brown, Tyler
Moreni, Giulia
Kondro, Douglas
Dei, Alessandro
Eaves, Allen
Louis, Sharon
Hou, Juan
Chang, Wing
Pajkrt, Dasja
Wolthers, Katja C.
Sridhar, Adithya
Simmini, Salvatore
author_facet Stroulios, Georgios
Brown, Tyler
Moreni, Giulia
Kondro, Douglas
Dei, Alessandro
Eaves, Allen
Louis, Sharon
Hou, Juan
Chang, Wing
Pajkrt, Dasja
Wolthers, Katja C.
Sridhar, Adithya
Simmini, Salvatore
author_sort Stroulios, Georgios
collection PubMed
description Airway organoids are polarized 3D epithelial structures that recapitulate the organization and many of the key functions of the in vivo tissue. They present an attractive model that can overcome some of the limitations of traditional 2D and Air–Liquid Interface (ALI) models, yet the limited accessibility of the organoids’ apical side has hindered their applications in studies focusing on host–pathogen interactions. Here, we describe a scalable, fast and efficient way to generate airway organoids with the apical side externally exposed. These apical-out airway organoids are generated in an Extracellular Matrix (ECM)-free environment from 2D-expanded bronchial epithelial cells and differentiated in suspension to develop uniformly-sized organoid cultures with robust ciliogenesis. Differentiated apical-out airway organoids are susceptible to infection with common respiratory viruses and show varying responses upon treatment with antivirals. In addition to the ease of apical accessibility, these apical-out airway organoids offer an alternative in vitro model to study host–pathogen interactions in higher throughput than the traditional air–liquid interface model.
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spelling pubmed-90892942022-05-10 Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs Stroulios, Georgios Brown, Tyler Moreni, Giulia Kondro, Douglas Dei, Alessandro Eaves, Allen Louis, Sharon Hou, Juan Chang, Wing Pajkrt, Dasja Wolthers, Katja C. Sridhar, Adithya Simmini, Salvatore Sci Rep Article Airway organoids are polarized 3D epithelial structures that recapitulate the organization and many of the key functions of the in vivo tissue. They present an attractive model that can overcome some of the limitations of traditional 2D and Air–Liquid Interface (ALI) models, yet the limited accessibility of the organoids’ apical side has hindered their applications in studies focusing on host–pathogen interactions. Here, we describe a scalable, fast and efficient way to generate airway organoids with the apical side externally exposed. These apical-out airway organoids are generated in an Extracellular Matrix (ECM)-free environment from 2D-expanded bronchial epithelial cells and differentiated in suspension to develop uniformly-sized organoid cultures with robust ciliogenesis. Differentiated apical-out airway organoids are susceptible to infection with common respiratory viruses and show varying responses upon treatment with antivirals. In addition to the ease of apical accessibility, these apical-out airway organoids offer an alternative in vitro model to study host–pathogen interactions in higher throughput than the traditional air–liquid interface model. Nature Publishing Group UK 2022-05-10 /pmc/articles/PMC9089294/ /pubmed/35538146 http://dx.doi.org/10.1038/s41598-022-11700-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Stroulios, Georgios
Brown, Tyler
Moreni, Giulia
Kondro, Douglas
Dei, Alessandro
Eaves, Allen
Louis, Sharon
Hou, Juan
Chang, Wing
Pajkrt, Dasja
Wolthers, Katja C.
Sridhar, Adithya
Simmini, Salvatore
Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title_full Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title_fullStr Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title_full_unstemmed Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title_short Apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
title_sort apical-out airway organoids as a platform for studying viral infections and screening for antiviral drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089294/
https://www.ncbi.nlm.nih.gov/pubmed/35538146
http://dx.doi.org/10.1038/s41598-022-11700-z
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