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Recent advances in lung organoid development and applications in disease modeling
Over the last decade, several organoid models have evolved to acquire increasing cellular, structural, and functional complexity. Advanced lung organoid platforms derived from various sources, including adult, fetal, and induced pluripotent stem cells, have now been generated, which more closely mim...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645385/ https://www.ncbi.nlm.nih.gov/pubmed/37966116 http://dx.doi.org/10.1172/JCI170500 |
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author | Vazquez-Armendariz, Ana I. Tata, Purushothama Rao |
author_facet | Vazquez-Armendariz, Ana I. Tata, Purushothama Rao |
author_sort | Vazquez-Armendariz, Ana I. |
collection | PubMed |
description | Over the last decade, several organoid models have evolved to acquire increasing cellular, structural, and functional complexity. Advanced lung organoid platforms derived from various sources, including adult, fetal, and induced pluripotent stem cells, have now been generated, which more closely mimic the cellular architecture found within the airways and alveoli. In this regard, the establishment of novel protocols with optimized stem cell isolation and culture conditions has given rise to an array of models able to study key cellular and molecular players involved in lung injury and repair. In addition, introduction of other nonepithelial cellular components, such as immune, mesenchymal, and endothelial cells, and employment of novel precision gene editing tools have further broadened the range of applications for these systems by providing a microenvironment and/or phenotype closer to the desired in vivo scenario. Thus, these developments in organoid technology have enhanced our ability to model various aspects of lung biology, including pathogenesis of diseases such as chronic obstructive pulmonary disease, pulmonary fibrosis, cystic fibrosis, and infectious disease and host-microbe interactions, in ways that are often difficult to undertake using only in vivo models. In this Review, we summarize the latest developments in lung organoid technology and their applicability for disease modeling and outline their strengths, drawbacks, and potential avenues for future development. |
format | Online Article Text |
id | pubmed-10645385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-106453852023-11-15 Recent advances in lung organoid development and applications in disease modeling Vazquez-Armendariz, Ana I. Tata, Purushothama Rao J Clin Invest Review Series Over the last decade, several organoid models have evolved to acquire increasing cellular, structural, and functional complexity. Advanced lung organoid platforms derived from various sources, including adult, fetal, and induced pluripotent stem cells, have now been generated, which more closely mimic the cellular architecture found within the airways and alveoli. In this regard, the establishment of novel protocols with optimized stem cell isolation and culture conditions has given rise to an array of models able to study key cellular and molecular players involved in lung injury and repair. In addition, introduction of other nonepithelial cellular components, such as immune, mesenchymal, and endothelial cells, and employment of novel precision gene editing tools have further broadened the range of applications for these systems by providing a microenvironment and/or phenotype closer to the desired in vivo scenario. Thus, these developments in organoid technology have enhanced our ability to model various aspects of lung biology, including pathogenesis of diseases such as chronic obstructive pulmonary disease, pulmonary fibrosis, cystic fibrosis, and infectious disease and host-microbe interactions, in ways that are often difficult to undertake using only in vivo models. In this Review, we summarize the latest developments in lung organoid technology and their applicability for disease modeling and outline their strengths, drawbacks, and potential avenues for future development. American Society for Clinical Investigation 2023-11-15 /pmc/articles/PMC10645385/ /pubmed/37966116 http://dx.doi.org/10.1172/JCI170500 Text en © 2023 Vazquez-Armendariz, et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Series Vazquez-Armendariz, Ana I. Tata, Purushothama Rao Recent advances in lung organoid development and applications in disease modeling |
title | Recent advances in lung organoid development and applications in disease modeling |
title_full | Recent advances in lung organoid development and applications in disease modeling |
title_fullStr | Recent advances in lung organoid development and applications in disease modeling |
title_full_unstemmed | Recent advances in lung organoid development and applications in disease modeling |
title_short | Recent advances in lung organoid development and applications in disease modeling |
title_sort | recent advances in lung organoid development and applications in disease modeling |
topic | Review Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645385/ https://www.ncbi.nlm.nih.gov/pubmed/37966116 http://dx.doi.org/10.1172/JCI170500 |
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