Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods

Lung diseases rank third in terms of mortality and represent a significant economic burden globally. Scientists have been conducting research to better understand respiratory diseases and find treatments for them. An ideal in vitro model must mimic the in vivo organ structure, physiology, and pathol...

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Main Authors: Krishan Gopal Jain, Nan Miles Xi, Runzhen Zhao, Waqas Ahmad, Gibran Ali, Hong-Long Ji
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/11/11/3034
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author Krishan Gopal Jain
Nan Miles Xi
Runzhen Zhao
Waqas Ahmad
Gibran Ali
Hong-Long Ji
author_facet Krishan Gopal Jain
Nan Miles Xi
Runzhen Zhao
Waqas Ahmad
Gibran Ali
Hong-Long Ji
author_sort Krishan Gopal Jain
collection DOAJ
description Lung diseases rank third in terms of mortality and represent a significant economic burden globally. Scientists have been conducting research to better understand respiratory diseases and find treatments for them. An ideal in vitro model must mimic the in vivo organ structure, physiology, and pathology. Organoids are self-organizing, three-dimensional (3D) structures originating from adult stem cells, embryonic lung bud progenitors, embryonic stem cells (ESCs), and induced pluripotent stem cells (iPSCs). These 3D organoid cultures may provide a platform for exploring tissue development, the regulatory mechanisms related to the repair of lung epithelia, pathophysiological and immunomodulatory responses to different respiratory conditions, and screening compounds for new drugs. To create 3D lung organoids in vitro, both co-culture and feeder-free methods have been used. However, there exists substantial heterogeneity in the organoid culture methods, including the sources of AT2 cells, media composition, and feeder cell origins. This article highlights the currently available methods for growing AT2 organoids and prospective improvements to improve the available culture techniques/conditions. Further, we discuss various applications, particularly those aimed at modeling human distal lung diseases and cell therapy.
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spelling doaj.art-45b7e95df37440f79db0be0251a7e8912023-11-24T14:31:15ZengMDPI AGBiomedicines2227-90592023-11-011111303410.3390/biomedicines11113034Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture MethodsKrishan Gopal Jain0Nan Miles Xi1Runzhen Zhao2Waqas Ahmad3Gibran Ali4Hong-Long Ji5Department of Surgery, Health Sciences Division, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Mathematics and Statistics, Loyola University Chicago, Chicago, IL 60660, USADepartment of Surgery, Health Sciences Division, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADepartment of Surgery, Health Sciences Division, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USADivision of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN 55905, USADepartment of Surgery, Health Sciences Division, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USALung diseases rank third in terms of mortality and represent a significant economic burden globally. Scientists have been conducting research to better understand respiratory diseases and find treatments for them. An ideal in vitro model must mimic the in vivo organ structure, physiology, and pathology. Organoids are self-organizing, three-dimensional (3D) structures originating from adult stem cells, embryonic lung bud progenitors, embryonic stem cells (ESCs), and induced pluripotent stem cells (iPSCs). These 3D organoid cultures may provide a platform for exploring tissue development, the regulatory mechanisms related to the repair of lung epithelia, pathophysiological and immunomodulatory responses to different respiratory conditions, and screening compounds for new drugs. To create 3D lung organoids in vitro, both co-culture and feeder-free methods have been used. However, there exists substantial heterogeneity in the organoid culture methods, including the sources of AT2 cells, media composition, and feeder cell origins. This article highlights the currently available methods for growing AT2 organoids and prospective improvements to improve the available culture techniques/conditions. Further, we discuss various applications, particularly those aimed at modeling human distal lung diseases and cell therapy.https://www.mdpi.com/2227-9059/11/11/3034organoidsalveolar type 2 cellsstem cells3D culturespulmonary diseases
spellingShingle Krishan Gopal Jain
Nan Miles Xi
Runzhen Zhao
Waqas Ahmad
Gibran Ali
Hong-Long Ji
Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
Biomedicines
organoids
alveolar type 2 cells
stem cells
3D cultures
pulmonary diseases
title Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
title_full Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
title_fullStr Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
title_full_unstemmed Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
title_short Alveolar Type 2 Epithelial Cell Organoids: Focus on Culture Methods
title_sort alveolar type 2 epithelial cell organoids focus on culture methods
topic organoids
alveolar type 2 cells
stem cells
3D cultures
pulmonary diseases
url https://www.mdpi.com/2227-9059/11/11/3034
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AT nanmilesxi alveolartype2epithelialcellorganoidsfocusonculturemethods
AT runzhenzhao alveolartype2epithelialcellorganoidsfocusonculturemethods
AT waqasahmad alveolartype2epithelialcellorganoidsfocusonculturemethods
AT gibranali alveolartype2epithelialcellorganoidsfocusonculturemethods
AT honglongji alveolartype2epithelialcellorganoidsfocusonculturemethods