In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids

Summary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stable culture of alveolar type 2 (AT2) cells has been difficult. Methods of generating and expanding AT2 cells derived from induced pluripotent stem cells (iPSCs) have been established and are expected to...

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Main Authors: Yohei Korogi, Shimpei Gotoh, Satoshi Ikeo, Yuki Yamamoto, Naoyuki Sone, Koji Tamai, Satoshi Konishi, Tadao Nagasaki, Hisako Matsumoto, Isao Ito, Toyofumi F. Chen-Yoshikawa, Hiroshi Date, Masatoshi Hagiwara, Isao Asaka, Akitsu Hotta, Michiaki Mishima, Toyohiro Hirai
Format: Article
Language:English
Published: Elsevier 2019-03-01
Series:Stem Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2213671119300165
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language English
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author Yohei Korogi
Shimpei Gotoh
Satoshi Ikeo
Yuki Yamamoto
Naoyuki Sone
Koji Tamai
Satoshi Konishi
Tadao Nagasaki
Hisako Matsumoto
Isao Ito
Toyofumi F. Chen-Yoshikawa
Hiroshi Date
Masatoshi Hagiwara
Isao Asaka
Akitsu Hotta
Michiaki Mishima
Toyohiro Hirai
spellingShingle Yohei Korogi
Shimpei Gotoh
Satoshi Ikeo
Yuki Yamamoto
Naoyuki Sone
Koji Tamai
Satoshi Konishi
Tadao Nagasaki
Hisako Matsumoto
Isao Ito
Toyofumi F. Chen-Yoshikawa
Hiroshi Date
Masatoshi Hagiwara
Isao Asaka
Akitsu Hotta
Michiaki Mishima
Toyohiro Hirai
In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
Stem Cell Reports
author_facet Yohei Korogi
Shimpei Gotoh
Satoshi Ikeo
Yuki Yamamoto
Naoyuki Sone
Koji Tamai
Satoshi Konishi
Tadao Nagasaki
Hisako Matsumoto
Isao Ito
Toyofumi F. Chen-Yoshikawa
Hiroshi Date
Masatoshi Hagiwara
Isao Asaka
Akitsu Hotta
Michiaki Mishima
Toyohiro Hirai
author_sort Yohei Korogi
title In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
title_short In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
title_full In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
title_fullStr In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
title_full_unstemmed In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar Organoids
title_sort in vitro disease modeling of hermansky-pudlak syndrome type 2 using human induced pluripotent stem cell-derived alveolar organoids
publisher Elsevier
series Stem Cell Reports
issn 2213-6711
publishDate 2019-03-01
description Summary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stable culture of alveolar type 2 (AT2) cells has been difficult. Methods of generating and expanding AT2 cells derived from induced pluripotent stem cells (iPSCs) have been established and are expected to be applicable to disease modeling. Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder characterized by dysfunction of lysosome-related organelles, such as lamellar bodies (LBs), in AT2 cells. From an HPS type 2 (HPS2) patient, we established disease-specific iPSCs (HPS2-iPSCs) and their gene-corrected counterparts. By live cell imaging, the LB dynamics were visualized and altered distribution, enlargement, and impaired secretion of LBs were demonstrated in HPS2-iPSC-derived AT2 cells. These findings provide insight into the AT2 dysfunction in HPS patients and support the potential use of human iPSC-derived AT2 cells for future research on alveolar lung diseases. : Pulmonary surfactant secretion by alveolar type 2 (AT2) cells is crucial for alveolar homeostasis. Gotoh and colleagues generated Hermansky-Pudlak syndrome type 2 (HPS2) patient-derived iPSCs and their gene-corrected counterparts and differentiated them into alveolar organoids (AOs). In HPS2-AOs, aberrant lamellar bodies and impaired surfactant secretion were demonstrated. Human iPSC-derived AOs might be useful for investigating alveolar lung diseases. Keywords: iPSC, Hermansky-Pudlak syndrome, HPS, lamellar body, alveolar type 2 cell, pulmonary surfactant, pluripotent stem cell, pulmonary fibrosis, alveolar organoid, MX35
url http://www.sciencedirect.com/science/article/pii/S2213671119300165
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spelling doaj-ed2685dbfb1944db8b6cdca4a1e13b212020-11-25T01:02:30ZengElsevierStem Cell Reports2213-67112019-03-01123431440In Vitro Disease Modeling of Hermansky-Pudlak Syndrome Type 2 Using Human Induced Pluripotent Stem Cell-Derived Alveolar OrganoidsYohei Korogi0Shimpei Gotoh1Satoshi Ikeo2Yuki Yamamoto3Naoyuki Sone4Koji Tamai5Satoshi Konishi6Tadao Nagasaki7Hisako Matsumoto8Isao Ito9Toyofumi F. Chen-Yoshikawa10Hiroshi Date11Masatoshi Hagiwara12Isao Asaka13Akitsu Hotta14Michiaki Mishima15Toyohiro Hirai16Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan; Department of Drug Discovery for Lung Diseases, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan; Corresponding authorDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Anatomy and Developmental Biology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, JapanDepartment of Fundamental Cell Technology, Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, JapanDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanSummary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stable culture of alveolar type 2 (AT2) cells has been difficult. Methods of generating and expanding AT2 cells derived from induced pluripotent stem cells (iPSCs) have been established and are expected to be applicable to disease modeling. Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder characterized by dysfunction of lysosome-related organelles, such as lamellar bodies (LBs), in AT2 cells. From an HPS type 2 (HPS2) patient, we established disease-specific iPSCs (HPS2-iPSCs) and their gene-corrected counterparts. By live cell imaging, the LB dynamics were visualized and altered distribution, enlargement, and impaired secretion of LBs were demonstrated in HPS2-iPSC-derived AT2 cells. These findings provide insight into the AT2 dysfunction in HPS patients and support the potential use of human iPSC-derived AT2 cells for future research on alveolar lung diseases. : Pulmonary surfactant secretion by alveolar type 2 (AT2) cells is crucial for alveolar homeostasis. Gotoh and colleagues generated Hermansky-Pudlak syndrome type 2 (HPS2) patient-derived iPSCs and their gene-corrected counterparts and differentiated them into alveolar organoids (AOs). In HPS2-AOs, aberrant lamellar bodies and impaired surfactant secretion were demonstrated. Human iPSC-derived AOs might be useful for investigating alveolar lung diseases. Keywords: iPSC, Hermansky-Pudlak syndrome, HPS, lamellar body, alveolar type 2 cell, pulmonary surfactant, pluripotent stem cell, pulmonary fibrosis, alveolar organoid, MX35http://www.sciencedirect.com/science/article/pii/S2213671119300165