[Development of human iPS cell-derived alveolar and airway models using micropatterning plate for SARS-CoV-2 research].

Uirusu Pub Date : 2024-01-01 DOI:10.2222/jsv.74.35
Rina Hashimoto, Atsushi Masui, Shimpei Gotoh, Kazuo Takayama
{"title":"[Development of human iPS cell-derived alveolar and airway models using micropatterning plate for SARS-CoV-2 research].","authors":"Rina Hashimoto, Atsushi Masui, Shimpei Gotoh, Kazuo Takayama","doi":"10.2222/jsv.74.35","DOIUrl":null,"url":null,"abstract":"<p><p>Advanced cell culture systems including human induced pluripotent stem (iPS) cells and organoids enable the generation of intricate structural and functional organ models in vitro. Application of these advanced cell culture systems to research on a wide range of diseases including infectious diseases is underway. Due to the impact of the coronavirus disease 2019 (COVID-19) pandemic, advanced cell culture systems in the virus research field are rapidly becoming popular. Respiratory models generated using human iPS cells and organoid technology are useful for analyzing respiratory cell responses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. However, there is still room for the development of an apical-out model, which is essential for simple virus infection experiments, and a model that can analyze host responses in the alveoli and airways. In this study, we developed human iPS cell-derived alveolar and airway models with an apical-out structure by using a micropatterning plate. In the alveolar model, we confirmed that this model contains abundant type II alveolar epithelial (AT2) cells, which are the target cells of SARS-CoV-2 in the alveoli. In the airway model, we confirmed that this model contains abundant ciliated cells, which are the target cells of SARS-CoV-2 in the airway. Using our alveolar and airway models, we can analyze the differences in infection efficiency and host response of each SARS-CoV-2 variant. We hope that the human iPS cell-derived alveolar and airway models generated using a micropatterning plate will be used to analyze not only SARS-CoV-2 but also a wide range of respiratory viruses.</p>","PeriodicalId":75275,"journal":{"name":"Uirusu","volume":"74 1","pages":"35-44"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Uirusu","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2222/jsv.74.35","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Advanced cell culture systems including human induced pluripotent stem (iPS) cells and organoids enable the generation of intricate structural and functional organ models in vitro. Application of these advanced cell culture systems to research on a wide range of diseases including infectious diseases is underway. Due to the impact of the coronavirus disease 2019 (COVID-19) pandemic, advanced cell culture systems in the virus research field are rapidly becoming popular. Respiratory models generated using human iPS cells and organoid technology are useful for analyzing respiratory cell responses caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. However, there is still room for the development of an apical-out model, which is essential for simple virus infection experiments, and a model that can analyze host responses in the alveoli and airways. In this study, we developed human iPS cell-derived alveolar and airway models with an apical-out structure by using a micropatterning plate. In the alveolar model, we confirmed that this model contains abundant type II alveolar epithelial (AT2) cells, which are the target cells of SARS-CoV-2 in the alveoli. In the airway model, we confirmed that this model contains abundant ciliated cells, which are the target cells of SARS-CoV-2 in the airway. Using our alveolar and airway models, we can analyze the differences in infection efficiency and host response of each SARS-CoV-2 variant. We hope that the human iPS cell-derived alveolar and airway models generated using a micropatterning plate will be used to analyze not only SARS-CoV-2 but also a wide range of respiratory viruses.

[利用微图板开发人类iPS细胞衍生的肺泡和气道模型用于SARS-CoV-2研究]。
包括人类诱导多能干细胞和类器官在内的先进细胞培养系统能够在体外生成复杂的结构和功能器官模型。这些先进的细胞培养系统正在应用于包括传染病在内的广泛疾病的研究中。由于2019冠状病毒病(COVID-19)大流行的影响,病毒研究领域的先进细胞培养系统迅速受到欢迎。利用人类iPS细胞和类器官技术生成的呼吸道模型可用于分析由严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染引起的呼吸道细胞反应。然而,对于简单的病毒感染实验和分析肺泡和气道中宿主反应的模型来说,仍有发展的空间。在这项研究中,我们利用微图板建立了人类iPS细胞衍生的具有尖向外结构的肺泡和气道模型。在肺泡模型中,我们证实该模型含有丰富的II型肺泡上皮细胞(AT2),这是SARS-CoV-2在肺泡中的靶细胞。在气道模型中,我们证实该模型含有丰富的纤毛细胞,纤毛细胞是SARS-CoV-2在气道中的靶细胞。利用我们的肺泡和气道模型,我们可以分析每种SARS-CoV-2变体的感染效率和宿主反应的差异。我们希望利用微图板生成的人类iPS细胞衍生的肺泡和气道模型不仅可以用于分析SARS-CoV-2,还可以用于分析各种呼吸道病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信