Alveolar epithelial-like cell differentiation in a dynamic bioreactor: a promising 3D-approach for the high-throughput generation of lung cell types from human induced pluripotent stem cells.

IF 2.4
In vitro models Pub Date : 2023-06-29 eCollection Date: 2023-12-01 DOI:10.1007/s44164-023-00052-1
Michelle Müller, Yvonne Kohl, Anja Germann, Sylvia Wagner, Heiko Zimmermann, Hagen von Briesen
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Abstract

Purpose: Human induced pluripotent stem cell (hiPSC)-derived lung cell types such as alveolar epithelial cells are promising for toxicological and pharmaceutical in vitro screenings. Reproducible differentiation processes are highly demanded, but protocols which are suitable for the high-throughput generation of lung cell types from hiPSCs are lacking.

Methods: In this study, a new approach for the hiPSC-differentiation in alveolar epithelial-like cells type 2 under dynamic 3D-conditions in a suspension bioreactor is presented. Gene and protein expression analyses of key markers during the embryonal lung development have been performed in comparison to cells differentiated under static 2D-conditions to evaluate the differentiation efficacy of the new bioreactor-based approach. Finally, the resulting cells were infected by SARS-CoV-2 pseudotypes to demonstrate their functionality and suitability for e.g. COVID-19 drug development.

Results: The dynamic bioreactor is suitable to differentiate hiPSCs in spheroids, which express relevant lung markers in each developmental stage on gene and protein level. The 3D method is able to significantly increase the expression of some markers in comparison to conventional 2D differentiation. 3D-differentiated alveolar epithelial-like cells express functional SARS-CoV-2 receptors and can display the viral infection.

Conclusion: The presented dynamic 3D-differentiation is a promising, new approach to generate alveolar epithelial-like cells from hiPSCs as cell source for in vitro lung models.

Supplementary information: The online version contains supplementary material available at 10.1007/s44164-023-00052-1.

动态生物反应器中的肺泡上皮样细胞分化:从人诱导多能干细胞中高通量生成肺细胞类型的有前途的3d方法。
目的:人诱导多能干细胞(hiPSC)衍生的肺细胞类型,如肺泡上皮细胞,在体外毒理学和药物筛选方面有前景。可重复的分化过程是高度需要的,但适合从hipsc高通量生成肺细胞类型的方案缺乏。方法:本研究提出了一种在悬浮生物反应器中动态3d条件下诱导肺泡上皮样细胞2型hipsc分化的新方法。我们对胚胎肺发育过程中关键标志物的基因和蛋白表达进行了分析,并与静态2d条件下分化的细胞进行了比较,以评估基于生物反应器的新方法的分化效果。最后,用SARS-CoV-2伪病毒感染生成的细胞,以证明其功能和适用性,例如用于COVID-19药物开发。结果:动态生物反应器适合分化hiPSCs为球体,在基因和蛋白水平上表达各发育阶段肺相关标志物。与传统的2D分化相比,3D方法能够显著增加某些标记物的表达。3d分化肺泡上皮样细胞表达功能性SARS-CoV-2受体,并能显示病毒感染。结论:动态3d分化是一种很有前途的新方法,可以从hipsc中获得肺泡上皮样细胞作为体外肺模型的细胞来源。补充资料:在线版本提供补充资料,网址为10.1007/s44164-023-00052-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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