Functional human iPSC-derived alveolar-like cells cultured in a miniaturized 96‑Transwell air–liquid interface model

In order to circumvent the limited access and donor variability of human primary alveolar cells, directed differentiation of human pluripotent stem cells (hiPSCs) into alveolar-like cells, provides a promising tool for respiratory disease modeling and drug discovery assays. In this work, a unique, m...

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Bibliographic Details
Published in:Scientific reports 2021-08, Vol.11 (1), p.1-19, Article 17028
Main Authors: Bluhmki, Teresa, Traub, Stefanie, Müller, Ann-Kathrin, Bitzer, Sarah, Schruf, Eva, Bammert, Marie-Therese, Leist, Marcel, Gantner, Florian, Garnett, James P, Heilker, Ralf
Format: Article
Language:English
Subjects:
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Alveoli
Cell differentiation
Cytokines
Cytology
Drug discovery
Epithelium
Growth factors
Humanities and Social Sciences
mRNA
multidisciplinary
Phenotypes
Pluripotency
Progenitor cells
Respiratory diseases
Science
Science (multidisciplinary)
Stem cells
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Summary:In order to circumvent the limited access and donor variability of human primary alveolar cells, directed differentiation of human pluripotent stem cells (hiPSCs) into alveolar-like cells, provides a promising tool for respiratory disease modeling and drug discovery assays. In this work, a unique, miniaturized 96-Transwell microplate system is described where hiPSC-derived alveolar-like cells were cultured at an air–liquid interface (ALI). To this end, hiPSCs were differentiated into lung epithelial progenitor cells (LPCs) and subsequently matured into a functional alveolar type 2 (AT2)-like epithelium with monolayer-like morphology. AT2-like cells cultured at the physiological ALI conditions displayed characteristics of AT2 cells with classical alveolar surfactant protein expressions and lamellar-body like structures. The integrity of the epithelial barriers between the AT2-like cells was confirmed by applying a custom-made device for 96-parallelized transepithelial electric resistance (TEER) measurements. In order to generate an IPF disease-like phenotype in vitro, the functional AT2-like cells were stimulated with cytokines and growth factors present in the alveolar tissue of IPF patients. The cytokines stimulated the secretion of pro-fibrotic biomarker proteins both on the mRNA (messenger ribonucleic acid) and protein level. Thus, the hiPSC-derived and cellular model system enables the recapitulation of certain IPF hallmarks, while paving the route towards a miniaturized medium throughput approach of pharmaceutical drug discovery.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-96565-4