Protocol for the differentiation of human alveolar epithelial type I cells from pluripotent stem cell-derived type II-like cells

Pulmonary alveolar epithelial type I (AT1) cells have a flattened morphology to permit the diffusion of oxygen into the capillaries and historically have been difficult to isolate or maintain in culture. Here, we present a protocol for generating human alveolar type I-like cells (induced pluripotent stem cell-derived AT1s [iAT1s]) from induced pluripotent stem cell-derived alveolar epithelial type II cells (iAT2s) in vitro. We describe steps to plate iAT1s in either 3D or air-liquid interface cultures and to analyze or isolate iAT1s via flow cytometry. For complete details on the use and execution of this protocol, please refer to Burgess et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2025-03-01
DOI
https://doi.org/10.1016/j.xpro.2025.103667
Citations
2
Primary Topic
Neonatal Respiratory Health Research
Type
article
Field-Weighted Citation Impact
3.04
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article

Protocol for the differentiation of human alveolar epithelial type I cells from pluripotent stem cell-derived type II-like cells

Kasey Minakin, Claire L. Burgess, Darrell N. Kotton, Konstantinos–Dionysios Alysandratos et al.
2 citations
STAR Protocols
Neonatal Respiratory Health Research
3.04
article

Protocol for the differentiation of human alveolar epithelial type I cells from pluripotent stem cell-derived type II-like cells

Kasey Minakin, Claire L. Burgess, Darrell N. Kotton, Konstantinos–Dionysios Alysandratos, Xaralabos Varelas, Lauren J. Ayers
article en
2 citations

Abstract

Pulmonary alveolar epithelial type I (AT1) cells have a flattened morphology to permit the diffusion of oxygen into the capillaries and historically have been difficult to isolate or maintain in culture. Here, we present a protocol for generating human alveolar type I-like cells (induced pluripotent stem cell-derived AT1s [iAT1s]) from induced pluripotent stem cell-derived alveolar epithelial type II cells (iAT2s) in vitro. We describe steps to plate iAT1s in either 3D or air-liquid interface cultures and to analyze or isolate iAT1s via flow cytometry. For complete details on the use and execution of this protocol, please refer to Burgess et al.<sup>1</sup>.

STAR ProtocolsVol. 6(1)
Boston University (US), Boston Medical Center (US)
Zero hunger
Openalex Percentile: Top 11%
Neonatal Respiratory Health Research
3.04
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Protocol for the differentiation of human alveolar epithelial type I cells from pluripotent stem cell-derived type II-like cells — Kasey Minakin, Claire L. Burgess, et al. · STAR Protocols (2025) | TGRS Research Map | TGRS