Modeling fibrotic alveolar transitional cells with pluripotent stem cell-derived alveolar organoids

• Published in: Life science alliance Vol. 6; no. 8; p. e202201853
• Main Authors: Ptasinski, Victoria, Monkley, Susan J, Öst, Karolina, Tammia, Markus, Alsafadi, Hani N, Overed-Sayer, Catherine, Hazon, Petra, Wagner, Darcy E, Murray, Lynne A
• Format: Journal Article
• Language: English
• Published: United States Life Science Alliance LLC 01.08.2023
• Subjects: Alveolar Epithelial Cells - metabolism; Basic Medicine; Cell and Molecular Biology; Cell- och molekylärbiologi; Clinical Medicine; Fibrosis; Humans; Idiopathic Pulmonary Fibrosis - metabolism; Klinisk medicin; Lung - metabolism; Lungmedicin och allergi; Medical and Health Sciences; Medicin och hälsovetenskap; Medicinska och farmaceutiska grundvetenskaper; Organoids - metabolism; Pluripotent Stem Cells - metabolism; Respiratory Medicine and Allergy
• ISSN: 2575-1077; 2575-1077
• DOI: 10.26508/lsa.202201853

Repeated injury of the lung epithelium is proposed to be the main driver of idiopathic pulmonary fibrosis (IPF). However, available therapies do not specifically target the epithelium and human models of fibrotic epithelial damage with suitability for drug discovery are lacking. We developed a model of the aberrant epithelial reprogramming observed in IPF using alveolar organoids derived from human-induced pluripotent stem cells stimulated with a cocktail of pro-fibrotic and inflammatory cytokines. Deconvolution of RNA-seq data of alveolar organoids indicated that the fibrosis cocktail rapidly increased the proportion of transitional cell types including the aberrant basaloid phenotype recently identified in the lungs of IPF patients. We found that epithelial reprogramming and extracellular matrix (ECM) production persisted after removal of the fibrosis cocktail. We evaluated the effect of the two clinically approved compounds for IPF, nintedanib and pirfenidone, and found that they reduced the expression of ECM and pro-fibrotic mediators but did not completely reverse epithelial reprogramming. Thus, our system recapitulates key aspects of IPF and is a promising system for drug discovery.