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Human alveolar progenitors generate dual lineage bronchioalveolar organoids

Authors

  • K. Hoffmann
  • B. Obermayer
  • K. Hönzke
  • D. Fatykhova
  • Z. Demir
  • A. Löwa
  • L.G. Teixeira-Alves
  • E. Wyler
  • E. Lopez-Rodriguez
  • M. Mieth
  • M. Baumgardt
  • J. Hoppe
  • T.C. Firsching
  • M. Tönnies
  • T.T. Bauer
  • S. Eggeling
  • H.L. Tran
  • P. Schneider
  • J. Neudecker
  • J.C. Rückert
  • A.D. Gruber
  • M. Ochs
  • M. Landthaler
  • D. Beule
  • N. Suttorp
  • S. Hippenstiel
  • A.C. Hocke
  • M. Kessler

Journal

  • Communications Biology

Citation

  • Commun Biol 5 (1): 875

Abstract

  • Mechanisms of epithelial renewal in the alveolar compartment remain incompletely understood. To this end, we aimed to characterize alveolar progenitors. Single-cell RNA-sequencing (scRNA-seq) analysis of the HTII-280(+)/EpCAM(+) population from adult human lung revealed subclusters enriched for adult stem cell signature (ASCS) genes. We found that alveolar progenitors in organoid culture in vitro show phenotypic lineage plasticity as they can yield alveolar or bronchial cell-type progeny. The direction of the differentiation is dependent on the presence of the GSK-3β inhibitor, CHIR99021. By RNA-seq profiling of GSK-3β knockdown organoids we identified additional candidate target genes of the inhibitor, among others FOXM1 and EGF. This gives evidence of Wnt pathway independent regulatory mechanisms of alveolar specification. Following influenza A virus (IAV) infection organoids showed a similar response as lung tissue explants which confirms their suitability for studies of sequelae of pathogen-host interaction.


DOI

doi:10.1038/s42003-022-03828-5