IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v16y2025i1d10.1038_s41467-025-58450-w.html
   My bibliography  Save this article

Generation of induced alveolar assembloids with functional alveolar-like macrophages

Author

Listed:
  • Ji Su Kang

    (Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    University of Science and Technology (UST))

  • Youngsun Lee

    (Korea National Institute of Health)

  • Youngsun Lee

    (Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    University of Science and Technology (UST))

  • Dayeon Gil

    (Korea National Institute of Health)

  • Min Jung Kim

    (Korea National Institute of Health)

  • Connor Wood

    (Institute Pasteur Korea)

  • Vincent Delorme

    (Institute Pasteur Korea)

  • Jeong Mi Lee

    (Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    University of Science and Technology (UST))

  • Kyong-Cheol Ko

    (Korea Research Institute of Bioscience and Biotechnology (KRIBB))

  • Jung-Hyun Kim

    (Korea National Institute of Health
    Ajou University
    Ajou University)

  • Mi-Ok Lee

    (Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    University of Science and Technology (UST))

Abstract

Within the human lung, interactions between alveolar epithelial cells and resident macrophages shape lung development and function in both health and disease. To study these processes, we develop a co-culture system combining human pluripotent stem cell-derived alveolar epithelial organoids and induced macrophages to create a functional environment, termed induced alveolar assembloids. Using single-cell RNA sequencing and functional analyses, we identify alveolar type 2-like cells producing GM-CSF, which supports macrophage tissue adaptation, and macrophage-like cells that secrete interleukin-1β and interleukin-6, express surfactant metabolism genes, and demonstrate core immune functions. In response to alveolar epithelial injury, macrophage-like cells efficiently eliminate damaged cells and absorb oxidized lipids. Exposure to bacterial components or infection with Mycobacterium tuberculosis reveals that these assembloids replicate key aspects of human respiratory defense. These findings highlight the potential of induced alveolar assembloids as a platform to investigate human lung development, immunity, and disease.

Suggested Citation

  • Ji Su Kang & Youngsun Lee & Youngsun Lee & Dayeon Gil & Min Jung Kim & Connor Wood & Vincent Delorme & Jeong Mi Lee & Kyong-Cheol Ko & Jung-Hyun Kim & Mi-Ok Lee, 2025. "Generation of induced alveolar assembloids with functional alveolar-like macrophages," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58450-w
    DOI: 10.1038/s41467-025-58450-w
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-025-58450-w
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-025-58450-w?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58450-w. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.