Generation of induced alveolar assembloids with functional alveolar-like macrophages

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dc.contributor.authorJi Su Kang-
dc.contributor.authorY Lee-
dc.contributor.authorYoungsun Lee-
dc.contributor.authorD Gil-
dc.contributor.authorM J Kim-
dc.contributor.authorC Wood-
dc.contributor.authorV Delorme-
dc.contributor.authorJeong Mi Lee-
dc.contributor.authorKyong-Cheol Ko-
dc.contributor.authorJ H Kim-
dc.contributor.authorMi Ok Lee-
dc.date.accessioned2025-04-10T16:32:24Z-
dc.date.available2025-04-10T16:32:24Z-
dc.date.issued2025-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/37673-
dc.description.abstractWithin 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.-
dc.publisherSpringer-Nature Pub Group-
dc.titleGeneration of induced alveolar assembloids with functional alveolar-like macrophages-
dc.title.alternativeGeneration of induced alveolar assembloids with functional alveolar-like macrophages-
dc.typeArticle-
dc.citation.titleNature Communications-
dc.citation.number0-
dc.citation.endPage3346-
dc.citation.startPage3346-
dc.citation.volume16-
dc.contributor.affiliatedAuthorJi Su Kang-
dc.contributor.affiliatedAuthorYoungsun Lee-
dc.contributor.affiliatedAuthorJeong Mi Lee-
dc.contributor.affiliatedAuthorKyong-Cheol Ko-
dc.contributor.affiliatedAuthorMi Ok Lee-
dc.contributor.alternativeName강지수-
dc.contributor.alternativeName이영선-
dc.contributor.alternativeName이영선-
dc.contributor.alternativeName길다연-
dc.contributor.alternativeName김민정-
dc.contributor.alternativeNameWood-
dc.contributor.alternativeNameDelorme-
dc.contributor.alternativeName이정미-
dc.contributor.alternativeName고경철-
dc.contributor.alternativeName김정현-
dc.contributor.alternativeName이미옥-
dc.identifier.bibliographicCitationNature Communications, vol. 16, pp. 3346-3346-
dc.identifier.doi10.1038/s41467-025-58450-w-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > Korea Preclinical Evaluation Center > 1. Journal Articles
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
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