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Generation of induced alveolar assembloids with functional alveolar-like macrophages
  • Kang, Ji Su ;
  • Lee, Youngsun ;
  • Gil, Dayeon ;
  • Kim, Min Jung ;
  • Wood, Connor ;
  • Delorme, Vincent ;
  • Lee, Jeong Mi ;
  • Ko, Kyong Cheol ;
  • Kim, Jung Hyun ;
  • Lee, Mi Ok
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dc.contributor.authorKang, Ji Su-
dc.contributor.authorLee, Youngsun-
dc.contributor.authorGil, Dayeon-
dc.contributor.authorKim, Min Jung-
dc.contributor.authorWood, Connor-
dc.contributor.authorDelorme, Vincent-
dc.contributor.authorLee, Jeong Mi-
dc.contributor.authorKo, Kyong Cheol-
dc.contributor.authorKim, Jung Hyun-
dc.contributor.authorLee, Mi Ok-
dc.date.issued2025-12-01-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://aurora.ajou.ac.kr/handle/2018.oak/38258-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105002984438&origin=inward-
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.description.sponsorshipThis research was supported by grants from the National Research Foundation of Korea (2022M3A9J1072296, RS-2023-00225239, 2021R1C1C1006725, RS-2024-00458236) funded by the Ministry of Science, ICT and Future Planning, Korea Centers for Disease Control and Prevention (2020ER610100, 2023-NS-001-00) and the Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program (KGM4722533, KGM5362521). The funders had no role in the study design, data collection or analysis, decision to publish, or preparation of the manuscript. The authors acknowledge the facilities, and the scientific and technical assistance of the EM & Histology Core Facility and Dr. Yongsuk Hur at the BioMedical Research Center, Korea Advanced Institute of Science and Technology. Additionally, ChatGPT(OpenAI, San Francisco, CA, USA) assisted with sentence editing.-
dc.language.isoeng-
dc.publisherNature Research-
dc.subject.meshAlveolar Epithelial Cells-
dc.subject.meshCell Differentiation-
dc.subject.meshCoculture Techniques-
dc.subject.meshGranulocyte-Macrophage Colony-Stimulating Factor-
dc.subject.meshHumans-
dc.subject.meshInduced Pluripotent Stem Cells-
dc.subject.meshInterleukin-1beta-
dc.subject.meshInterleukin-6-
dc.subject.meshLung-
dc.subject.meshMacrophages, Alveolar-
dc.subject.meshMycobacterium tuberculosis-
dc.subject.meshOrganoids-
dc.subject.meshPulmonary Alveoli-
dc.titleGeneration of induced alveolar assembloids with functional alveolar-like macrophages-
dc.typeArticle-
dc.citation.number1-
dc.citation.titleNature Communications-
dc.citation.volume16-
dc.identifier.bibliographicCitationNature Communications, Vol.16 No.1-
dc.identifier.doi10.1038/s41467-025-58450-w-
dc.identifier.pmid40199883-
dc.identifier.scopusid2-s2.0-105002984438-
dc.identifier.urlhttps://www.nature.com/ncomms/-
dc.type.otherArticle-
dc.identifier.pissn20411723-
dc.subject.subareaChemistry (all)-
dc.subject.subareaBiochemistry, Genetics and Molecular Biology (all)-
dc.subject.subareaPhysics and Astronomy (all)-
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