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具有功能性肺泡样巨噬细胞的诱导性肺泡类器官的生成。

Generation of induced alveolar assembloids with functional alveolar-like macrophages.

作者信息

Kang Ji Su, Lee Youngsun, Lee Youngsun, Gil Dayeon, Kim Min Jung, Wood Connor, Delorme Vincent, Lee Jeong Mi, Ko Kyong-Cheol, Kim Jung-Hyun, Lee Mi-Ok

机构信息

Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.

KRIBB School of Bioscience, University of Science and Technology (UST), Daejeon, 34113, Republic of Korea.

出版信息

Nat Commun. 2025 Apr 9;16(1):3346. doi: 10.1038/s41467-025-58450-w.

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.

摘要

在人类肺脏中,肺泡上皮细胞与驻留巨噬细胞之间的相互作用在健康和疾病状态下均塑造着肺的发育和功能。为了研究这些过程,我们开发了一种共培养系统,该系统将人类多能干细胞衍生的肺泡上皮类器官与诱导的巨噬细胞相结合,以创建一个功能性环境,称为诱导肺泡组装体。通过单细胞RNA测序和功能分析,我们鉴定出产生粒细胞-巨噬细胞集落刺激因子(GM-CSF)的2型肺泡样细胞,其支持巨噬细胞的组织适应性;以及分泌白细胞介素-1β和白细胞介素-6、表达表面活性剂代谢基因并展示核心免疫功能的巨噬细胞样细胞。响应肺泡上皮损伤时,巨噬细胞样细胞可有效清除受损细胞并吸收氧化脂质。暴露于细菌成分或感染结核分枝杆菌表明,这些组装体重现了人类呼吸道防御的关键方面。这些发现突出了诱导肺泡组装体作为研究人类肺发育、免疫和疾病的平台的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac97/11978882/f2a6c0554d18/41467_2025_58450_Fig1_HTML.jpg

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