Regeneration of the alveolar epithelium is necessary to restore tissue architecture and gas exchange capabilities in chronic pulmonary diseases such as fibrosing interstitial lung disease. While it is known alveolar type 2 (AT2) cells give rise to alveolar type 1 (AT1) cells to repair the alveolar epithelium after injury, methods to promote this process under pathological settings are poorly understood. Here, using a complex 3D organoid culture with TGF-β1 dependent impaired AT1 spheroid formation, we performed a high-throughput screen (HTS) with ~16,800 compounds to identify small molecules that increase number of AT1 spheroids. Longitudinal single cell RNA sequencing (scRNA-seq) revealed that DB-11-BE87 increased AT1 regeneration by reducing TGF-β1 induced fibroblast activation, concurrently with AHR activation in those cells. These studies highlight a HTS system to identify factors that can promote AT1 differentiation and suggest AHR activation as a method to counteract pathological TGF-β1 signaling in pulmonary disease.
Triggering AHR resolves TGF-β1 induced fibroblast activation and promotes AT1 cell regeneration in alveolar organoids.
触发 AHR 可消除 TGF-β1 诱导的成纤维细胞活化,并促进肺泡类器官中 AT1 细胞的再生
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作者:Hagan Andrew S, Williams Scott, Mathison Casey J N, Yan Shanshan, Nguyen Bao, Federe Glenn C, Kuzu Guray, Siefert Joseph C, Hampton Janice, Chichkov Victor, Whitney Barnes S, King Frederick J, Taylor Brandon L, Walker John R, Zhao Rui, Elliott Jimmy, Phillips Dean P, Fang Bin, Decker Rebekah S
| 期刊: | Communications Biology | 影响因子: | 5.100 |
| 时间: | 2025 | 起止号: | 2025 Jul 9; 8(1):1025 |
| doi: | 10.1038/s42003-025-08446-5 | 研究方向: | 细胞生物学 |
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