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
Novartis Biomedical Research, San Diego, CA, USA.
Pulmongene (Beijing) Ltd., Medical Technology Center, Beijing, China.
Commun Biol. 2025 Jul 9;8(1):1025. doi: 10.1038/s42003-025-08446-5.
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.
肺泡上皮的再生对于恢复诸如纤维化间质性肺病等慢性肺部疾病的组织结构和气体交换能力是必要的。虽然已知肺泡2型(AT2)细胞在损伤后会产生肺泡1型(AT1)细胞来修复肺泡上皮,但在病理情况下促进这一过程的方法却知之甚少。在这里,我们使用一种复杂的3D类器官培养体系,该体系中TGF-β1依赖性地损害AT1球体形成,我们用约16,800种化合物进行了高通量筛选(HTS),以鉴定能增加AT1球体数量的小分子。纵向单细胞RNA测序(scRNA-seq)显示,DB-11-BE87通过减少TGF-β1诱导的成纤维细胞活化来增加AT1再生,同时这些细胞中的芳烃受体(AHR)也被激活。这些研究突出了一种用于鉴定可促进AT1分化的因子的HTS系统,并表明AHR激活是一种对抗肺部疾病中病理性TGF-β1信号传导的方法。