诱导多能干细胞
基质凝胶
生物
内胚层
细胞生物学
肺
胚胎干细胞
干细胞
免疫学
病理
癌症研究
医学
血管生成
遗传学
内科学
基因
作者
Chen‐Yong Lin,Sarah X.L. Huang,Ana Luísa Rodrigues Toste de Carvalho,Siu‐Hong Ho,Mohammad Naimul Islam,Stefano Volpi,Luigi D. Notarangelo,Michael J. Ciancanelli,Jean‐Laurent Casanova,Jahar Bhattacharya,Feng Liang,Laura M. Palermo,Matteo Porotto,Anne Moscona,Hans‐Willem Snoeck
摘要
Chen et al. generate lung bud organoids from human pluripotent stem cells that recapitulate early lung development, such as branching airway formation and early alveolar structures, which could potentially be used to model lung disease. Recapitulation of lung development from human pluripotent stem cells (hPSCs) in three dimensions (3D) would allow deeper insight into human development, as well as the development of innovative strategies for disease modelling, drug discovery and regenerative medicine1. We report here the generation from hPSCs of lung bud organoids (LBOs) that contain mesoderm and pulmonary endoderm and develop into branching airway and early alveolar structures after xenotransplantation and in Matrigel 3D culture. Expression analysis and structural features indicated that the branching structures reached the second trimester of human gestation. Infection in vitro with respiratory syncytial virus, which causes small airway obstruction and bronchiolitis in infants2, led to swelling, detachment and shedding of infected cells into the organoid lumens, similar to what has been observed in human lungs3. Introduction of mutation in HPS1, which causes an early-onset form of intractable pulmonary fibrosis4,5, led to accumulation of extracellular matrix and mesenchymal cells, suggesting the potential use of this model to recapitulate fibrotic lung disease in vitro. LBOs therefore recapitulate lung development and may provide a useful tool to model lung disease.
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