© 2022, The Author(s), under exclusive licence to Springer Nature B.V.Human lung organoids (hLOs) are useful for disease modelling and drug screening. However, a lack of immune cells in hLOs limits the recapitulation of in vivo cellular physiology. Here, we generated hLOs containing alveolar macrophage (AMφ)–like cells derived from pluripotent stem cells (PSC). To bridge hLOs with advanced human lung high-resolution X-ray computed tomography (CT), we acquired quantitative micro-CT images. Three hLO types were observed during differentiation. Among them, alveolar hLOs highly expressed not only lung epithelial cell markers but also AMφ-specific markers. Furthermore, CD68+ AMφ-like cells were spatially organized on the luminal epithelial surfa...
This is the author accepted manuscript. The final version is available from European Respiratory Soc...
Background Respiratory medicine has high barriers to new drug development, with fewer approved new t...
Summary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stabl...
Human respiratory disease research currently lacks in vitro models that recapitulate most of the phy...
Stem cell technologies, especially patient-specific, induced stem cell pluripotency and directed dif...
Pulmonary fibrosis develops as a consequence of failed regeneration after injury. Analyzing mechanis...
Author ManuscriptRecapitulation of lung development from human pluripotent stem cells (hPSCs) in thr...
Repeated injury of the lung epithelium is proposed to be the main driver of idiopathic pulmonary fib...
Alveolar organoids (AOs), derived from human pluripotent stem cells (hPSCs) exhibit lung-specific fu...
Diseases such as idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, and bronchopu...
For RNAscope in situ hybridization, 8-µm FFPE tissue sections from HPS and IPF patients were incubat...
The lack of physiologically relevant in vitro models has hampered progress in understanding human lu...
Idiopathic pulmonary fibrosis (IPF) is characterized by alveolar epithelial cell injury, type II ce...
Stem cell technologies, especially patient-specific, induced stem cell pluripotency and directed dif...
Purpose: Idiopathic pulmonary fibrosis (IPF) is a complex progressive chronic lung disease where epi...
This is the author accepted manuscript. The final version is available from European Respiratory Soc...
Background Respiratory medicine has high barriers to new drug development, with fewer approved new t...
Summary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stabl...
Human respiratory disease research currently lacks in vitro models that recapitulate most of the phy...
Stem cell technologies, especially patient-specific, induced stem cell pluripotency and directed dif...
Pulmonary fibrosis develops as a consequence of failed regeneration after injury. Analyzing mechanis...
Author ManuscriptRecapitulation of lung development from human pluripotent stem cells (hPSCs) in thr...
Repeated injury of the lung epithelium is proposed to be the main driver of idiopathic pulmonary fib...
Alveolar organoids (AOs), derived from human pluripotent stem cells (hPSCs) exhibit lung-specific fu...
Diseases such as idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, and bronchopu...
For RNAscope in situ hybridization, 8-µm FFPE tissue sections from HPS and IPF patients were incubat...
The lack of physiologically relevant in vitro models has hampered progress in understanding human lu...
Idiopathic pulmonary fibrosis (IPF) is characterized by alveolar epithelial cell injury, type II ce...
Stem cell technologies, especially patient-specific, induced stem cell pluripotency and directed dif...
Purpose: Idiopathic pulmonary fibrosis (IPF) is a complex progressive chronic lung disease where epi...
This is the author accepted manuscript. The final version is available from European Respiratory Soc...
Background Respiratory medicine has high barriers to new drug development, with fewer approved new t...
Summary: It has been challenging to generate in vitro models of alveolar lung diseases, as the stabl...