In vitro generation of human pluripotent stem cell derived lung organoids

Author:

Dye Briana R1,Hill David R2,Ferguson Michael AH2,Tsai Yu-Hwai2,Nagy Melinda S2,Dyal Rachel2,Wells James M34,Mayhew Christopher N3,Nattiv Roy5,Klein Ophir D567,White Eric S2,Deutsch Gail H8,Spence Jason R129

Affiliation:

1. Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, United States

2. Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, United States

3. Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, United States

4. Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, United States

5. Institute for Human Genetics, Department of Pediatrics, University of California, San Francisco, San Francisco, United States

6. Program in Craniofacial and Mesenchymal Biology, University of California, San Francisco, San Francisco, United States

7. Center for Craniofacial Anomalies, University of California, San Francisco, San Francisco, United States

8. Department of Laboratories, Seattle Children's Hospital and University of Washington, Seattle, United States

9. Center for Organogenesis, University of Michigan Medical School, Ann Arbor, United States

Abstract

Recent breakthroughs in 3-dimensional (3D) organoid cultures for many organ systems have led to new physiologically complex in vitro models to study human development and disease. Here, we report the step-wise differentiation of human pluripotent stem cells (hPSCs) (embryonic and induced) into lung organoids. By manipulating developmental signaling pathways hPSCs generate ventral-anterior foregut spheroids, which are then expanded into human lung organoids (HLOs). HLOs consist of epithelial and mesenchymal compartments of the lung, organized with structural features similar to the native lung. HLOs possess upper airway-like epithelium with basal cells and immature ciliated cells surrounded by smooth muscle and myofibroblasts as well as an alveolar-like domain with appropriate cell types. Using RNA-sequencing, we show that HLOs are remarkably similar to human fetal lung based on global transcriptional profiles, suggesting that HLOs are an excellent model to study human lung development, maturation and disease.

Funder

National Heart, Lung, and Blood Institute (NHBLI)

March of Dimes Foundation

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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