| Literature DB >> 35018887 |
Wai Hoe Ng1, Elizabeth K Johnston1, Jun Jie Tan2, Jacqueline M Bliley1,3, Adam W Feinberg1,3, Donna B Stolz4, Ming Sun4, Piyumi Wijesekara1, Finn Hawkins5, Darrell N Kotton5, Xi Ren1.
Abstract
The extensive crosstalk between the developing heart and lung is critical to their proper morphogenesis and maturation. However, there remains a lack of models that investigate the critical cardio-pulmonary mutual interaction during human embryogenesis. Here, we reported a novel stepwise strategy for directing the simultaneous induction of both mesoderm-derived cardiac and endoderm-derived lung epithelial lineages within a single differentiation of human-induced pluripotent stem cells (hiPSCs) via temporal specific tuning of WNT and nodal signaling in the absence of exogenous growth factors. Using 3D suspension culture, we established concentric cardio-pulmonary micro-Tissues (μTs), and expedited alveolar maturation in the presence of cardiac accompaniment. Upon withdrawal of WNT agonist, the cardiac and pulmonary components within each dual-lineage μT effectively segregated from each other with concurrent initiation of cardiac contraction. We expect that our multilineage differentiation model will offer an experimentally tractable system for investigating human cardio-pulmonary interaction and tissue boundary formation during embryogenesis.Entities:
Keywords: alveolar maturation; cardio-pulmonary co-differentiation; developmental biology; human; pluripotent stem cell; regenerative medicine; stem cells; tissue segregation
Mesh:
Year: 2022 PMID: 35018887 PMCID: PMC8846595 DOI: 10.7554/eLife.67872
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140