Affiliations 

  • 1 Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
  • 2 Advanced Medical and Dental Institute, Universiti Sains Malaysia, Penang, Malaysia
  • 3 Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, United States
  • 4 Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, United States
Elife, 2022 01 12;11.
PMID: 35018887 DOI: 10.7554/eLife.67872

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.