Recapitulating human cardio-pulmonary co-development using simultaneous multilineage differentiation of pluripotent stem cells

  1. Wai Hoe Ng
  2. Elizabeth K Johnston
  3. Jun Jie Tan
  4. Jacqueline M Bliley
  5. Adam W Feinberg
  6. Donna B Stolz
  7. Ming Sun
  8. Piyumi Wijesekara
  9. Finn Hawkins
  10. Darrell N Kotton
  11. Xi Ren  Is a corresponding author
  1. Carnegie Mellon University, United States
  2. Universiti Sains Malaysia, Malaysia
  3. University of Pittsburgh, United States
  4. Boston University, United States

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 (mTs), and expedited alveolar maturation in the presence of cardiac accompaniment. Upon withdrawal of WNT agonist, the cardiac and pulmonary components within each dual-lineage mT 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.

Data availability

All data supporting the findings of this study are available within the article and its supplementary files. Source data files have been provided for Figures 1 to 6.

Article and author information

Author details

  1. Wai Hoe Ng

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    Competing interests
    Wai Hoe Ng, is a co-inventor of a related provisional patent application (No. 63/124422) entitled 'Methods for simultaneous cardio-pulmonary differentiation and alveolar maturation from human pluripotent stem cells'..
  2. Elizabeth K Johnston

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    Competing interests
    Elizabeth K Johnston, is a co-inventor of a related provisional patent application (No. 63/124422) entitled 'Methods for simultaneous cardio-pulmonary differentiation and alveolar maturation from human pluripotent stem cells'..
  3. Jun Jie Tan

    Advanced Medical and Dental Institute, Universiti Sains Malaysia, Penang, Malaysia
    Competing interests
    No competing interests declared.
  4. Jacqueline M Bliley

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    Competing interests
    No competing interests declared.
  5. Adam W Feinberg

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    Competing interests
    No competing interests declared.
  6. Donna B Stolz

    Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, United States
    Competing interests
    No competing interests declared.
  7. Ming Sun

    Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, United States
    Competing interests
    No competing interests declared.
  8. Piyumi Wijesekara

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    Competing interests
    No competing interests declared.
  9. Finn Hawkins

    Center for Regenerative Medicine, Boston University, Boston, United States
    Competing interests
    No competing interests declared.
  10. Darrell N Kotton

    Center for Regenerative Medicine, Boston University, Boston, MA, United States
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9604-8476
  11. Xi Ren

    Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, United States
    For correspondence
    xiren@cmu.edu
    Competing interests
    Xi Ren, is a co-inventor of a related provisional patent application (No. 63/124422) entitled 'Methods for simultaneous cardio-pulmonary differentiation and alveolar maturation from human pluripotent stem cells'..
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3187-1311

Funding

Samuel & Emma Winters Foundation (A025662)

  • Xi Ren

Carnegie Mellon University

  • Xi Ren

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2022, Ng et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 2,769
    views
  • 455
    downloads
  • 23
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Wai Hoe Ng
  2. Elizabeth K Johnston
  3. Jun Jie Tan
  4. Jacqueline M Bliley
  5. Adam W Feinberg
  6. Donna B Stolz
  7. Ming Sun
  8. Piyumi Wijesekara
  9. Finn Hawkins
  10. Darrell N Kotton
  11. Xi Ren
(2022)
Recapitulating human cardio-pulmonary co-development using simultaneous multilineage differentiation of pluripotent stem cells
eLife 11:e67872.
https://doi.org/10.7554/eLife.67872

Share this article

https://doi.org/10.7554/eLife.67872

Further reading

    1. Developmental Biology
    Shannon H Carroll, Sogand Schafer ... Eric C Liao
    Research Article

    Wnt signaling plays crucial roles in embryonic patterning including the regulation of convergent extension (CE) during gastrulation, the establishment of the dorsal axis, and later, craniofacial morphogenesis. Further, Wnt signaling is a crucial regulator of craniofacial morphogenesis. The adapter proteins Dact1 and Dact2 modulate the Wnt signaling pathway through binding to Disheveled. However, the distinct relative functions of Dact1 and Dact2 during embryogenesis remain unclear. We found that dact1 and dact2 genes have dynamic spatiotemporal expression domains that are reciprocal to one another suggesting distinct functions during zebrafish embryogenesis. Both dact1 and dact2 contribute to axis extension, with compound mutants exhibiting a similar CE defect and craniofacial phenotype to the wnt11f2 mutant. Utilizing single-cell RNAseq and an established noncanonical Wnt pathway mutant with a shortened axis (gpc4), we identified dact1/2-specific roles during early development. Comparative whole transcriptome analysis between wildtype and gpc4 and wildtype and dact1/2 compound mutants revealed a novel role for dact1/2 in regulating the mRNA expression of the classical calpain capn8. Overexpression of capn8 phenocopies dact1/2 craniofacial dysmorphology. These results identify a previously unappreciated role of capn8 and calcium-dependent proteolysis during embryogenesis. Taken together, our findings highlight the distinct and overlapping roles of dact1 and dact2 in embryonic craniofacial development, providing new insights into the multifaceted regulation of Wnt signaling.

    1. Developmental Biology
    Dena Goldblatt, Basak Rosti ... David Schoppik
    Research Article

    Sensorimotor reflex circuits engage distinct neuronal subtypes, defined by precise connectivity, to transform sensation into compensatory behavior. Whether and how motor neuron populations specify the subtype fate and/or sensory connectivity of their pre-motor partners remains controversial. Here, we discovered that motor neurons are dispensable for proper connectivity in the vestibular reflex circuit that stabilizes gaze. We first measured activity following vestibular sensation in pre-motor projection neurons after constitutive loss of their extraocular motor neuron partners. We observed normal responses and topography indicative of unchanged functional connectivity between sensory neurons and projection neurons. Next, we show that projection neurons remain anatomically and molecularly poised to connect appropriately with their downstream partners. Lastly, we show that the transcriptional signatures that typify projection neurons develop independently of motor partners. Our findings comprehensively overturn a long-standing model: that connectivity in the circuit for gaze stabilization is retrogradely determined by motor partner-derived signals. By defining the contribution of motor neurons to specification of an archetypal sensorimotor circuit, our work speaks to comparable processes in the spinal cord and advances our understanding of principles of neural development.