Author
Listed:
- Laertis Ikonomou
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Michael J. Herriges
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Sara L. Lewandowski
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Robert Marsland
(Boston University)
- Carlos Villacorta-Martin
(Boston University and Boston Medical Center)
- Ignacio S. Caballero
(Boston University and Boston Medical Center)
- David B. Frank
(The Children’s Hospital of Philadelphia)
- Reeti M. Sanghrajka
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Keri Dame
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Maciej M. Kańduła
(Boston University
Boku University)
- Julia Hicks-Berthet
(Boston University School of Medicine)
- Matthew L. Lawton
(Boston University and Boston Medical Center
Boston University School of Medicine)
- Constantina Christodoulou
(Boston University School of Medicine)
- Attila J. Fabian
(Biogen Inc.)
- Eric Kolaczyk
(Boston University)
- Xaralabos Varelas
(Boston University School of Medicine)
- Edward E. Morrisey
(University of Pennsylvania)
- John M. Shannon
(Division of Pulmonary Biology, Cincinnati Children’s Hospital)
- Pankaj Mehta
(Boston University)
- Darrell N. Kotton
(Boston University and Boston Medical Center
Boston University School of Medicine)
Abstract
Multipotent Nkx2-1-positive lung epithelial primordial progenitors of the foregut endoderm are thought to be the developmental precursors to all adult lung epithelial lineages. However, little is known about the global transcriptomic programs or gene networks that regulate these gateway progenitors in vivo. Here we use bulk RNA-sequencing to describe the unique genetic program of in vivo murine lung primordial progenitors and computationally identify signaling pathways, such as Wnt and Tgf-β superfamily pathways, that are involved in their cell-fate determination from pre-specified embryonic foregut. We integrate this information in computational models to generate in vitro engineered lung primordial progenitors from mouse pluripotent stem cells, improving the fidelity of the resulting cells through unbiased, easy-to-interpret similarity scores and modulation of cell culture conditions, including substratum elastic modulus and extracellular matrix composition. The methodology proposed here can have wide applicability to the in vitro derivation of bona fide tissue progenitors of all germ layers.
Suggested Citation
Laertis Ikonomou & Michael J. Herriges & Sara L. Lewandowski & Robert Marsland & Carlos Villacorta-Martin & Ignacio S. Caballero & David B. Frank & Reeti M. Sanghrajka & Keri Dame & Maciej M. Kańduła , 2020.
"The in vivo genetic program of murine primordial lung epithelial progenitors,"
Nature Communications, Nature, vol. 11(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14348-3
DOI: 10.1038/s41467-020-14348-3
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Citations
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Cited by:
- Andrea B. Alber & Hector A. Marquez & Liang Ma & George Kwong & Bibek R. Thapa & Carlos Villacorta-Martin & Jonathan Lindstrom-Vautrin & Pushpinder Bawa & Feiya Wang & Yongfeng Luo & Laertis Ikonomou , 2023.
"Directed differentiation of mouse pluripotent stem cells into functional lung-specific mesenchyme,"
Nature Communications, Nature, vol. 14(1), pages 1-18, December.
- Ryan J. Geusz & Allen Wang & Dieter K. Lam & Nicholas K. Vinckier & Konstantinos-Dionysios Alysandratos & David A. Roberts & Jinzhao Wang & Samy Kefalopoulou & Araceli Ramirez & Yunjiang Qiu & Joshua , 2021.
"Sequence logic at enhancers governs a dual mechanism of endodermal organ fate induction by FOXA pioneer factors,"
Nature Communications, Nature, vol. 12(1), pages 1-19, December.
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