EconPapers    
Economics at your fingertips  
 

Precardiac organoids form two heart fields via Bmp/Wnt signaling

Peter Andersen (), Emmanouil Tampakakis, Dennisse V. Jimenez, Suraj Kannan, Matthew Miyamoto, Hye Kyung Shin, Amir Saberi, Sean Murphy, Edrick Sulistio, Stephen P. Chelko and Chulan Kwon ()
Additional contact information
Peter Andersen: Johns Hopkins University School of Medicine
Emmanouil Tampakakis: Johns Hopkins University School of Medicine
Dennisse V. Jimenez: Johns Hopkins University School of Medicine
Suraj Kannan: Johns Hopkins University School of Medicine
Matthew Miyamoto: Johns Hopkins University School of Medicine
Hye Kyung Shin: Johns Hopkins University School of Medicine
Amir Saberi: Johns Hopkins University School of Medicine
Sean Murphy: Johns Hopkins University School of Medicine
Edrick Sulistio: Johns Hopkins University School of Medicine
Stephen P. Chelko: Johns Hopkins University School of Medicine
Chulan Kwon: Johns Hopkins University School of Medicine

Nature Communications, 2018, vol. 9, issue 1, 1-13

Abstract: Abstract The discovery of the first heart field (FHF) and the second heart field (SHF) led us to understand how cardiac lineages and structures arise during development. However, it remains unknown how they are specified. Here, we generate precardiac spheroids with pluripotent stem cells (PSCs) harboring GFP/RFP reporters under the control of FHF/SHF markers, respectively. GFP+ cells and RFP+ cells appear from two distinct areas and develop in a complementary fashion. Transcriptome analysis shows a high degree of similarities with embryonic FHF/SHF cells. Bmp and Wnt are among the most differentially regulated pathways, and gain- and loss-of-function studies reveal that Bmp specifies GFP+ cells and RFP+ cells via the Bmp/Smad pathway and Wnt signaling, respectively. FHF/SHF cells can be isolated without reporters by the surface protein Cxcr4. This study provides novel insights into understanding the specification of two cardiac origins, which can be leveraged for PSC-based modeling of heart field/chamber-specific disease.

Date: 2018
References: Add references at CitEc
Citations: View citations in EconPapers (1)

Downloads: (external link)
https://www.nature.com/articles/s41467-018-05604-8 Abstract (text/html)

Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.

Export reference: BibTeX RIS (EndNote, ProCite, RefMan) HTML/Text

Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05604-8

Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/

DOI: 10.1038/s41467-018-05604-8

Access Statistics for this article

Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie

More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().

 
Page updated 2025-03-19
Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05604-8