Inducible Stem-Cell-Derived Embryos Capture Mouse Morphogenetic Events In Vitro
Abstract
The development of mouse embryos can be partially recapitulated by combining embryonic stem cells (ESCs), trophoblast stem cells (TS), and extra-embryonic endoderm (XEN) stem cells to generate embryo-like structures called ETX embryos. Although ETX embryos transcriptionally capture the mouse gastrula, their ability to recapitulate complex morphogenic events such as gastrulation is limited, possibly due to the limited potential of XEN cells. To address this, we generated ESCs transiently expressing transcription factor Gata4, which drives the extra-embryonic endoderm fate, and combined them with ESCs and TS cells to generate induced ETX embryos (iETX embryos). We show that iETX embryos establish a robust anterior signaling center that migrates unilaterally to break embryo symmetry. Furthermore, iETX embryos gastrulate generating embryonic and extra-embryonic mesoderm and definitive endoderm. Our findings reveal that replacement of XEN cells with ESCs transiently expressing Gata4 endows iETX embryos with greater developmental potential, thus enabling the study of the establishment of anterior-posterior patterning and gastrulation in an in vitro system.
Additional Information
© 2020 The Authors. Under a Creative Commons license - Attribution 4.0 International (CC BY 4.0) Received 26 May 2020, Revised 26 October 2020, Accepted 4 December 2020, Available online 29 December 2020. We thank Marta Shahbazi, Neophytos Christodoulou, and David Glover for their advice and the members of the MZG laboratory for their feedback and encouragement. This work was supported by a European Research Council Grant (RG77946), Wellcome Trust (207415/Z/17/Z), Open Philanthropy, Shurl and Kay Curci, and Weston Havens Foundations grants awarded to M.Z.G.; K.Y.C.L. is supported by the Croucher Foundation and Cambridge Trust. F.H. is supported by a European Research Council Grant (695669) and Wellcome Trust (WT108438/C/15/Z). J.D.J. is supported by the Biotechnology and Biological Sciences Research Council. Author contributions. G.A. conceived the study and performed the work with the help of K.Y.C.L., C.W.G., C.C., and B.S. J.D.J. performed the single-cell sequencing analysis. F.H. supervised the single-cell sequencing analysis. M.Z. performed the chimera experiments. C.K. contributed to the live imaging. The study was supervised by M.Z.G. G.A. and M.Z.G. wrote the paper, with the help of K.Y.C.L., C.W.G., and J.D.J. The authors declare no competing interests.Attached Files
Published - 1-s2.0-S1534580720309795-main.pdf
Supplemental Material - 1-s2.0-S1534580720309795-mmc1.pdf
Supplemental Material - 1-s2.0-S1534580720309795-mmc2.mp4
Supplemental Material - 1-s2.0-S1534580720309795-mmc3.mp4
Supplemental Material - 1-s2.0-S1534580720309795-mmc4.mp4
Supplemental Material - 1-s2.0-S1534580720309795-mmc5.mp4
Supplemental Material - 1-s2.0-S1534580720309795-mmc6.mp4
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Additional details
- PMCID
- PMC7883308
- Eprint ID
- 107313
- Resolver ID
- CaltechAUTHORS:20210104-164232285
- European Research Council (ERC)
- RG77946
- Wellcome Trust
- 207415/Z/17/Z
- Open Philanthropy
- Shurl and Kay Curci Foundation
- Weston Havens Foundation
- Croucher Foundation
- Cambridge Trust
- European Research Council (ERC)
- 695669
- Wellcome Trust
- WT108438/C/15/Z
- Biotechnology and Biological Sciences Research Council (BBSRC)
- Created
-
2021-01-05Created from EPrint's datestamp field
- Updated
-
2023-07-21Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)