Tuesday, July 25, 2023

 

Researchers generate human embryo-like structures that include extraembryonic tissue


Peer-Reviewed Publication

CELL PRESS

Peri-gastruloid with an embryonic disc-like structure CREDIT Cell Liu et al. 

VIDEO: PERI-GASTRULOID WITH AN EMBRYONIC DISC-LIKE STRUCTURE CREDIT CELL LIU ET AL. view more 

CREDIT: CELL LIU ET AL.




Gastrulation, the process where an embryo reorganizes itself from a hollow sphere into a multilayered structure, is considered a “black box” of human development. This is because human embryos are typically not cultured for longer than 14 days because of bioethical concerns, and gastrulation occurs between 17- and 21-days post-fertilization. In addition, current stem cell models that mimic gastrulation have not been able to include the necessary extraembryonic tissues that give rise to the yolk sac and the placenta. In a study appearing on July 20 in the journal Cell, researchers report a new method to develop “peri-gastruloids,” an embryo-like structure that includes one of the supporting tissues, the yolk sac, missing from previous models.

“While non-integrated models of human gastrulation and early organogenesis have been developed from primed human pluripotent stem cells, these models lack the extraembryonic cells that play vital roles in embryo patterning and morphogenesis,” says senior author Jun Wu, a stem cell biologist at the University of Texas Southwestern Medical Center. “The presence of both embryonic and extraembryonic tissues enables researchers to examine the interactions between the epiblast, amnion, and yolk sac during gastrulation—an endeavor previously unattainable in humans.”

Instead of the more commonly used primed pluripotent stem cells, the researchers’ method used expanded pluripotent stem cells (EPSCs). These cells have previously been shown to differentiate into both embryonic and extraembryonic tissue in mice. By adding the proper growth factors to human EPSCs, they differentiated into these two types of tissues. The cells then self-organized into structures that resembled the human embryo, which the researchers refer to as “peri-gastruloids.”

Extraembryonic tissues release chemical signals that guide embryo development, which allows these peri-gastruloids to mimic several important processes that are considered part of this black-box period of development. Peri-gastruloids develop the amniotic cavity that embryos live inside, and the yolk sac cavities that provide the embryos with blood supply. In addition, peri-gastruloids show early signs of organogenesis, such as neurulation, which marks the very beginning of central nervous system development.

The research team reports that their method is efficient and reproducible. In what they consider a small-scale trial, they were able to generate hundreds of peri-gastruloids. “The power of this model stems from its ability to exploit the remarkable self-organizing capacity of human EPSCs with minimal external intervention” says Wu. 

The team notes that peri-gastruloids are not viable because of the exclusion of trophoblasts that give rise to the placenta, which helps assuage the ethical concerns of this research. This project followed international stem cell research guidelines and was approved by UT Southwestern’s Stem Cell Oversight Committee.

Time-lapse showing cell migrat [VIDEO] | 


3D Rendering of a Peri-Gastrul [VIDEO] | 


This work was supported by the New York Stem Cell Foundation and the American Society for Reproductive Medicine Research Institute. More information about conflicts of interests can be found in the paper.

Cell, Liu et al. “Modeling post-implantation stages of human development into early organogenesis with stem cell-derived peri-gastruloids” https://cell.com/cell/fulltext/S0092-8674(23)00794-8


Cell (@CellCellPress)the flagship journal of Cell Press, is a bimonthly journal that publishes findings of unusual significance in any area of experimental biology, including but not limited to cell biology, molecular biology, neuroscience, immunology, virology and microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. Visit: http://www.cell.com/cell. To receive Cell Press media alerts, contact press@cell.com.

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