Skip to main content
News Schorle 12.2021
Embryoid after self-organization: - The pluripotent embryonic stem cells of a mouse are colored green, in the cells colored red the placental program is active and in the cells colored gray the membrane program is active.
© Jan Langkabel / Uni Bonn

News categories: Publication

Stem cells organize themselves to form embryoid

New insights into stem cell development in mice could enable an alternative to animal experiments in the future

Researchers of ImmunoSensation2 in cooperation with an international team have developed a method to generate embryo-like cell complexes from the stem cells of mice. The method provides new insights into embryonic development. In the medium term, it might also be suitable for developing tests for substances that could be harmful to fertility. The study has recently been published in Nature Communications.

It is still not fully understood how entire organisms develop from one single cell. Every type of tissue in the organism, whether it is bone, skin, muscle or the brain, is derived from one fertilized oocyte. This omnipotent cell subsequently develops into the blastocyst, which is implanted into the uterus, where it develops into an embryo. "Embryo development is largely based on self-organization," explains Prof. Dr. Hubert Schorle of the Institute of Pathology at the University of Bonn. "Each cell releases messenger substances into its environment and thereby helps determine the fate of its neighbors." The current study allows new insights into these precisely coordinated processes.

In vitro, three different stem cell lineages may be derived from the blastocyst and propagated in cell culture indefinitely: Trophoblast stem cells (TSCs), embryonic stem cells (ESCs) and extraembryonic endoderm (XEN) stem cells. The researchers around Prof. Schorle succeeded in maturing ESCs from mice into a so-called embryoid. Unlike the omnipotent oocyte, ESCs are pluripotent cells, exhibiting already restricted developmental abilities. "In addition to the actual embryo, the membrane that surrounds it and parts of the placenta also emerge from the egg," Schorle explains. "ESCs, on the other hand, cannot form these tissue structures outside the embryo."

However, ESCs play a decisive role in embryonic development: If ES cells are stimulated to divide, they merely turn into an undifferentiated cluster of cells. "We have now genetically modified some of the ES cells in our study," explains Schorle's colleague Jan Langkabel. He performed the main experiments in the study together with Arik Horne from Cluster Member Prof. Dr. Joachim Schultze's research group at the German Center for Neurodegenerative Diseases (DZNE) and the LIMES Institute at the University of Bonn. "Some ES cells were then able to form the membrane and others the embryonic portion of the placenta."

When the researchers brought these two modified cell lines together with the original ES cells, they observed something astonishing: The mouse cells differentiated in a finely balanced manner, eventually producing an embryo-like complex - an embryoid. "This resembled a 5-day-old mouse embryo," Arik Horne says. "The disordered mixture of the three cell types had therefore evolved into a strictly ordered structure, much like the one that normally emerges from a fertilized egg." Studies of their gene activity confirmed this finding: Each individual cell of the embryoid behaved very similarly to its counterpart in a real embryo.

Embryoids could help replace animal testing

It was already possible to create such embryoids before. However, this required the use of three completely different cell lines, which were grown separately in a strictly coordinated manner. This approach is very complex and error-prone - unlike the new method: "We work with a single culture," stresses Prof. Schorle, who, like Prof. Schultze, is a member of the Transdisciplinary Research Area (TRA) "Life and Health" at the University of Bonn. "We then switch on the placenta program after a certain time in one part of the cells and the membrane program in another part. The rest then happens, as it were, by itself through self-organization."

Prof. Schorle is now planning to create such embryoids from ES cells of monkeys in a very similar way. These could then be used for toxicity tests, he says - for example, to determine whether certain substances cause malformations in the womb. Toxicity studies like this currently still rely on animal testing. "The use of such embryoids could replace at least some of these," notes the researcher. He is already planning a corresponding cooperation project with researchers at the University of Göttingen.


Funding

The study was funded by the German Research Foundation (DFG).

Publication

Jan Langkabel et. al. (2021), Induction of Rosette-to-Lumen stage embryoids using reprogramming paradigms in ESCs; Nature Communications, DOI: 10.1038/s41467-021-27586-w


Contact

Prof. Dr. Joachim Schultze

German Center for Neurodegenerative Diseases (DZNE)

& the LIMES Institute at the University of Bonn

Phone +49 228/43302410

Email: Joachim.Schultze@dzne.de

Related news

News Icon

News categories: Publication

Malaria Causes Permanent Damage to Phagocytes in the Spleen

Macrophages formed in the bone marrow can only assume the function of embryonal phagocytes, or “scavenger cells,” to a certain degree according to a study by the University of Bonn and the Peter Doherty Institute for Infection and Immunity at the University of Melbourne. The researchers have demonstrated that malaria infection causes permanent damage to resident CD163 macrophages in the spleen, which are responsible for cleaning the blood, recycling iron and communicating with other cells involved in the body’s immune response.
View entry
Tracking glioblastoma cell spread in human brain tissue

News categories: Publication

Core2Edge: How tumor cells conquer the brain

Glioblastoma is an aggressive brain tumor that infiltrates deep into the surrounding brain tissue. Even after surgery, tumor cells remain in the brain and the tumor recurs. Bonn researchers have now developed Core2Edge, a model based entirely on human tissue that captures these hard-to-access infiltration zones at the tumor margin. The model enables investigation of the invasive front and direct assessment of new drug candidates in human tissue - without the need for animal testing. The study of the Brain Tumor Translational Research Group has now been published in Nature Protocols.
View entry
Mikrochip zur Wiederherstellung zentralen Sehvermögens bei fortgeschrittener Makuladegeneration.

News categories: Publication

Approval of a Novel Retinal Implant Technology

A novel retinal implant is offering people with geographic atrophy the opportunity to regain part of their central vision for the first time. Geographic atrophy is a severe late stage of age-related macular degeneration. An international research team led by Prof. Frank G. Holz of the UKB and the University of Bonn demonstrated in an international clinical trial that the majority of participants experienced significant improvements in visual acuity. The novel retinal implant technology has now received approval for routine clinical use in Europe, making it available beyond clinical trials.
View entry

Back to the news overview