If the development of blood vessels in the placenta is impaired, fetal growth retardation may result. Scientists from the German Cancer Research Center (DKFZ) and the Mannheim Medical Faculty of Heidelberg University discovered that the correct development of functioning blood vessels in the mouse placenta is controlled epigenetically: One of the enzymes that modify gene activity using methyl groups is responsible. The researchers also observed a connection with a deficiency of this “methyltransferase” in a well-known pregnancy complication.
In all female mammals, including humans, the growing fetus in the uterus is supplied via the placenta. Through this temporary organ, the fetus is connected to the mother's bloodstream, receiving nutrients and oxygen and releasing waste products.
In the case of placental insufficiency, the placenta is not supplied with a sufficient amount of blood and the exchange of substances between the placenta and fetus does not function properly. This endangers the supply of the fetus. As a rule, a developmental disorder of the blood vessels of the placenta is responsible for this.
Vascular specialist Hellmut Augustin from the DKFZ and the Mannheim Medical Faculty of Heidelberg University is well aware of the enormous importance of blood vessel development during pregnancy: “Abnormal growth of the placental blood vessels is the main cause of fetal growth retardation.” In order to gain a better understanding of how such malformations can arise, Augustin and his team have now examined the blood vessels of the mouse placenta at the single-cell level.
The researchers focused on the endothelial cells that line the inside of the blood vessels and play a crucial role in the formation of new blood vessels. Their focus was on the endothelial cells from the area of the mouse placenta that corresponds to the chorionic villi in humans.
The team found that in the normally formed placenta, the activity of certain critical genes in the endothelial cells decreases from the maternal to the fetal side. This zonation occurs in relation to the strength of the blood flow. What is the reason for this? Epigenetic mechanisms such as DNA methylation are responsible for stronger or weaker gene expression in the cell. Therefore, the researchers analyzed the enzymes responsible for DNA methylation, the so-called DNA methyltransferases. In doing so, DNA methyltransferase DNMT3A turned out to be mainly responsible for the methylation of the fetal placental endothelium.
When DNMT3A was genetically switched off in the endothelial cells of the mice, DNA methylation decreased and the spatial zonation of endothelial gene expression was lost. The development of the placental vasculature, which is crucial for the fetus, was impaired. This resulted in retarded growth, which was still noticeable after birth.
To find out whether these results obtained in mice correlate with findings in pregnant women, Augustin's team scoured the gene databases: They compared previously published single-cell RNA sequence data from endothelial cells in healthy placentas with placentas from women suffering from preeclampsia. This complication can cause growth disorders in the baby because it is no longer properly supplied via the placenta. As expected based on the results obtained in the mouse, the placental endothelium of the preeclampsia patients had reduced DNMT3A expression.
“The combination of the compelling mouse data with the correlative patient data suggests that DNMT3A plays a crucial role in the healthy development of placental vessels – and that a deficiency of this enzyme could contribute significantly to the development of placental insufficiency,” explains Stephanie Gehrs, the first author of the publication. “A better understanding of the underlying mechanisms leading to placental insufficiency forms the basis for future approaches to better understand pregnancy disorders and possibly treat them in a more targeted manner.”
Stephanie Gehrs, Moritz Jakab, Ewgenija Gutjahr, Zuguang Gu; Dieter Wiechenhahn, Jan-Philipp Mallm, Carolin Mogler, Matthias Schlesner, Christoph Plass, Katarina Schlereth, Hellmut G. Augustin: The spatial zonation of the placental vasculature is specified by epigenetic mechanisms.
Dev. Cell 2025, https://doi.org/10.1016/j.devcel.2024.12.037
With more than 3,000 employees, the German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ) is Germany’s largest biomedical research institute. DKFZ scientists identify cancer risk factors, investigate how cancer progresses and develop new cancer prevention strategies. They are also developing new methods to diagnose tumors more precisely and treat cancer patients more successfully. The DKFZ's Cancer Information Service (KID) provides patients, interested citizens and experts with individual answers to questions relating to cancer.
To transfer promising approaches from cancer research to the clinic and thus improve the prognosis of cancer patients, the DKFZ cooperates with excellent research institutions and university hospitals throughout Germany:
National Center for Tumor Diseases (NCT, 6 sites)
German Cancer Consortium (DKTK, 8 sites)
Hopp Children's Cancer Center (KiTZ) Heidelberg
Helmholtz Institute for Translational Oncology (HI-TRON Mainz) - A Helmholtz Institute of the DKFZ
DKFZ-Hector Cancer Institute at the University Medical Center Mannheim
National Cancer Prevention Center (jointly with German Cancer Aid)
The DKFZ is 90 percent financed by the Federal Ministry of Education and Research and 10 percent by the state of Baden-Württemberg. The DKFZ is a member of the Helmholtz Association of German Research Centers.
Journal
Developmental Cell