A recent study in the Journal of Lipid Research sheds some light on a new facet of progesterone signaling between maternal and embryonic tissue, and hints at a preliminary link between disruptions to this signaling and recurrent miscarriage.
Progesterone plays an important role in embedding the placenta into the endometrium, the lining of the uterus. The hormone is key for thickening the endometrium, reorganizing blood flow to supply the uterus with oxygen and nutrients, and suppressing the maternal immune system.
Progesterone is made in the ovary as a normal part of the menstrual cycle, and at first, this continues after fertilization. About six weeks into pregnancy, the placenta takes over making progesterone, a critical handoff. (The placenta also makes other hormones, including human chorionic gonadotropin, which is detected in a pregnancy test.) Placental progesterone comes mostly from surface tissue organized into fingerlike projections that integrate into the endometrium and absorb nutrients. Some cells leave those projections and migrate into the endometrium, where they help to direct the reorganization of arteries.
Austrian researchers led by Sigrid Vondra and supervised by Jürgen Pollheimer and Clemens Röhrl compared the cells that stay on the placenta’s surface with those that migrate into the endometrium. They discovered that the enzymes responsible for progesterone production differ between the two cell types early in pregnancy.
As a steroid hormone, progesterone is derived from cholesterol. Although the overall production of progesterone appears to be about the same in migratory and surface cells of the placenta, migratory cells accumulate more cholesterol and express more of a key enzyme for converting cholesterol to progesterone. Among women who have had recurrent miscarriages, that enzyme is lower in migratory cells from the placenta compared to women with healthy pregnancies. In contrast, levels of the enzyme don’t differ between healthy and miscarried pregnancies in cells from the surface of the placenta.
The team’s findings suggest that production of progesterone by the migratory cells may have a specific and necessary role in early pregnancy and that disruption to that process could be linked to miscarriage.
“If we can identify the exact mechanisms and cells which are affected,” Vondra said, “that would lead us one step closer to understanding the big picture of what causes recurrent miscarriages and possibly to being able to intervene and allow these women to have successful pregnancies.”
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Doi: 10.1194/jlr.P093427
This research was supported by the Austrian Science Fund (Grants P25763-B13 and P31470-B30) and Austrian National Bank (Grant 17613). Other authors who contributed to the study include Victoria Kunihs, Tanja Eberhart, Karin Eigner, Raimund Bauer, Peter Haslinger, Sandra Haider, Karin Windsperger, Gunter Klambauer, Birgit Schutz, Mario Mikula, Xiaowei Zhu, Alexander Urban, Roberta Hannibal, Julie Baker, Martin Knofler and Herbert Stangl.
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