Estrogen and Progesterone Receptors Are Dysregulated at the BPH/5 Mouse Preeclamptic-Like Maternal-Fetal Interface.
Viviane C L GomesBryce M GilbertCarolina BernalKassandra R CrissmanJennifer L SonesPublished in: Biology (2024)
The etiopathogenesis of preeclampsia, a leading hypertensive disorder of pregnancy, has been proposed to involve an abnormal circulating sex hormone profile and misexpression of placental estrogen and progesterone receptors (ER and PR, respectively). However, existing research is vastly confined to third trimester preeclamptic placentas. Consequently, the placental-uterine molecular crosstalk and the dynamic ER and PR expression pattern in the peri-conception period remain overlooked. Herein, our goal was to use the BPH/5 mouse to elucidate pre-pregnancy and early gestation Er and Pr dynamics in a preeclamptic-like uterus. BPH/5 females display low circulating estrogen concentration during proestrus, followed by early gestation hypoestrogenemia, hyperprogesteronemia, and a spontaneous preeclamptic-like phenotype. Preceding pregnancy, the gene encoding Er alpha (Erα, Esr1 ) is upregulated in the diestrual BPH/5 uterus. At the peak of decidualization, Esr1 , Er beta (Erβ, Esr2 ), and Pr isoform B ( Pr-B ) were upregulated in the BPH/5 maternal-fetal interface. At the protein level, BPH/5 females display higher percentage of decidual cells with nuclear Erα expression, as well as Pr downregulation in the decidua, luminal and glandular epithelium. In conclusion, we provide evidence of disrupted sex hormone signaling in the peri-conception period of preeclamptic-like pregnancies, potentially shedding some light onto the intricate role of sex hormone signaling at unexplored timepoints of human preeclampsia.
Keyphrases
- estrogen receptor
- pregnancy outcomes
- benign prostatic hyperplasia
- lower urinary tract symptoms
- preterm birth
- endoplasmic reticulum
- poor prognosis
- breast cancer cells
- endothelial cells
- blood pressure
- preterm infants
- induced apoptosis
- cell proliferation
- long non coding rna
- single molecule
- small molecule
- cell death
- transcription factor
- gene expression
- cell cycle arrest
- genome wide identification