Sex-Specific Differences in the Placental Unfolded Protein Response in a Rodent Model of Gestational Hypoxia.
Wen TongEsha GangulyRoberto Villalobos-LabraAnita L QuonFloor SpaansDino A GiussaniSandra T DavidgePublished in: Reproductive sciences (Thousand Oaks, Calif.) (2022)
Gestational hypoxia is a major contributor to fetal growth restriction (FGR) and perinatal morbidity and mortality and has been closely linked to the activation of the unfolded protein response (UPR) in the placenta. Recent studies on adverse pregnancy conditions show differential adaptive responses in pregnancies carrying male or female fetuses. Here, we use an established rat model of hypoxic pregnancy and FGR to test the hypothesis that chronic hypoxia promotes sexually dimorphic activation of the placental UPR. Our data showed that gestational hypoxia increased glucose regulatory protein 78 (GRP78) expression in male placentae, increased activating transcription factor 6 activation (ATF6) in female placentae, and did not induce changes in other UPR markers. In addition, gestational hypoxia reduced fetal weight only in males and ATF6 activation correlated with an increase in the fetal crown-rump-length/body weight ratio only in females. These results suggest sex-specific divergence in the placental adaptive response to gestational hypoxia, which may account for the sexual dimorphism observed in placental function and pregnancy outcomes in complicated pregnancies.
Keyphrases
- pregnancy outcomes
- pregnant women
- weight gain
- transcription factor
- endothelial cells
- body weight
- endoplasmic reticulum stress
- preterm birth
- body mass index
- protein protein
- binding protein
- poor prognosis
- type diabetes
- amino acid
- physical activity
- mental health
- weight loss
- metabolic syndrome
- signaling pathway
- machine learning
- insulin resistance
- big data
- glycemic control