A proposed model of a clock that governs the length of human pregnancy.
Todd RosenBingbing WangPublished in: Reproduction (Cambridge, England) (2024)
The mechanisms that govern the length of human pregnancy have not been determined, while preterm birth remains the leading cause of death and disability in newborns worldwide. Here, we review recent data to generate a novel hypothesis about how the pregnancy clock may function to initiate human labor in uncomplicated pregnancies. In this model, placental stress induced by the growing fetus drives placental production of NFKB, which is then activated by exosomes containing platelet-activating factor and complement 4-binding protein-A from the mature fetus, to drive pro-labor genes in the placenta. A better understanding of the clock that triggers labor may lead to new, more effective therapies to prevent spontaneous preterm birth.
Keyphrases
- preterm birth
- low birth weight
- gestational age
- endothelial cells
- induced pluripotent stem cells
- binding protein
- stem cells
- pluripotent stem cells
- multiple sclerosis
- mesenchymal stem cells
- pregnant women
- pregnancy outcomes
- genome wide
- gene expression
- electronic health record
- transcription factor
- stress induced
- cord blood
- urinary tract infection