Extravillous trophoblast cell derived exosomes induce vascular smooth muscle cell apoptosis via a mechanism associated with miR-143-3p

The remodeling of uterine spiral arteries is a complex process requiring the dynamic action of various cell types. During early pregnancy, extravillous trophoblast cells (EVT) differentiate and invade the vascular wall, replacing the vascular smooth muscle cells (VSMCs). Several in vitro studies have shown that EVT cells play an important role in promoting VSMC Apoptosis, however the mechanism underlying this process is not fully understood. In this study, we demonstrated that EVT conditioned media and EVT-derived exosomes could induce VSMC Apoptosis. Through data mining and experimental verification, it was demonstrated that the EVT exosome miR-143-3p induced VSMC Apoptosis in both VSMCs and a chorionic plate artery (CPA) model. Furthermore, FAS ligand was also expressed on the EVT-exosomes and may play a coordinated role in Apoptosis induction. These data clearly demonstrated that VSMC Apoptosis is mediated by EVT-derived exosomes and their cargo of miR-143-3p as well as their cell surface presentation of FASL. This finding increases our understanding of the molecular mechanisms underlying the regulation of VSMC Apoptosis during spiral artery remodeling.

Extravillous trophoblast cell; FASL; apoptosis; exosome; miR-143-3p; pregnancy; spiral artery remodeling; vascular smooth muscle cell.