Skip Navigation

Publication Detail

Title: Bisphenol S Impairs Invasion and Proliferation of Extravillous Trophoblasts Cells by Interfering with Epidermal Growth Factor Receptor Signaling.

Authors: Ticiani, Elvis; Pu, Yong; Gingrich, Jeremy; Veiga-Lopez, Almudena

Published In Int J Mol Sci, (2022 Jan 08)

Abstract: The placenta supports fetal growth and is vulnerable to exogenous chemical exposures. We have previously demonstrated that exposure to the emerging chemical bisphenol S (BPS) can alter placental endocrine function. Mechanistically, we have demonstrated that BPS interferes with epidermal growth factor receptor (EGFR) signaling, reducing placenta cell fusion. Extravillous trophoblasts (EVTs), a placenta cell type that aids with vascular remodeling, require EGF to invade into the maternal endometrium. We hypothesized that BPS would impair EGF-mediated invasion and proliferation in EVTs. Using human EVTs (HTR-8/SVneo cells), we tested whether BPS could inhibit the EGF response by blocking EGFR activation. We also evaluated functional endpoints of EGFR signaling, including EGF endocytosis, cell invasion and proliferation, and endovascular differentiation. We demonstrated that BPS blocked EGF-induced phosphorylation of EGFR by acting as a competitive antagonist to EGFR. Transwell assay and a three-dimensional microfluidic chip invasion assay revealed that BPS exposure can block EGF-mediated cell invasion. BPS also blocked EGF-mediated proliferation and endovascular differentiation. In conclusion, BPS can prevent EGF-mediated EVT proliferation and invasion through EGFR antagonism. Given the role of EGFR in trophoblast proliferation and differentiation during placental development, our findings suggest that maternal exposure to BPS may contribute to placental dysfunction via EGFR-mediated mechanisms.

PubMed ID: 35054855 Exiting the NIEHS site

MeSH Terms: Cell Differentiation/drug effects; Cell Line; Cell Proliferation/drug effects; Collagen/pharmacology; Drug Combinations; Endocytosis/drug effects; Epidermal Growth Factor/pharmacology; ErbB Receptors/metabolism*; Humans; Laminin/pharmacology; Neovascularization, Physiologic/drug effects; Phenols/toxicity*; Phosphorylation/drug effects; Proteoglycans/pharmacology; Signal Transduction*/drug effects; Sulfones/toxicity*; Trophoblasts/drug effects; Trophoblasts/pathology*

Back
to Top