Poster Presentation The Annual Scientific Meeting of the Endocrine Society of Australia and the Society for Reproductive Biology 2014

The effects of ethanol on trophoblast tell differentiation in culture (#216)

Jacinta I Kalisch-Smith 1 , Sarah E Steane 1 , Marie Pantaleon 1 , Karen M Moritz 1 , David G Simmons 1
  1. School of Biomedical Science, University of Queensland, Brisbane, QLD, Australia

Alcohol consumption is widespread among pregnant women in Australia, particularly prior to pregnancy recognition. We have recently shown in an in vivo rodent model of peri-conceptional ethanol [EtOH] exposure, that early exposure results in sex-specific changes to placental morphology in late gestation. Since the EtOH exposure occurs prior to implantation, we hypothesised that EtOH may directly alter the differentiation of trophoblast stem (TS) cells, derived from the trophectoderm, and the allocation of placental lineages, important for the formation of the definitive placenta.

In the current study, male mouse TS cells (RS26) were differentiated for 6 days in the presence of 0% (control), 0.2%, or 1% EtOH (n=3/treatment), and assayed for the expression of lineage-restricted trophoblast subtype markers. RNA was extracted for q-PCR and the expression of genes specific to the labyrinth (Ctsq, Syna, Slc16a1, Slc16a3) and junctional zones (Tpbpa, Prl7a2, Prl7b1, Prl2c1, Prl3d1) were analysed.

EtOH treatment caused reductions in the expression of Syna (syncytiotrophoblast layer 1 [SynT-I], P<0.05), Prl7b1 (spiral-artery associated trophoblast giant cells [SpA-TGCs] and glycogen cells [GlyT], P<0.05), and Prl7a2 (spongiotrophoblast [SpT] cells, P<0.001). No alterations were found for the remaining markers.

The observed reductions in gene expression suggest EtOH exposure can either delay TS cell differentiation or alter cell allocation to specific lineages. A reduction in the differentiation of labyrinthine cells (SynT-I) in vivo would lead to a reduced surface area for nutrient transport, while a reduction in the differentiation of junctional zone-derived subtypes (SpA-TGC, SpT, GlyT) would decrease trophoblast invasion and/or endocrine activity. Perturbations in all of these trophoblast subtypes have previously been implicated in foetal growth restriction. 

We have shown that direct EtOH exposure results in alterations to placental cell types present within differentiating male TS cell cultures. Future analysis of female TS cells will determine if these changes are sexually dimorphic.