Polystyrene microplastics impair trophoblast invasion in vitro and alter microRNA expression targeting the

Saikanth Varma1, Asim K Duttaroy2, Sanjay Basak1

  • 1Molecular Biology Division, ICMR-National Institute of Nutrition, Indian Council of Medical Research, India.

Insights

Polystyrene microplastics (PS-MPs) exposure impairs trophoblast invasion and alters microRNA (miRNA) expression crucial for placental development. This impacts angiogenesis and activates hypoxia mediators, affecting early placental functions.

Area of Science:

  • Environmental Health
  • Reproductive Biology
  • Molecular Toxicology

Background:

  • Human exposure to microplastics (MPs) is confirmed by their presence in blood and placenta.
  • Trophoblast invasion is critical for normal placental development.
  • The impact of MPs on placental microRNA (miRNA) expression and trophoblast function is largely unknown.

Purpose of the Study:

  • To investigate the effects of polystyrene microplastics (PS-MPs) on trophoblast cells (HTR8/SVneo).
  • To analyze changes in miRNA, gene, and protein expression related to angiogenesis and hypoxia.
  • To understand the impact of PS-MPs on trophoblast invasion and placental function.

Main Methods:

  • Utilized the HTR8/SVneo trophoblast cell line.
  • Investigated PS-MPs interaction using Scanning Electron Microscopy (SEM).
  • Assessed miRNA, gene, and protein expression, focusing on angiogenic and hypoxia pathways.

Main Results:

  • SEM confirmed PS-MPs adherence and accumulation on trophoblast cell membranes.
  • PS-MPs significantly reduced trophoblast invasion.
  • Altered expression of vascular endothelial growth factor (VEGF) and its receptors was observed.
  • Increased expression of angiogenesis-regulating miRNAs and dysregulated miRNAs linked to inadequate trophoblast invasion were detected.

Conclusions:

  • PS-MP exposure negatively impacts trophoblast invasion.
  • Exposure alters trophoblast miRNA expression, targeting VEGF.
  • PS-MPs activate hypoxia mediators, potentially disrupting early placental functions.

Related Concept Videos