Authors
Hanin Alahmadi, Allison Harbolic, Christopher De Oliveira-Cordova, Raulle Reynolds, Michelle Jojy, Courtney Potts, Sofia Doan, Tanvi Mathur, Mohammad Saiful Islam, Melisa J Andrade, Quinton Smith, Phoebe A Stapleton, Somenath Mitra, Genoa R Warner
Published in
Reproductive toxicology (Elmsford, N.Y.). Pages 109331. Aug 20, 2026. Epub Aug 20, 2026.
Abstract
Plastic production has been increasing exponentially. Throughout their lifespan, plastics degrade into smaller particles that accumulate in our bodies and the environment. Recent studies found these plastic particles can cross the placental barrier and reach the fetus. However, the impact of plastic particles on placental function is still unknown. We hypothesized that nanoplastics would disrupt placental growth and function, specifically focusing on transforming growth factor beta (TGFβ) signaling. To understand the impact of plastic particles on the placenta, we orally exposed pregnant CD-1 mice to 50nm or 200nm polystyrene plastic particles from gestation day 8 to day 15 at a human-relevant concentration of 5mg/kg/day. After euthanasia on day 15, placenta and fetus weights were recorded, and tissues were prepared for histomorphology and gene expression analysis. We observed a statistically significant decrease in the area of the decidua in the placentas for the 200nm treatment group and a borderline significant decrease in decidua area for the 50nm treatment group compared to control. However, when separated by sex, only the male decidua were significantly decreased in the 200nm group. Gene expression analysis of key signaling factors in the TGFβ pathway identified increased expression of Smad2 and Smad3, which may be suppressing estrogen receptor signaling. Overall, both particle sizes disrupted placenta structure and signaling in a sex-dependent manner.
PMID:
42624384
Bibliographic data and abstract were imported from PubMed on 21 Aug 2026.
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