# Placenta-derived extracellular vesicles in fetal health: emerging insights into brain development and environmental interactions

**Authors:** Ethan Lewis, So Jeong Lee, Hae-Ryung Park

PMC · DOI: 10.1038/s12276-025-01601-2 · Experimental & Molecular Medicine · 2025-12-17

## TL;DR

Placenta-derived extracellular vesicles influence fetal brain development and are affected by environmental factors, offering new insights into fetal health.

## Contribution

This review highlights the role of placental EVs in fetal neurodevelopment and their modulation by environmental stressors.

## Key findings

- Placental EVs transport bioactive cargos that influence fetal brain development and neurogenesis.
- Environmental factors like pollution and infections alter EV content and fetal outcomes.
- EVs can cross maternal-fetal barriers, impacting signaling processes in fetal organ development.

## Abstract

Placenta-derived extracellular vesicles (EVs) are emerging as critical regulators of maternal–fetal communication during pregnancy. These lipid bilayer-enclosed particles, primarily secreted by trophoblasts, transport bioactive cargos—including RNAs, proteins, lipids and neurotransmitters—that influence a wide range of developmental and immunological processes. While much attention has been given to their roles in maternal adaptation and health outcomes, recent studies highlight their direct impact on fetal development, particularly fetal brain development. Emerging evidence suggests that placental EVs may traverse both the placental and blood–brain barriers, thereby contributing to signaling processes that influence neurogenesis, cell fate specification and regional brain patterning. Their cargo composition is dynamic, modulated by gestational age and environmental factors such as air pollution, viral infection and chemical toxicants. These stressors can alter EV secretion and molecular content, contributing to adverse fetal outcomes including impaired organogenesis and neurodevelopmental delays. In this review, we synthesize current knowledge on placental EV biology, examine their roles in maternal and fetal health with an emphasis on neurodevelopment and evaluate how environmental exposures reshape EV-mediated signaling. We also discuss emerging technologies and translational opportunities, including EV-based diagnostics and therapeutic delivery systems. Collectively, placenta-derived EVs represent a vital yet underexplored mechanism in fetal programming, offering novel insights into the developmental origins of health and disease.

Extracellular vesicles (EVs) are tiny particles released by cells that help them communicate. They carry important materials such as proteins and RNA, reflecting the health of the cells they come from. This review focuses on EVs from the placenta, which play a crucial role during pregnancy. These placental EVs help in communication between the mother and fetus, affecting immune responses and fetal development. The study summarized various methods to isolate and analyze these EVs, including advanced techniques such as high-resolution flow cytometry. Researchers stressed that placental EVs can cross barriers between mother and fetus, carrying signals that influence fetal organ development, including the brain. They also emphasized that environmental factors such as pollution can change the content of these EVs, potentially affecting fetal health. The findings suggest that placental EVs are vital for healthy pregnancy outcomes.

This summary was initially drafted using artificial intelligence, then revised and fact-checked by the author.

## Full-text entities

- **Diseases:** neurodevelopmental delays (MESH:D006968), infection (MESH:D007239), viral (MESH:D014777)
- **Chemicals:** lipid (MESH:D008055)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12800091/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12800091/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12800091/full.md

---
Source: https://tomesphere.com/paper/PMC12800091