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Updated: Jun 27, 2026

Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
Published on: January 26, 2024
Placenta-Derived Extracellular Vesicles (pdEVs): Key Mediators That Affect the Metabolic Health of Offspring in Early
Hanmo Lin1, Chuhan Shao1, Jie Yu1
1Key Laboratory of Endocrinology, Ministry of Health, Department of Endocrinology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Insights
Placenta extracellular vesicles (EVs) transfer signals from mothers to fetuses, influencing offspring metabolic health. These EVs, altered by maternal nutrition, may cause long-term metabolic disease susceptibility.
Area of Science:
- Reproductive biology
- Metabolic programming
- Perinatal medicine
Background:
- Maternal nutrition significantly impacts offspring metabolic health.
- Placenta-derived extracellular vesicles (EVs) mediate maternal-fetal communication.
- Adverse conditions like obesity and gestational diabetes alter EV cargo (miRNAs, proteins).
Purpose of the Study:
- To review evidence on placental EVs in metabolic programming.
- To evaluate the role of EVs in offspring metabolic health.
- To identify knowledge gaps and therapeutic potential.
Main Methods:
- Review of in vivo and in vitro studies.
- Analysis of EV composition and function.
- Examination of proposed molecular pathways (e.g., β-cell function, lipogenesis, angiogenesis, inflammation, epigenetics).
Main Results:
- Placental EVs transmit maternal signals, influencing fetal development and metabolic programming.
- EVs impact offspring pancreatic β-cells, lipogenesis, angiogenesis, inflammation, and epigenetic modifications.
- Evidence suggests placental EVs contribute to long-term metabolic phenotypes and disease risk.
Conclusions:
- Placental EVs are critical messengers in maternal-fetal metabolic programming.
- Further research, including human studies and mechanistic validation, is needed.
- Placental EVs show potential as biomarkers and therapeutic targets for metabolic disorders.
Abstract:
Placenta-derived extracellular vesicles (EVs), particularly exosomes, serve as key mediators that influence metabolic programming in offspring under adverse early nutritional conditions, such as maternal obesity or gestational diabetes. They respond to maternal nutritional disturbances-such as obesity or gestational diabetes-by altering the composition of the miRNAs and proteins they carry. Evidence from in vivo and in vitro studies suggests that these modified EVs influence offspring metabolic programming through multiple putative pathways: regulating fetal pancreatic β-cell development and function, modulating lipogenesis via PPARγ signaling, affecting placental angiogenesis, and promoting inflammation and epigenetic alterations. By transmitting maternal environmental signals to the fetus, placental EVs are hypothesized to contribute to long-term metabolic phenotypes and disease susceptibility. This review critically examines the current evidence positioning placental EVs as key messengers in maternal-fetal communication, evaluates the strength of evidence supporting their role in shaping offspring metabolic health, identifies major knowledge gaps (e.g., limited direct evidence in human offspring, lack of standardized isolation methods), and suggests their potential as early intervention biomarkers or therapeutic targets for preventing metabolic disorders in offspring. We also highlight the need for prospective cohort studies and mechanistic validation in appropriate animal models to establish causality.
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