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Published on: January 26, 2024
The functions of microparticles in pre-eclampsia
Joris A M van der Post1, Christianne A R Lok, Kees Boer
1Department of Obstetrics and Gynaecology, Academic Medical Center, Amsterdam, The Netherlands.
Seminars in Thrombosis and Hemostasis
|March 4, 2011
Summary
Pre-eclampsia, a pregnancy disorder causing hypertension, involves placental microparticles like syncytiotrophoblast microparticles (STBM). This review explores STBM and other microparticles in pre-eclampsia pathogenesis.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Cell Biology
Background:
- Pre-eclampsia (P-EC) is a significant pregnancy complication affecting 2-5% of pregnancies, leading to maternal and perinatal morbidity and mortality.
- Characterized by hypertension and proteinuria, P-EC's exact cause is unknown but linked to placental factors causing inflammation and endothelial dysfunction.
- Placenta-derived microparticles, particularly syncytiotrophoblast microparticles (STBM), are increasingly recognized as key contributors to P-EC pathogenesis.
Purpose of the Study:
- To review the presence and functions of syncytiotrophoblast microparticles (STBM).
- To discuss the role of other cell-derived microparticles and exosomes in pre-eclampsia.
- To consolidate current understanding of microparticle involvement in P-EC.
Main Methods:
- Literature review focusing on placental microparticles and exosomes.
- Analysis of studies investigating STBM and other extracellular vesicles in pre-eclampsia.
- Synthesis of evidence on the biological functions of these microparticles.
Main Results:
- STBM are consistently found in maternal circulation during pre-eclampsia.
- These microparticles contribute to systemic inflammation and endothelial dysfunction.
- Other extracellular vesicles may also play a role in the disease process.
Conclusions:
- Syncytiotrophoblast microparticles (STBM) are crucial mediators in pre-eclampsia.
- Understanding STBM and other microparticles offers potential diagnostic and therapeutic targets.
- Further research into extracellular vesicles is warranted for P-EC management.

