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Published in: Current Hypertension Reports 9/2016

Open Access 01-09-2016 | Preeclampsia (V Garovic, Section Editor)

Preeclampsia and Extracellular Vesicles

Authors: Sarwat I. Gilani, Tracey L. Weissgerber, Vesna D. Garovic, Muthuvel Jayachandran

Published in: Current Hypertension Reports | Issue 9/2016

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Abstract

Preeclampsia is a hypertensive pregnancy disorder characterized by development of hypertension and proteinuria after 20 weeks of gestation that remains a leading cause of maternal and neonatal morbidity and mortality. While preeclampsia is believed to result from complex interactions between maternal and placental factors, the proximate pathophysiology of this syndrome remains elusive. Cell-to-cell communication is a critical signaling mechanism for feto-placental development in normal pregnancies. One mechanism of cellular communication relates to activated cell-derived sealed membrane vesicles called extracellular vesicles (EVs). The concentrations and contents of EVs in biological fluids depend upon their cells of origin and the stimuli which trigger their production. Research on EVs in preeclampsia has focused on EVs derived from the maternal vasculature (endothelium, vascular smooth muscle) and blood (erythrocytes, leukocytes, and platelets), as well as placental syncytiotrophoblasts. Changes in the concentrations and contents of these EVs may contribute to the pathophysiology of preeclampsia by accentuating the pro-inflammatory and pro-coagulatory states of pregnancy. This review focuses on possible interactions among placental- and maternal-derived EVs and their contents in the initiation and progression of the pathogenesis of preeclampsia. Understanding the contributions of EVs in the pathogenesis of preeclampsia may facilitate their use as diagnostic and prognostic biomarkers.
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Metadata
Title
Preeclampsia and Extracellular Vesicles
Authors
Sarwat I. Gilani
Tracey L. Weissgerber
Vesna D. Garovic
Muthuvel Jayachandran
Publication date
01-09-2016
Publisher
Springer US
Published in
Current Hypertension Reports / Issue 9/2016
Print ISSN: 1522-6417
Electronic ISSN: 1534-3111
DOI
https://doi.org/10.1007/s11906-016-0678-x