AI Article Synopsis

  • Extracellular vesicles (EVs) play important roles in various physiological and disease conditions, including pregnancy, serving as biomarkers and communicators between the placenta and both mother and fetus.
  • The study focuses on isolating small EVs from first trimester placental explants, investigating both normal conditions and those affected by human cytomegalovirus infection.
  • Findings revealed that infection alters several surface marker expressions but does not impact EV secretion or integrity, setting the stage for understanding EV functions in early pregnancy and identifying new biomarkers for congenital infections.

Article Abstract

Extracellular vesicles (EVs) have increasingly been recognized as key players in a wide variety of physiological and pathological contexts, including during pregnancy. Notably, EVs appear both as possible biomarkers and as mediators involved in the communication of the placenta with the maternal and fetal sides. A better understanding of the physiological and pathological roles of EVs strongly depends on the development of adequate and reliable study models, specifically at the beginning of pregnancy where many adverse pregnancy outcomes have their origin. In this study, we describe the isolation of small EVs from a histoculture model of first trimester placental explants in normal conditions as well as upon infection by human cytomegalovirus. Using bead-based multiplex cytometry and electron microscopy combined with biochemical approaches, we characterized these small EVs and defined their associated markers and ultrastructure. We observed that infection led to changes in the expression level of several surface markers, without affecting the secretion and integrity of small EVs. Our findings lay the foundation for studying the functional role of EVs during early pregnancy, along with the identification of new predictive biomarkers for the severity and outcome of this congenital infection, which are still sorely lacking.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461063PMC
http://dx.doi.org/10.3389/fcell.2021.689122DOI Listing

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