A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance.
Abstract
In eutherians, the placenta acts as a barrier and conduit at the maternal-fetal interface.
Syncytiotrophoblasts, the multinucleated cells that cover the placental villous tree
surfaces of the human placenta, are directly bathed in maternal blood and are formed
by the fusion of progenitor cytotrophoblasts that underlie them. Despite their crucial
role in fetal protection, many of the events that govern trophoblast fusion and protection
from microbial infection are unknown. We describe a three-dimensional (3D)-based culture
model using human JEG-3 trophoblast cells that develop syncytiotrophoblast phenotypes
when cocultured with human microvascular endothelial cells. JEG-3 cells cultured in
this system exhibit enhanced fusogenic activity and morphological and secretory activities
strikingly similar to those of primary human syncytiotrophoblasts. RNASeq analyses
extend the observed functional similarities to the transcriptome, where we observed
significant overlap between syncytiotrophoblast-specific genes and 3D JEG-3 cultures.
Furthermore, JEG-3 cells cultured in 3D are resistant to infection by viruses and
Toxoplasma gondii, which mimics the high resistance of syncytiotrophoblasts to microbial
infections in vivo. Given that this system is genetically manipulatable, it provides
a new platform to dissect the mechanisms involved in syncytiotrophoblast development
and microbial resistance.
Type
Journal articleSubject
Cell LineTrophoblasts
Placenta
Humans
Cell Culture Techniques
Gene Expression Profiling
Transcription, Genetic
Pregnancy
Female
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https://hdl.handle.net/10161/22590Published Version (Please cite this version)
10.1126/sciadv.1501462Publication Info
McConkey, Cameron A; Delorme-Axford, Elizabeth; Nickerson, Cheryl A; Kim, Kwang Sik;
Sadovsky, Yoel; Boyle, Jon P; & Coyne, Carolyn B (2016). A three-dimensional culture system recapitulates placental syncytiotrophoblast development
and microbial resistance. Science advances, 2(3). pp. e1501462. 10.1126/sciadv.1501462. Retrieved from https://hdl.handle.net/10161/22590.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Carolyn Coyne
Professor of Molecular Genetics and Microbiology
We study the pathways by which microorganisms cross cellular barriers and the mechanisms
by which these barriers restrict microbial infections. Our studies primarily focus
on the epithelium that lines the gastrointestinal tract and on placental trophoblasts,
the cells that comprise a key cellular barrier of the human placenta. Our work is
highly multidisciplinary and encompasses aspects of cell biology, immunology, and
microbiology. Our long-term goals are to identify pathogen- and host-spe

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