Publication: Endometrial androgen signaling and decidualization regulate trophoblast expansion and invasion in co-culture: A time-lapse study
Issued Date
2016-11-01
Resource Type
ISSN
15323102
01434004
01434004
Other identifier(s)
2-s2.0-84988001476
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Mahidol University
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SCOPUS
Bibliographic Citation
Placenta. Vol.47, (2016), 56-62
Suggested Citation
Thanyarat Wongwananuruk, Tomomi Sato, Takeshi Kajihara, Sachiko Matsumoto, Masumi Akita, Kazuhiro Tamura, Jan J. Brosens, Osamu Ishihara Endometrial androgen signaling and decidualization regulate trophoblast expansion and invasion in co-culture: A time-lapse study. Placenta. Vol.47, (2016), 56-62. doi:10.1016/j.placenta.2016.09.005 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/42912
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Title
Endometrial androgen signaling and decidualization regulate trophoblast expansion and invasion in co-culture: A time-lapse study
Abstract
© 2016 Elsevier Ltd Introduction To elucidate whether trophoblast expansion and invasion are modulated by androgen signaling in an in vitro co-culture model system with decidualizing endometrial stromal cells (ESCs). Methods We employed an in vitro co-culture model of early embryo implantation, consisting of human ESCs (EtsT499 cells) and spheroids generated by extravillous trophoblast (EVT) derived HTR8/Svneo. The ESCs were decidualized with 8-bromo-cAMP (8-br-cAMP) in the presence or absence of dihydrotestosterone (DHT) at various concentrations for 5 days before co-culture with EVT spheroids. Trophoblast expansion was monitored by fluorescent time-lapse imaging microscopy. ESCs motility was visualized by using CellTracker™ Orange CMRA fluorescent probe. Apoptosis of ESCs was detected by CellEvent™ Caspase-3/7® green detection reagent. Invasion assays were performed to quantify EVT invasion through a chemotaxis cell membrane. Results Expansion of EVT spheroids was significantly enhanced by decidualized compared to undifferentiated ESCs. This process was further stimulated if ESCs were first decidualized in the presence of DHT. In contrast to decidualized ESCs, undifferentiated cells actively migrated away from expanding EVT spheroids. Invasiveness of EVT toward decidualized ESCs was significantly attenuated in comparison to undifferentiated ESCs. DHT had no effect on EVT invasion. However, an inhibitor of intercellular gap junction communication significantly enhanced EVT invasion towards decidualized ESCs. Conclusions These results indicate distinct roles for androgen signaling and gap junction formation in decidual cells in regulating trophoblast expansion and invasion.