| Literature DB >> 28292466 |
Yanxing Wei1, Xiaohua Zhou2, Wenhao Huang3, Ping Long4, Lu Xiao5, Tian Zhang6, Mei Zhong7, Guangjin Pan8, Yanlin Ma9, Yanhong Yu10.
Abstract
Despite the high incidence of trophoblast-related diseases, the molecular mechanism of inadequate early trophoblast development is still unclear due to the lack of an appropriate cellular model in vitro. In the present study, we reprogrammed the amniotic cells to be induced pluripotent stem cells (iPSCs) via a non-virus and non-integrated method and subsequently differentiated them into trophoblast-like cells by a modified BMP4 strategy in E6 medium. Compared with the previously studied trophoblast-like cells from ESCs, the iPSCs derived trophoblast-like cells behave similarly in terms of gene expression profiles and biofunctions. Also we confirmed the differentiating tendency from iPSCs to be syncytiotrophoblasts-like cells might be caused by inappropriate differentiating oxygen condition. Additionally, we preliminarily indicated in vitro "artificial" differentiation of iPSCs also undergoing a possible trophoblastic stem cell stage, as witnessed in vivo. In conclusion, we provided an in vitro cellular model to study early trophoblast development for specific individual, by using the feasible amnion.Entities:
Keywords: Amnion; BMP4; Differentiation; Induced pluripotent stem cell; Trophoblast
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Year: 2017 PMID: 28292466 DOI: 10.1016/j.placenta.2017.01.121
Source DB: PubMed Journal: Placenta ISSN: 0143-4004 Impact factor: 3.481