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PIBF1 regulates trophoblast syncytialization and promotes cardiovascular development

Cited 1 time in Web of Science Cited 1 time in Scopus
Authors

Lee, Jong Geol; Yon, Jung-Min; Kim, Globinna; Lee, Seul-Gi; Kim, C-Yoon; Cheong, Seung-A; Kim, Hyun-Yi; Yu, Jiyoung; Kim, Kyunggon; Sung, Young Hoon; Yoo, Hyun Ju; Woo, Dong-Cheol; Rho, Jin Kyung; Ha, Chang Hoon; Pack, Chan-Gi; Oh, Seak Hee; Lim, Joon Seo; Han, Yu Mi; Hong, Eui-Ju; Seong, Je Kyung; Lee, Han-Woong; Lee, Sang-Wook; Lee, Ki-Up; Kim, Chong Jai; Nam, Sang-Yoon; Cho, You Sook; Baek, In-Jeoung

Issue Date
2024-02
Publisher
Nature Publishing Group
Citation
Nature Communications, Vol.15 No.1, p. 1487
Abstract
Proper placental development in early pregnancy ensures a positive outcome later on. The developmental relationship between the placenta and embryonic organs, such as the heart, is crucial for a normal pregnancy. However, the mechanism through which the placenta influences the development of embryonic organs remains unclear. Trophoblasts fuse to form multinucleated syncytiotrophoblasts (SynT), which primarily make up the placental materno-fetal interface. We discovered that endogenous progesterone immunomodulatory binding factor 1 (PIBF1) is vital for trophoblast differentiation and fusion into SynT in humans and mice. PIBF1 facilitates communication between SynT and adjacent vascular cells, promoting vascular network development in the primary placenta. This process affected the early development of the embryonic cardiovascular system in mice. Moreover, in vitro experiments showed that PIBF1 promotes the development of cardiovascular characteristics in heart organoids. Our findings show how SynTs organize the barrier and imply their possible roles in supporting embryogenesis, including cardiovascular development. SynT-derived factors and SynT within the placenta may play critical roles in ensuring proper organogenesis of other organs in the embryo.
ISSN
2041-1723
URI
https://hdl.handle.net/10371/204955
DOI
https://doi.org/10.1038/s41467-024-45647-8
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Metabolic syndrome model construction and omics research, Mouse locomotion and metabolic phenotyping analysis, Study of immune regulatory response in obesity, 대사증후군 모델 구축 및 오믹스 연구, 마우스 운동 및 대사 표현형 분석, 비만에서의 면역 조절 반응 연구

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