Shear stress in the intervillous space promotes syncytial formation of iPS cells-derived trophoblasts

Author:

Inohaya Asako12,Chigusa Yoshitsugu12,Takakura Masahito12,Io Shingo12,Kim Min-A34,Matsuzaka Yu12,Yasuda Eriko12,Ueda Yusuke12,Kawamura Yosuke12,Takamatsu Shiro12,Mogami Haruta12,Takashima Yasuhiro56,Mandai Masaki12,Kondoh Eiji78

Affiliation:

1. Department of Gynecology and Obstetrics , Graduate School of Medicine, , Kyoto , Japan

2. Kyoto University , Graduate School of Medicine, , Kyoto , Japan

3. Department of Obstetrics and Gynecology , Gangnam Severance Hospital, , Seoul , Korea

4. Yonsei University College of Medicine , Gangnam Severance Hospital, , Seoul , Korea

5. Department of Life Science Frontiers , Center for iPS Cell Research and Application, , Kyoto Japan

6. Kyoto University , Center for iPS Cell Research and Application, , Kyoto Japan

7. Department of Obstetrics and Gynecology , Faculty of Life Sciences, , Kumamoto , Japan

8. Kumamoto University , Faculty of Life Sciences, , Kumamoto , Japan

Abstract

Abstract The intervillous space of human placenta is filled with maternal blood, and villous trophoblasts are constantly exposed to the shear stress generated by maternal blood pressure and flow throughout the entire gestation period. However, the effects of shear stress on villous trophoblasts and their biological significance remain unknown. Here, using our recently established naïve human pluripotent stem cells-derived cytotrophoblast stem cells (nCTs) and a device that can apply arbitrary shear stress to cells, we investigated the impact of shear stress on early-stage trophoblasts. After 72 h of exposure to 10 dyn/cm2 shear stress, nCTs became fused and multinuclear, and mRNA expression of the syncytiotrophoblast (ST) markers, such as glial cell missing 1, endogenous retrovirus group W member 1 envelope, chorionic gonadotropin subunit beta 3, syndecan 1, pregnancy specific beta-1-glycoprotein 3, placental growth factor, and solute carrier family 2 member 1 were significantly upregulated compared to static conditions. Immunohistochemistry showed that shear stress increased fusion index, human chorionic gonadotropin secretion, and human placental lactogen secretion. Increased microvilli formation on the surface of nCTs under flow conditions was detected using scanning electron microscopy. Intracellular cyclic adenosine monophosphate significantly increased under flow conditions. Moreover, transcriptome analysis of nCTs subjected to shear stress revealed that shear stress upregulated ST-specific genes and downregulated CT-specific genes. Collectively, these findings indicate that shear stress promotes the differentiation of nCTs into ST.

Funder

Ministry of Education, Science, Culture, and Sports, Japan

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,General Medicine,Reproductive Medicine

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