Inefficient development of syncytiotrophoblasts in the Atp11a -deficient mouse placenta

Author:

Ochiai Yuki1,Suzuki Chigure23,Segawa Katsumori1,Uchiyama Yasuo23,Nagata Shigekazu14ORCID

Affiliation:

1. Laboratory of Biochemistry and Immunology, Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan

2. Department of Cellular and Molecular Pharmacology, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan

3. Department of Cellular and Neuropathology, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan

4. Center for Infectious Disease Education and Research, Osaka University, Suita 565-0871, Japan

Abstract

Significance Plasma membranes are composed of a lipid bilayer in which phosphatidylserine (PtdSer) is confined to the inner leaflet by the action of flippase that translocates PtdSer from the outer to inner leaflets. Two P4-ATPases (ATP11A and ATP11C) work as flippase at plasma membranes. Here, we report that the mouse placenta expresses only ATP11A, and Atp11a- deficient mouse embryos die during embryogenesis due to inefficient formation of syncytiotrophoblasts in the placental labyrinth. The flippase-null mutation inactivates human choriocarcinoma BeWo cells to translocate PtdSer into the inner leaflet and undergo cell fusion. These findings highlight the importance of flippase to regulate the distribution of phospholipids for cell fusion, at least in trophoblast fusion.

Funder

MEXT | Japan Society for the Promotion of Science

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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