PLAC8, a new marker for human interstitial extravillous trophoblast cells, promotes their invasion and migration

Author:

Chang Wen-Lin123ORCID,Liu Ya-Wei14ORCID,Dang Yan-Li5ORCID,Jiang Xiang-Xiang14,Xu Honglin6,Huang Xing1ORCID,Wang Yan-Ling1,Wang Haibin1,Zhu Cheng1,Xue Li-Qun3ORCID,Lin Hai-Yan1,Meng Wenxiang6,Wang Hongmei1ORCID

Affiliation:

1. State key laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, PR China

2. Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Institute of Urology, Peking University Shenzhen Hospital, Biomedical Research Institute, Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen 518036, PR China

3. College of Veterinary Medicine, Hunan Agricultural University, Changsha 410128, PR China

4. University of Chinese Academy of Sciences, Beijing 100039, PR China

5. Department of Obstetrics and Gynecology, the 306th Hospital of PLA, Beijing 100101, PR China

6. State key laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100190, PR China

Abstract

Proper differentiation of trophoblast cells in the human placenta is a prerequisite for a successful pregnancy, and dysregulation of this process may lead to malignant pregnancy outcomes, such as preeclampsia. Finding specific markers for different types of trophoblast cells is essential to understand trophoblast differentiation. Here we report that placenta-specific protein 8 (PLAC8) is specifically expressed in the interstitial extravillous trophoblast cells (iEVTs) on the fetomaternal interface. Utilizing model systems including placental villi-decidua co-culture, iEVTs induction by using primary trophoblast cells or explants, etc, we found that PLAC8 promotes invasion and migration of iEVTs. Mechanistically, time-lapse imaging, GTPase activity assay, co-IP and RNA-seq studies show that PLAC8 increases the Cdc42 and Rac1 activities and further induces the formation of filopodia at the leading edge of the migratory trophoblast cells. More interestingly, PLAC8 is significantly upregulated under hypoxia and expression of PLAC8 is higher in iEVTs from preeclamptic placentas as compared to those from the normal control placentas. Together, PLAC8 is a new marker for iEVTs and play an important role in promoting trophoblast invasion and migration.

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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