1. Academic Validation
  2. Trophoblast fusion in fetal growth restriction is inhibited by CTGF in a cell-cycle-dependent manner

Trophoblast fusion in fetal growth restriction is inhibited by CTGF in a cell-cycle-dependent manner

  • J Mol Histol. 2024 Aug 10. doi: 10.1007/s10735-024-10239-9.
Ketong Liu 1 Suwen Wu 1 2 Yutong Cui 1 Xiang Tao 1 Yanhong Li 3 Xirong Xiao 4 5
Affiliations

Affiliations

  • 1 Obstetrics and Gynecology Hospital of Fudan University, Fangxie Road 419, Shanghai, 200011, China.
  • 2 Department of Ultrasound Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430050, China.
  • 3 Obstetrics and Gynecology Hospital of Fudan University, Fangxie Road 419, Shanghai, 200011, China. lyh198920@aliyun.com.
  • 4 Obstetrics and Gynecology Hospital of Fudan University, Fangxie Road 419, Shanghai, 200011, China. xiaoxirong@fudan.edu.cn.
  • 5 Kashi Prefecture Second People's Hospital, Jiankang Road 1, Kashgar, 844000, China. xiaoxirong@fudan.edu.cn.
Abstract

Fetal growth restriction (FGR) is a relatively common complication of pregnancy, and insufficient syncytialization in the placenta may play an important role in the pathogenesis of FGR. However, the mechanism of impaired formation of the syncytiotrophoblast layer in FGR patients requires further exploration. In the present study, we demonstrated that the level of syncytialization was decreased in FGR patient placentas, while the expression of connective tissue growth factor (CTGF) was significantly upregulated. CTGF was found to inhibit trophoblast fusion via regulating cell cycle progress of BeWo cells. Furthermore, we found that CTGF negatively regulates cell cycle arrest in a p21-dependent manner as overexpression of p21 could rescue the impaired syncytialization induced by CTGF-overexpression. Besides, we also identified that CTGF inhibits the expression of p21 through ITGB4/PI3K/Akt signaling pathway. Our study provided a new insight for elucidating the pathogenic mechanism of FGR and a novel idea for the clinical therapy of FGR.

Keywords

CTGF; Cell cycle; Fetal growth restriction; Syncytialization; Trophoblast; p21.

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