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

被引:0
作者
Liu, Ketong [1 ]
Wu, Suwen [1 ,3 ]
Cui, Yutong [1 ]
Tao, Xiang [1 ]
Li, Yanhong [1 ]
Xiao, Xirong [1 ,2 ]
机构
[1] Fudan Univ, Obstet & Gynecol Hosp, 419 Fangxie Rd, Shanghai 200011, Peoples R China
[2] Kashi Prefecture Second Peoples Hosp, Jiankang Rd 1, Kashgar 844000, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Ultrasound Med, Wuhan, Peoples R China
基金
美国国家科学基金会;
关键词
Fetal growth restriction; Trophoblast; Syncytialization; Cell cycle; CTGF; p21; DOWN-REGULATION; SINGLE-CELL; EXPRESSION; DIFFERENTIATION; CCN2/CTGF; INVASION; NETWORK; ARREST;
D O I
10.1007/s10735-024-10239-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:895 / 908
页数:14
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