Usp22 is expressed in mouse uterus during early pregnancy and involved in endometrial stromal cell decidualization

被引:5
|
作者
Wang, Yaqin [1 ,2 ]
Gao, Yue [1 ,2 ]
Zhou, Chan [3 ,4 ]
Kong, Shuangbo [3 ,4 ]
Wang, Haibin [3 ,4 ]
Yang, Jing [1 ,2 ]
机构
[1] Wuhan Univ, Renmin Hosp, Reprod Med Ctr, Wuhan 430060, Hubei, Peoples R China
[2] Hubei Clin, Res Ctr Assisted Reprod Technol, Wuhan 430060, Hubei, Peoples R China
[3] Xiamen Univ, Affiliated Hosp 1, Reprod Med Ctr, Xiamen 361005, Fujian, Peoples R China
[4] Xiamen Univ, Coll Med, Fujian Prov Key Lab Reprod Hlth Res, Xiamen 361005, Fujian, Peoples R China
来源
CELLS & DEVELOPMENT | 2021年 / 166卷
基金
中国国家自然科学基金;
关键词
Decidualization; Uterine stromal cells; Usp22; Mouse; EMBRYO IMPLANTATION; UBIQUITIN; SAGA; TRANSCRIPTION; FAILURE; SUBUNIT; MARKER;
D O I
10.1016/j.cdev.2021.203681
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
While decidualization is essential for embryo implantation in the context of a normal pregnancy, the molecular basis for this process remains poorly understood. Ubiquitin-specific protease 22 (Usp22), one of the deubiquitinating enzymes, is an important regulator of tumor progression and knocking out this gene in mice results in placental vascular dysplasia and embryonic lethality. In this study, we first demonstrated that Usp22 is spatiotemporally expressed in the mouse peri-implantation uterus. Under artificial decidualization, Usp22 upregulation was detected in both in vivo and in vitro. Progesterone treatment could stimulate Usp22 expression in mouse endometrial stromal cells through progesterone/progesterone receptor (PR) pathway, which is inhibited by PR antagonist. The downregulation of Usp22 within mouse endometrial stomal cells by shRNA impaired their ability to proliferate and undergo decidualization. Taken together, these results suggest that Usp22 is involved in uterine stromal decidualization in mice.
引用
收藏
页数:8
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