Expression and function of Pdcd4 in mouse endometrium during early pregnancy. Issue 4 (April 2018)

• Record Type: Journal Article
• Authors: Zhang, Yue; Ni, Mingyun; Liu, Na; Zhou, Yongjiang; Chen, Xuemei; Ding, Yubin; He, Junlin; Wang, Yingxiong; Liu, Xueqing; Geng, Yanqing; Xie, Liling
• Is Part Of: Reproduction. Volume 155:Issue 4(2018)
• Page Start: 393
• Page End: 402
• Publication Date: 2018-04
• Subjects: Reproduction -- Periodicals; Reproduction -- Molecular aspects -- Periodicals; Reproduction -- Immunological aspects -- Periodicals; Reproduction -- Endocrine aspects -- Periodicals; Fertility -- Periodicals; Human reproduction -- Periodicals; 571.805
• DOI: 10.1530/REP-17-0787
• Languages: English
• ISSNs: 1470-1626

Abstract

Abstract : Embryo implantation is a complex process involving synchronised crosstalk between a receptive endometrium and functional blastocysts. Apoptosis plays an important role in this process as well as in the maintenance of pregnancy. In this study, we analysed the expression pattern of programmed cell death 4 ( Pdcd4 ), a gene associated with apoptosis in the mouse endometrium, during early pregnancy and pseudopregnancy by real-time quantitative polymerase chain reaction, in situ hybridisation, Western blotting and immunohistochemistry. The results showed that Pdcd4 was increased along with days of pregnancy and significantly reduced at implantation sites (IS) from day 5 of pregnancy (D5). The level of Pdcd4 at IS was substantially lower than that at interimplantation sites (IIS) on D6 and D7. In addition, Pdcd4 expression in the endometrium was reduced in response to artificially induced decidualisation in vivo and in vitro . Downregulation of Pdcd4 gene expression in cultured primary stromal cells promoted decidualisation, while upregulation inhibited the decidualisation process by increasing apoptosis. These results demonstrate that Pdcd4 is involved in stromal cell decidualisation by mediating apoptosis and therefore plays a role in embryo implantation in mice.