Mechanism of human chorionic gonadotropin in endometrial receptivity via the miR‐126‐3p/PI3K/Akt/eNOS axis

Bibliographic Details
Title: Mechanism of human chorionic gonadotropin in endometrial receptivity via the miR‐126‐3p/PI3K/Akt/eNOS axis
Authors: Wei Wang, Liang Ge, Li‐Li Zhang, Li‐Rong Wang, Yong‐Yan Lu, Li Gou, Rui‐Qiang Gou, Tong‐Yu Xu, Xiao‐Ling Ma, Xue‐Hong Zhang
Source: Kaohsiung Journal of Medical Sciences, Vol 39, Iss 5, Pp 468-477 (2023)
Publisher Information: Wiley, 2023.
Publication Year: 2023
Collection: LCC:Medicine (General)
Subject Terms: Akt, human chorionic gonadotropin, miR‐126‐3p, PI3K, PIK3R2, Medicine (General), R5-920
More Details: Abstract Human chorionic gonadotropin (hCG) might affect endometrial receptivity, exerting integral roles in embryo implantation. This study explored the action of hCG in endometrial receptivity via the miR‐126‐3p/PIK3R2/PI3K/Akt/eNOS axis. The embryo implantation dysfunction (EID) mouse models were established by administrating mifepristone and human endometrial epithelial cells (EECs) were used for in vivo experiments, both followed by hCG treatment. Expression level of CD105 and protein levels of cadherin CD144 and CD146 in mice were determined by immunohistochemistry and Western blot. The levels of miR‐126‐3p and PIK3R2 mRNA and PIK3R2, p‐PI3K p85 α, PI3K p110 α, p‐Akt, Akt, p‐eNOS, and eNOS protein levels were measured. Cell proliferation was evaluated by CCK‐8 and EdU assays. The binding sites of miR‐126‐3p and PIK3R2 were predicted and verified. hCG‐treated EECs were further transfected with miR‐126‐inhibitor for functional rescue experiments. hCG ameliorated endometrial receptivity in EID mice. Moreover, hCG promoted miR‐126‐3p and suppressed PIK3R2 in EID mice and EECs. miR‐126‐3p targeted PIK3R2. EEC proliferation was enhanced after hCG treatment but inhibited by miR‐126‐3p downregulation. Both in vivo and in vitro experiments validated that hCG activated the PI3K/Akt/eNOS pathway through the miR‐126‐3p/PIK3R2 axis. Collectively, hCG improves endometrial receptivity by activating the PI3K/Akt/eNOS pathway via regulating miR‐126‐3p/PIK3R2.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2410-8650
1607-551X
Relation: https://doaj.org/toc/1607-551X; https://doaj.org/toc/2410-8650
DOI: 10.1002/kjm2.12672
Access URL: https://doaj.org/article/3ef2b08f846a461cbe90c6f75ff5e41f
Accession Number: edsdoj.3ef2b08f846a461cbe90c6f75ff5e41f
Database: Directory of Open Access Journals
More Details
ISSN:24108650
1607551X
DOI:10.1002/kjm2.12672
Published in:Kaohsiung Journal of Medical Sciences
Language:English