Participation of COX2/mPGES1/PGE2 in mouse and human endometrial stromal decidualization
(2025) In BMC Veterinary Research 21(1).- Abstract
Background: Prostaglandin E2 (PGE2) is vital for embryo implantation and decidualization. Whether COX2/mPGES1/PGE2 pathway is essential for mouse and human decidualization remains unclear. Results: This study showed that mPGES1 was highly expressed in the mouse uterus’s subluminal stromal cells at the implantation site. COX2-specific inhibitor Valdecoxib and mPGES1 selective inhibitor MK886 were used to analyze the roles of mPGES1 and COX2 during mouse and human decidualization. During mouse in vitro decidualization, decidua/trophoblast prolactin-related protein (Dtprp) expression was significantly suppressed by Valdecoxib and MK886. Under human in vitro decidualization, mPGES1 significantly increases, while both cPGES and mPGES2 remain... (More)
Background: Prostaglandin E2 (PGE2) is vital for embryo implantation and decidualization. Whether COX2/mPGES1/PGE2 pathway is essential for mouse and human decidualization remains unclear. Results: This study showed that mPGES1 was highly expressed in the mouse uterus’s subluminal stromal cells at the implantation site. COX2-specific inhibitor Valdecoxib and mPGES1 selective inhibitor MK886 were used to analyze the roles of mPGES1 and COX2 during mouse and human decidualization. During mouse in vitro decidualization, decidua/trophoblast prolactin-related protein (Dtprp) expression was significantly suppressed by Valdecoxib and MK886. Under human in vitro decidualization, mPGES1 significantly increases, while both cPGES and mPGES2 remain unchanged. PGE2-mediated upregulation of insulin growth factor binding protein 1 (IGFBP1) was significantly inhibited by Valdecoxib and MK886. Conclusions: Our findings suggest the involvement of COX2/mPGES1/PGE2 pathway in both mouse and human decidualization.
(Less)
- author
- Wang, Peng Chao
; Liu, Jie
; Liu, Yue Fang
; Wu, Yang
; Xue, Lin Li
and Yang, Zhen Shan
LU
- organization
- publishing date
- 2025
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- COX2, Decidualization, Endometrial stromal cell, mPGES1, PGE2
- in
- BMC Veterinary Research
- volume
- 21
- issue
- 1
- article number
- 43
- publisher
- BioMed Central (BMC)
- external identifiers
-
- pmid:39885565
- scopus:85217357902
- ISSN
- 1746-6148
- DOI
- 10.1186/s12917-025-04505-5
- language
- English
- LU publication?
- yes
- id
- d5de3fd5-6b0e-4f69-bca8-1a35ef538bdb
- date added to LUP
- 2025-03-20 13:51:20
- date last changed
- 2025-07-10 22:34:23
@article{d5de3fd5-6b0e-4f69-bca8-1a35ef538bdb, abstract = {{<p>Background: Prostaglandin E2 (PGE2) is vital for embryo implantation and decidualization. Whether COX2/mPGES1/PGE2 pathway is essential for mouse and human decidualization remains unclear. Results: This study showed that mPGES1 was highly expressed in the mouse uterus’s subluminal stromal cells at the implantation site. COX2-specific inhibitor Valdecoxib and mPGES1 selective inhibitor MK886 were used to analyze the roles of mPGES1 and COX2 during mouse and human decidualization. During mouse in vitro decidualization, decidua/trophoblast prolactin-related protein (Dtprp) expression was significantly suppressed by Valdecoxib and MK886. Under human in vitro decidualization, mPGES1 significantly increases, while both cPGES and mPGES2 remain unchanged. PGE2-mediated upregulation of insulin growth factor binding protein 1 (IGFBP1) was significantly inhibited by Valdecoxib and MK886. Conclusions: Our findings suggest the involvement of COX2/mPGES1/PGE2 pathway in both mouse and human decidualization.</p>}}, author = {{Wang, Peng Chao and Liu, Jie and Liu, Yue Fang and Wu, Yang and Xue, Lin Li and Yang, Zhen Shan}}, issn = {{1746-6148}}, keywords = {{COX2; Decidualization; Endometrial stromal cell; mPGES1; PGE2}}, language = {{eng}}, number = {{1}}, publisher = {{BioMed Central (BMC)}}, series = {{BMC Veterinary Research}}, title = {{Participation of COX2/mPGES1/PGE2 in mouse and human endometrial stromal decidualization}}, url = {{http://dx.doi.org/10.1186/s12917-025-04505-5}}, doi = {{10.1186/s12917-025-04505-5}}, volume = {{21}}, year = {{2025}}, }