The Essential Role of PGF2α/PTGFR in Molding Endometrial Breakdown and Vascular Dynamics, Regulated by HIF-1α in a Mouse Menstrual-like Model

In: Reproductive Sciences · 2024 · vol. 31(9) , pp. 2718–2730 · doi:10.1007/s43032-024-01526-7 · PMID:38637474 · W4394932939
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PGF2α signaling through PTGFR, regulated by HIF-1α binding to the Ptgfr promoter, drives endometrial breakdown and vascular changes during menstruation in mice.

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This study investigated which prostaglandin pathways regulate endometrial disintegration during menstruation, using a mouse menstrual-like model with analyses of histology and prostaglandin/receptor expression. Concentrations of PGE1, PGE2, and PGF2α increased during endometrial breakdown, and progesterone withdrawal led to early increases in Ptgfr mRNA and later rises in PTGFR protein; PTGFR inhibition with AL8810 suppressed breakdown and shedding while increasing angiostatin and reducing VEGF-A and vascular permeability. The authors found that HIF-1α directly bound the Ptgfr promoter and that both HIF-1α and PTGFR were localized mainly to luminal/gland epithelium, vascular endothelium, and the pre-decidual zone, with a HIF-1α inhibitor (2-methoxyestradiol) similarly reducing PTGFR expression and breakdown. The paper’s findings are limited to a mouse menstrual-like system and in vitro human stromal cell relevance rather than direct clinical validation. This paper is centrally about endometriosis-focused menstruation biology — specifically, it elucidates PGF2α/PTGFR and HIF-1α–regulated mechanisms of endometrial breakdown and vascular dynamics that are relevant to endometriosis pathophysiology.

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Abstract

In women of childbearing age, extensive decidualization, shedding and remodeling of the endometrium during the menstrual cycle are fundamental for successful pregnancy. The role of prostaglandins (PGs) in menstruation has long been proposed in humans, and the rate-limiting enzyme cyclooxygenase was shown to play a key role in endometrial breakdown and shedding in a mouse menstrual-like model in our previous study. However, the specific types of PGs involved and their respective roles remain unclear. Therefore, our objective was to investigate the mechanism through which PGs regulate endometrial disintegration. In this study, the microscopy was observed by HE; the protein levels of prostaglandins E1 (PGE1), prostaglandins E2 (PGE2), prostaglandin F2α (PGF2α) and Prostaglandin I2 (PGI2) were detected by ELISA; the mRNA level of Pfgfr2, Vascular Endothelial Growth Factor(Vegf), Angiostatin and Hypoxia inducible factor-1α (Hif1α) were examined by real-time PCR; PTGFR Receptor (PTGFR), VEGF, Angiostatin and HIF-1α protein levels were investigated by western blotting; the locations of protein were observed by Immunohistochemistry; HIF-1α binding PTGFR promoter was detected by Chromatin Immunoprecipitation (ChIP) and real-time PCR. We found that the concentrations of PGE1, PGE2, and PGF2α all increased significantly during this process. Furthermore, Ptgfr mRNA increased soon after Progesterone (P4) withdrawal, and PTGFR protein levels increased significantly during abundant endometrial breakdown and shedding processes. PTGFR inhibitors AL8810 significantly suppressed endometrial breakdown and shedding, promoted Angiostatin expression, and reduced VEGF-A expressions and vascular permeability. And HIF-1α and PTGFR were mainly located in the luminal/gland epithelium, vascular endothelium, and pre-decidual zone. Interestingly, HIF-1α directly bound to Ptgfr promoter. Moreover, a HIF-1α inhibitor 2-methoxyestradiol (2ME) significantly reduced PTGFR expression and suppressed endometrial breakdown which was in accord with PTGFR inhibitor’s effect. Similar changes occurred in human stromal cells relevant to menstruation in vitro. Our study provides evidence that PGF2α/PTGFR plays a vital role in endometrial breakdown via vascular changes that are regulated by HIF-1α during menstruation. Graphical Abstract Similar content being viewed by others Data Availability The data supporting the findings of this study are available from the corresponding author upon reasonable request.

References

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Acknowledgements

We would like to express our gratitude to Professor Haibin Wang, Laboratory of Xiamen University, for kindly offering the T-HESCs. The abstract graph was drawn by Figdraw. Funding This work was funded by the National Natural Science Foundation of China (No. 81571410) and the Non-profit Central Research Institute Fund of the National Research Institute for Family Planning (No. 2023GJZD01, 2023GJZ04). Author information Authors and Affiliations Contributions X.X. study supervisor and fund acquisition; F.Z. and W.L. conceived and designed the experiments; F.Z. and S.G. operated the experiments; F.Z., X.C. and C.L. statistical analysis and data visualization; Z.L., X.Z., S.W. and J.W. mouse model assistant; B.H. and T.Z. result interpretation; S.W.4 wrote the manuscript. Corresponding author Ethics declarations Conflict of interest The authors have no conflict of interest to declare. Additional information Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Rights and permissions Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. About this article Cite this article Zhou, F., Wang, S., Lu, W. et al. The Essential Role of PGF2α/PTGFR in Molding Endometrial Breakdown and Vascular Dynamics, Regulated by HIF-1α in a Mouse Menstrual-like Model. Reprod. Sci. 31, 2718–2730 (2024). https://doi.org/10.1007/s43032-024-01526-7 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s43032-024-01526-7

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