The Thromboxane Levels in Ovarian Follicular Fluid Are Inversely Correlated With Oocyte Maturation: Implications of PAR-2/-3 Cooperation and Thromboxane Participation in Follicle Development
{"title":"The Thromboxane Levels in Ovarian Follicular Fluid Are Inversely Correlated With Oocyte Maturation: Implications of PAR-2/-3 Cooperation and Thromboxane Participation in Follicle Development","authors":"Hsuan-Ting Chen, Tsung-Hsuan Lai, Jun-Jie Lin, Chao-Chi Chen, Wen-Bin Wu","doi":"10.1002/jcp.70025","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>It has been reported the presence of components from the coagulation thrombin-generating pathway and prostaglandins (PGs) in human ovarian follicular fluid (FF) but with unclear functions. Moreover, thrombin can induce COX-2 expression linking to PG synthesis in several cell types. Therefore, this study sought to explore the thromboxane (TX) generation in FF and the correlation between FF TX levels and oocyte maturation. The FF TXB<sub>2</sub> (a stable metabolite of TXA<sub>2</sub>) levels exhibited a negative correlation between large preovulatory leading and small mid-antral follicles from in vitro fertilization (IVF) patients, indicating a requirement of TX for a small follicle/oocyte to grow/mature. Further receiver operating characteristic curve analysis identified that intrafollicular TXB<sub>2</sub> level could predict oocyte maturity. Thrombin was found expressed in a similar pattern/trend to TXB<sub>2</sub> in intrafolliclar FF, where it could induce TXB<sub>2</sub> production/secretion in human ovarian follicular GCs via proteinase-activated receptor-2 (PAR-2) and PAR-3 cooperation/transactivation and Erk/p38 MAPK/JNK signaling to cause COX-2/TXB<sub>2</sub> induction. Accordingly, PAR-2 and -3 were present in human ovarian follicular GCs and thrombin, PAR-2 agonist, and TXA<sub>2</sub> analog caused a substantial enhancement in follicle development, which could be blocked by the PAR-2, COX-2, and TXA<sub>2</sub> prostanoid (TP) receptor inhibitors in an ex vivo cultured murine ovary model. Collectively, we first demonstrated that FF thrombin regulates PAR-2/-3 cooperation and MAPK signaling pathways to induce COX-2 expression and TX production in follicular GCs, possibly supporting intrafollicular TX levels and triggering TP-related pathways to enhance follicle development. The FF TX levels also can be a predictor for oocyte maturation during IVF.</p>\n </div>","PeriodicalId":15220,"journal":{"name":"Journal of Cellular Physiology","volume":"240 4","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cellular Physiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jcp.70025","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
It has been reported the presence of components from the coagulation thrombin-generating pathway and prostaglandins (PGs) in human ovarian follicular fluid (FF) but with unclear functions. Moreover, thrombin can induce COX-2 expression linking to PG synthesis in several cell types. Therefore, this study sought to explore the thromboxane (TX) generation in FF and the correlation between FF TX levels and oocyte maturation. The FF TXB2 (a stable metabolite of TXA2) levels exhibited a negative correlation between large preovulatory leading and small mid-antral follicles from in vitro fertilization (IVF) patients, indicating a requirement of TX for a small follicle/oocyte to grow/mature. Further receiver operating characteristic curve analysis identified that intrafollicular TXB2 level could predict oocyte maturity. Thrombin was found expressed in a similar pattern/trend to TXB2 in intrafolliclar FF, where it could induce TXB2 production/secretion in human ovarian follicular GCs via proteinase-activated receptor-2 (PAR-2) and PAR-3 cooperation/transactivation and Erk/p38 MAPK/JNK signaling to cause COX-2/TXB2 induction. Accordingly, PAR-2 and -3 were present in human ovarian follicular GCs and thrombin, PAR-2 agonist, and TXA2 analog caused a substantial enhancement in follicle development, which could be blocked by the PAR-2, COX-2, and TXA2 prostanoid (TP) receptor inhibitors in an ex vivo cultured murine ovary model. Collectively, we first demonstrated that FF thrombin regulates PAR-2/-3 cooperation and MAPK signaling pathways to induce COX-2 expression and TX production in follicular GCs, possibly supporting intrafollicular TX levels and triggering TP-related pathways to enhance follicle development. The FF TX levels also can be a predictor for oocyte maturation during IVF.
期刊介绍:
The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.