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

IF 4.5 2区 生物学 Q2 CELL BIOLOGY
Hsuan-Ting Chen, Tsung-Hsuan Lai, Jun-Jie Lin, Chao-Chi Chen, Wen-Bin Wu
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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.

卵巢卵泡液中血栓素水平与卵母细胞成熟呈负相关:PAR-2/ 3合作和血栓素参与卵泡发育的意义
据报道,人卵巢卵泡液(FF)中存在凝血凝血酶生成途径和前列腺素(pg)成分,但功能不明确。此外,凝血酶可以诱导几种细胞类型中与PG合成相关的COX-2表达。因此,本研究旨在探讨FF中血栓素(txx)的产生以及FF txx水平与卵母细胞成熟的相关性。体外受精(IVF)患者的fftxb2 (TXA2的稳定代谢物)水平在排卵期前导大卵泡和中腔小卵泡之间呈负相关,表明小卵泡/卵母细胞生长/成熟需要TXB2。进一步的受者工作特征曲线分析发现,卵泡内TXB2水平可以预测卵母细胞成熟度。凝血酶在卵泡内FF中的表达模式与TXB2相似,通过蛋白酶激活受体-2 (PAR-2)和PAR-3的协同/转激活以及Erk/p38 MAPK/JNK信号通路诱导COX-2/TXB2在人卵巢卵泡GCs中产生/分泌。因此,PAR-2和-3存在于人卵巢卵泡GCs中,凝血酶、PAR-2激动剂和TXA2类似物可显著促进卵泡发育,而在体外培养的小鼠卵巢模型中,PAR-2、COX-2和TXA2前列腺素(TP)受体抑制剂可阻断这一作用。总的来说,我们首先证明了FF凝血酶调节PAR-2/ 3合作和MAPK信号通路,诱导卵泡GCs中COX-2的表达和TX的产生,可能支持滤泡内TX水平并触发tp相关通路,以促进卵泡发育。FF TX水平也可以作为体外受精过程中卵母细胞成熟的预测指标。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
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.
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