Role of the Notch signaling pathway in porcine oocyte maturation.

IF 8.2 2区 生物学 Q1 CELL BIOLOGY Cell Communication and Signaling Pub Date : 2025-01-02 DOI:10.1186/s12964-024-01996-x
Pil-Soo Jeong, Hyo-Gu Kang, Dabin Cha, Se-Been Jeon, Min Ju Kim, Bong-Seok Song, Bo-Woong Sim, Sanghoon Lee
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Abstract

Background: Although the Notch signaling pathway is known to play an important role in ovarian follicle development in mammals, whether it is involved in oocyte maturation remains unclear. Therefore, this study was performed to elucidate the existence and role of the Notch signaling pathway during oocyte maturation in a porcine model.

Methods: Reverse transcription-polymerase chain reaction (RT-PCR) and immunocytochemical assays were used to determine the existence of Notch signaling pathway-related transcripts and proteins in porcine cumulus-oocyte complexes (COCs). In vitro maturation (IVM) and parthenogenetic activation of oocytes were employed to examine the effects of Notch signaling inhibition on meiotic progression and embryogenesis of COCs using RO4929097 (RO), an inhibitor of γ secretase. Various staining methods (TUNEL, Phalloidin-TRITC, MitoTracker, JC-1, BODIPY FL ATP, ER-Tracker, Fluo-3, and Rhod-2) and immunocytochemical and quantitative PCR assays were used to identify the effects of Notch signaling inhibition on meiotic progression, embryogenesis, cell cycle progression, spindle assembly, chromosome alignment, mitochondrial and endoplasmic reticulum distribution, and downstream pathway targets in COCs.

Results: The RT-PCR and immunocytochemical analyses revealed the presence of Notch signaling-related receptors (NOTCH1-4) and ligands (JAG1 and 2 and DLL1, 3, and 4) at 0, 22, 28, and 44 h of IVM in the COCs. RO treatment during oocyte maturation markedly reduced meiotic maturation and embryogenesis, inhibiting the cell cycle progression, spindle assembly, and chromosome alignment processes that are important for meiotic maturation. Furthermore, RO significantly impaired the cellular distribution and functions of the mitochondria and endoplasmic reticula, which are important organelles for the cytoplasmic maturation of oocytes. Finally, the involvement of canonical Notch signaling in oocyte maturation was confirmed by the decreased expression of HES and HEY family transcripts and proteins in the RO-treated COCs.

Conclusions: It was first demonstrated that Notch signaling pathway-related transcripts and proteins were expressed during the meiotic maturation of porcine COCs. Furthermore, the inhibition of Notch signaling during IVM revealed the essential role of this signaling pathway during oocyte maturation in pigs.

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Notch信号通路在猪卵母细胞成熟中的作用。
背景:虽然Notch信号通路在哺乳动物卵泡发育中起重要作用,但其是否参与卵母细胞成熟尚不清楚。因此,本研究旨在阐明Notch信号通路在猪卵母细胞成熟过程中的存在及其作用。方法:采用逆转录聚合酶链反应(RT-PCR)和免疫细胞化学方法检测猪卵母细胞复合体(COCs)中Notch信号通路相关转录物和蛋白的存在。利用γ分泌酶抑制剂RO4929097 (RO),通过体外成熟(IVM)和卵母细胞孤雌活化研究Notch信号抑制对COCs减数分裂进程和胚胎发生的影响。采用多种染色方法(TUNEL、Phalloidin-TRITC、MitoTracker、JC-1、BODIPY FL ATP、ER-Tracker、Fluo-3和Rhod-2)、免疫细胞化学和定量PCR方法鉴定Notch信号抑制对COCs减数分裂进程、胚胎发生、细胞周期进程、纺锤体组装、染色体排列、线粒体和内质网分布以及下游途径靶点的影响。结果:RT-PCR和免疫细胞化学分析显示,在IVM的0、22、28和44 h, COCs中存在Notch信号相关受体(NOTCH1-4)和配体(JAG1和2以及DLL1、3和4)。在卵母细胞成熟过程中,RO处理显著降低了减数分裂成熟和胚胎发生,抑制了细胞周期进程、纺锤体组装和染色体对齐过程,这些过程对减数分裂成熟很重要。此外,RO显著损害了线粒体和内质网的细胞分布和功能,而线粒体和内质网是卵母细胞细胞质成熟的重要细胞器。最后,在ro处理的COCs中,HES和HEY家族转录本和蛋白的表达减少,证实了Notch信号在卵母细胞成熟过程中的参与。结论:首次证实Notch信号通路相关转录物和蛋白在猪COCs减数分裂成熟过程中表达。此外,IVM过程中Notch信号通路的抑制揭示了该信号通路在猪卵母细胞成熟过程中的重要作用。
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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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