HDAC3在排卵颗粒细胞异常表达诱导卵母细胞成熟障碍的致病机制及其在IVM中的应用。

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biological Chemistry Pub Date : 2025-03-01 Epub Date: 2025-02-10 DOI:10.1016/j.jbc.2025.108287
Huarong Wang, Han Cai, Meiling Zhang, Chuanhui Guo, Peike Wang, Na Deng, Haili Bao, Fanjing Meng, Qing Li, Shuiying Ma, Shuangbo Kong, Wenbo Deng, Hua Zhang, Guoliang Xia, Fengchao Wang, Chao Wang, Haibin Wang
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引用次数: 0

摘要

卵母细胞成熟障碍困扰着女性生殖健康。在哺乳动物中,颗粒细胞(GCs)介导黄体生成素对卵母细胞成熟和排卵的作用。然而,对卵母细胞成熟阻滞中GCs紊乱的发病机制研究甚少。我们前期的研究表明,生理性状态下,LH降低了GCs中的HDAC3。在这里,我们观察到与正常卵母细胞成熟的患者相比,黄体生成素治疗后卵母细胞成熟障碍患者的GCs中HDAC3水平显著升高。为了弄清排卵期GCs中异常高水平的HDAC3是否会导致雌性不育,我们构建了小鼠gc条件下HDAC3过表达模型。结果显示,排卵期GCs中异常高水平的HDAC3抑制了LH对卵母细胞成熟和排卵的诱导,导致女性不育。此外,在HDAC3水平异常高的GCs中,hac3通过降低启动子区域的H3K14ac水平,减弱了LH诱导的卵母细胞成熟相关基因的上调,这表明hac3在GCs中的作用在很大程度上受到hac3的负向控制。应用HDAC3抑制剂增强临床患者GCs中与卵母细胞成熟相关的多个基因的表达,最终提高卵母细胞成熟率和发育质量,表现为更高的囊胚发育率。这些发现有助于丰富对其病理机制的认识,并为卵母细胞成熟障碍患者提供最佳的治疗策略。
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Pathogenic mechanism of abnormal expression of HDAC3 in ovulatory granulosa cells inducing oocyte maturation disorder and its application in IVM.

Female reproductive health is troubled by oocyte maturation disorder. In mammals, granulosa cells (GCs) mediate luteinizing hormone (LH) action on oocyte maturation and ovulation. However, the pathogenesis of disordered GCs in oocyte maturation arrest is rarely studied. Our previous study has showed that HDAC3 (histone deacetylase 3) in GCs was decreased by LH at physiological conditions. Here, we observed significantly elevated HDAC3 levels in GCs from patients with oocyte maturation disorder following LH treatment compared with those with normal oocyte maturation. To clarify whether abnormally high levels of HDAC3 in ovulatory GCs resulted in female infertility, a mice model of GC-conditional overexpression of Hdac3 was constructed. The results showed that abnormally high levels of HDAC3 in ovulatory GCs inhibited LH induction on oocyte maturation and ovulation, resulting in female infertility. Further, in GCs with abnormal high levels of HDAC3, the upregulation of oocyte maturation-related genes induced by LH was attenuated by HDAC3 through a reduction in H3K14ac levels in the promoter regions, implying that the action of LH in GCs was largely negatively controlled by HDAC3. Applying HDAC3 inhibitors enhanced the expression of multiple genes associated with oocyte maturation in GCs from clinical patients, ultimately improving both the oocyte maturation rate and developmental quality, as demonstrated by a higher blastocyst development rate. The findings contribute to both enrich understanding upon the pathological mechanisms and supply optimal treatment strategies for patients with oocyte maturation disorder.

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Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
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期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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