卵丘细胞乙酰辅酶a代谢与母体年龄有关,但与卵母细胞成熟度仅部分相关。

IF 2.1 4区 医学 Q3 ANDROLOGY
Sharon Anderson, Peining Xu, Alexander J Frey, Jason R Goodspeed, Mary T Doan, John J Orris, Nicolle Clements, Michael J Glassner, Nathaniel W Snyder
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引用次数: 0

摘要

卵丘细胞(CC)团块与卵母细胞相关,为卵母细胞提供生长和信号因子。因此,CC的代谢可能影响卵母细胞的功能,而CC的代谢可能预测卵母细胞体外受精的能力。CCs被认为具有高度的糖酵解作用,但缺乏关于人类使用其他潜在碳底物的数据。这项前瞻性和盲法队列研究旨在通过年龄和卵母细胞能力来检查cc的底物利用率。在卵母细胞回收程序后,从参与者身上分离出单独的CC团块,与稳定同位素标记的底物孵育,并使用液相色谱-高分辨率质谱(LC-HRMS)分析主要代谢中间体(包括乙酰辅酶a)的同位素富集。乙酰辅酶a的酰基链含有2个碳,可以从13C标记的底物中得到,从而形成含有2个13C原子的M + 2同位素。比较三种主要碳源的命运,M + 2乙酰辅酶a的平均富集(平均值,标准差)为葡萄糖(3.6,7.7),谷氨酰胺(9.4,6.2)和乙酸(20.7,13.9)。由于这一意想不到的高和可变标记,我们随后检查了来自21名≤34岁女性(49.06,12.73)的278个cc中乙酰辅酶a的平均百分比随着年龄的增长而下降,而来自10名>34岁女性(43.48,16.20)的124个cc中乙酰辅酶a的平均百分比随着年龄的增长而下降(p = 0.0004, t检验)。与中期I和中期II卵母细胞相关的cc相比,未成熟前期I卵母细胞相关的cc中M + 2乙酰辅酶a的富集显著降低(差异:-6.02,CI: -1.74,-13.79, p = 0.013)。单个CC团块的醋酸盐代谢与卵母细胞成熟度呈正相关,随母亲年龄的增加而降低。这些发现表明,非葡萄糖底物的CC代谢应该与卵母细胞功能和年龄相关的生育能力进行研究。缩写词:CCs:积云细胞;COC:卵母细胞复合体;LC-MS:液相色谱-质谱法;乙酰辅酶A:乙酰辅酶A;CoA:辅酶A。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cumulus cell acetyl-CoA metabolism from acetate is associated with maternal age but only partially with oocyte maturity.

Cumulus cell acetyl-CoA metabolism from acetate is associated with maternal age but only partially with oocyte maturity.

Cumulus cell acetyl-CoA metabolism from acetate is associated with maternal age but only partially with oocyte maturity.

Cumulus cell (CC) clumps that associate with oocytes provide the oocytes with growth and signaling factors. Thus, the metabolism of the CCs may influence oocyte function, and CC metabolism may be predictive of oocyte competence for in vitro fertilization. CCs are thought to be highly glycolytic, but data on the use of other potential carbon substrates are lacking in humans. This prospective and blinded cohort study was designed to examine the substrate utilization of CCs by age and oocyte competence. Individual sets of CC clumps from participants were removed after oocyte retrieval procedure then, incubated with stable isotope labeled substrates, and analyzed using liquid chromatography-high resolution mass spectrometry (LC-HRMS) for isotopologue enrichment of major metabolic intermediates, including acetyl-CoA. The acyl-chain of acetyl-CoA contains 2 carbons that can be derived from 13C-labeled substrates resulting in an M + 2 isotopologue that contains 2 13C atoms. Comparing the fate of three major carbon sources, mean enrichment of M + 2 acetyl-CoA (mean, standard deviation) was for glucose (3.6, 7.7), for glutamine (9.4, 6.2), and for acetate (20.7, 13.9). Due to this unexpected high and variable labeling from acetate, we then examined acetyl-CoA mean % enrichment from acetate in 278 CCs from 21 women ≤34 (49.06, 12.73) decreased with age compared to 124 CCs from 10 women >34 (43.48, 16.20) (p = 0.0004, t-test). The CCs associated with the immature prophase I oocytes had significantly lower enrichment in M + 2 acetyl CoA compared to the CCs associated with the metaphase I and metaphase II oocytes (difference: -6.02, CI: -1.74,-13.79, p = 0.013). Acetate metabolism in individual CC clumps was positively correlated with oocyte maturity and decreased with maternal age. These findings indicate that CC metabolism of non-glucose substrates should be investigated relative to oocyte function and age-related fertility.Abbreviations: CCs: cumulus cells; COC: cumulus-oocyte complex; LC-MS: liquid chromatography-mass spectrometry; acetyl-CoA: acetyl-Coenzyme A; CoA: Coenzyme A.

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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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