促性腺激素刺激对卵泡液信号蛋白浓度的影响有限:抗体阵列分析。

International Journal of Reproductive Medicine Pub Date : 2021-01-27 eCollection Date: 2021-01-01 DOI:10.1155/2021/2906164
Nick A Bersinger, Markus Eisenhut, Petra Stute, Michael von Wolff
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引用次数: 1

摘要

目的:卵泡液(FF)在卵泡和卵母细胞的生理活动中起重要作用。促性腺激素刺激会影响FF类固醇激素和抗苗勒管激素(AMH)浓度,这被认为是传统促性腺激素刺激的体外受精(cIVF)中与自然周期体外受精(NC-IVF)相比卵母细胞能力较低的原因。为了分析促性腺激素刺激对广谱信号蛋白的影响,我们对接受NC-IVF和cIVF治疗的妇女的FF进行了蛋白质组抗体阵列检测。方法:20例妇女分别进行一个NC-IVF和一个cIVF治疗周期。第一个抽吸的卵泡液在两组之间使用蛋白质微阵列进行比较,其中包括针对224种与细胞信号和参考蛋白相关的蛋白质的抗体。在进行阵列杂交之前,将40个白蛋白剥离的配对样品中的每一个在反向染色(Cy3/Cy5)程序中进行标记。在专用软件中使用归一化算法进行信号分析。然后在相同的卵泡液中,用ELISA法定量测定5个在阵列实验中P < 0.05的蛋白(胱抑素a、Caspase-3、GAD65/67、ERK-1和ERK-2)。结果:通过未调整的P值,阵列分析仅获得少量差异表达的信号标记。作为多次测定的结果,调整导致阵列上没有任何显著的差异标记表达。用不同来源的抗体对5种未调整的差异表达蛋白进行免疫定量。cIVF的卵泡液胱抑素A和MAP激酶ERK-1浓度显著高于NC-IVF的卵泡,而gad2 (GAD65/67)没有差异。Caspase-3和MAP激酶ERK-2的检测没有要求的敏感性。结论:与FF类固醇激素和AMH相比,促性腺激素刺激不会或仅会轻微改变FF信号蛋白的浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gonadotropin Stimulation Has Only a Limited Effect on the Concentration of Follicular Fluid Signalling Proteins: An Antibody Array Analysis.

Objective: The follicular fluid (FF) plays an essential role in the physiology of the follicle and the oocyte. Gonadotropin stimulation affects the FF steroid hormone and anti-Mullerian hormone (AMH) concentrations, which has been suggested to be the reason for lower oocyte competence in conventional gonadotropin stimulated in vitro fertilisation (cIVF) compared to natural cycle IVF (NC-IVF). To analyse the effect of gonadotropin stimulation on a broad spectrum of signalling proteins, we ran proteomic antibody arrays on FF of women undergoing both treatments NC-IVF and cIVF.

Method: Twenty women underwent one NC-IVF and one cIVF treatment cycle. Follicular fluids of the first aspirated follicle were compared between the two groups using a protein microarray which included antibodies against 224 proteins related to cell signalling and reference proteins. Each of the 40 albumin-stripped, matched-pair samples was labelled in the reverse-dye (Cy3/Cy5) procedure before undergoing array hybridisation. Signal analysis was performed using normalisation algorithms in dedicated software. Five proteins yielding a value of P < 0.05 in the array experiment (Cystatin A, Caspase-3, GAD65/67, ERK-1, and ERK-2) were then submitted to quantitative determination by ELISA in the same follicular fluids.

Results: Array analysis yielded only a small number of differentially expressed signalling markers by unadjusted P values. Adjustment as a consequence of multiple determinations resulted in the absence of any significant differential marker expression on the array. Five unadjusted differentially expressed proteins were quantified immunometrically with antibodies from different sources. Follicular fluid concentrations of Cystatin A and MAP kinase ERK-1 concentrations were significantly higher in the cIVF than in the NC-IVF follicles, while GAD-2 (GAD65/67) did not differ. The assays for Caspase-3 and MAP kinase ERK-2 did not have the required sensitivities.

Conclusion: In contrast to FF steroid hormones and AMH, FF concentrations of signalling proteins are not or only marginally altered by gonadotropin stimulation.

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