Differential Gene Expression Analysis of Human Ovarian Follicular Cumulus and Mural Granulosa Cells Under the Influence of Insulin in IVF Ovulatory Women and Polycystic Ovary Syndrome Patients Through Network Analysis.

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Endocrine Research Pub Date : 2024-01-02 Epub Date: 2024-01-04 DOI:10.1080/07435800.2023.2272629
Pankaj Pant, Havagiray Chitme, Reema Sircar, Ritu Prasad, Hari Om Prasad
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引用次数: 0

Abstract

Background: Polycystic ovarian syndrome (PCOS) is a commonly occurring reproductive disorder among the reproductive-aged women. Its global occurrence varies based on diagnostic guidelines, ethnicities, and locations of concern. Insulin resistance (IR) is commonly observed around 65-70% of women diagnosed with PCOS, representing a prevalent association. Consequently, the study was designed with an objective of illustrating the effect of insulin on mural and cumulus granulosa cells (GCs) of PCOS patients in comparison to normal ovulating women.

Methodology: This study is a case-control design, wherein a total of 80 participants were recruited meeting criterion of inclusion and exclusion, divided into 8 groups with each group consisting of 10 samples. The process involves the isolation and culturing of mural granulosa cells (MGC) and cumulus granulosa cells (CGC) with and without exposure to insulin. The proteins released by untreated GCs and insulin-treated GCs were extracted, and complex protein mixtures were digested with trypsin, followed by tandem mass spectrometry analysis and data processing using bioinformatics.

Results: We found 595 proteins in both control and PCOS samples, of which 310 were contributed by MGCs and 285 by CGCs. The PCOS MGCs expressed 20%, both the normal MGCs and CGCs have equal representation of 16% by each, whereas the PCOS CGCs proteins contributed 15% of the total of the proteomic expression. However, the poor expression observed with the Insulin exposure, the Insulin treated PCOS CGCs contributes 13%, PCOS MGCs contributes 8%. The normal MGCs upon the Insulin treatment give 8% then and there only 4% of proteins expressed by normal CGCs after Insulin treatment. The Venn analysis widened on their precise expression topographies. The examination of strings exhibited important protein-protein interaction pathways.

Conclusion: This is a pioneering investigation aimed to establish the link between hyperinsulinemia in localized follicular GCs and PCOS mechanisms by comparing them to control group. The examination of various attributes, mechanisms, and traits shown by genes and proteins in individuals with PCOS compared to control populations, alongside the investigation of the dynamics of these genes and proteins following exposure to insulin, holds promise for the formulation of novel hypotheses and strategies in the identification of new biomarkers.

通过网络分析体外受精排卵期妇女和多囊卵巢综合征患者胰岛素对人卵巢卵泡积云和壁粒细胞差异基因表达的影响
背景:多囊卵巢综合征(PCOS)是育龄妇女中常见的生殖障碍。其全球发病率因诊断指南、种族和关注地点而异。胰岛素抵抗(IR)通常在65-70%被诊断为多囊卵巢综合征的女性中观察到,这是一种普遍的关联。因此,本研究旨在说明胰岛素对多囊卵巢综合征患者壁和卵丘颗粒细胞(GC)的影响,与正常排卵女性相比。方法:本研究采用病例对照设计,共招募了80名符合纳入和排除标准的参与者,分为8组,每组10个样本。该过程包括在暴露于胰岛素和不暴露于胰岛素的情况下分离和培养壁颗粒细胞(MGC)和卵丘颗粒细胞(CGC)。提取未处理的GC和胰岛素处理的GC释放的蛋白质,用胰蛋白酶消化复杂的蛋白质混合物,然后使用生物信息学进行串联质谱分析和数据处理。结果:我们在对照和PCOS样本中发现595种蛋白质,其中310种由MGCs贡献,285种由CGCs贡献。PCOS MGCs表达20%,正常MGCs和CGCs各占16%,而PCOS CGCs蛋白占蛋白质组总表达的15%。然而,在胰岛素暴露中观察到的低表达,胰岛素治疗的PCOS CGCs占13%,PCOS MGCs占8%。胰岛素治疗后的正常MGCs产生8%的蛋白质,而胰岛素治疗后正常CGCs仅表达4%的蛋白质。维恩分析扩大了他们精确表达的地形图。对字符串的检查显示出重要的蛋白质-蛋白质相互作用途径。结论:这是一项开创性的研究,旨在通过与对照组的比较,建立局部滤泡性GC的高胰岛素血症与PCOS机制之间的联系。与对照人群相比,对多囊卵巢综合征患者的基因和蛋白质表现出的各种属性、机制和特征的检查,以及对这些基因和蛋白质在暴露于胰岛素后的动力学的研究,有望为鉴定新的生物标志物提出新的假设和策略。
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来源期刊
Endocrine Research
Endocrine Research 医学-内分泌学与代谢
CiteScore
4.30
自引率
0.00%
发文量
10
审稿时长
>12 weeks
期刊介绍: This journal publishes original articles relating to endocrinology in the broadest context. Subjects of interest include: receptors and mechanism of action of hormones, methodological advances in the detection and measurement of hormones; structure and chemical properties of hormones. Invitations to submit Brief Reviews are issued to specific authors by the Editors.
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