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Granulosa cell biomarkers to predict oocyte and embryo quality in assisted reproductive technology

机译:甘蓝粒细胞生物标志物预测辅助生殖技术中的卵母细胞和胚胎质量

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With the development of human assisted reproductive technology (ART), an objective, accurate, and non-invasive method to assess the quality and viability of oocytes and embryos remains one of the most significant goals. Granulosa cells (GCs) play an essential role in oocyte development. GCs can differentiate into mural GCs (MGCs) and cumulus cells (CCs) under the influence of oocytes. MGCs promote the growth and development of follicles by secreting cytokines and steroid hormones. Simultaneously, CCs can form cumulus-oocyte complexes to communicate with oocytes through gap junctions and promote oocyte growth and maturation. Seeking suitable biomarkers in GCs provides a direction for the non-invasive assessment of oocyte and embryo abilities during ART procedures. To date, only a few studies have investigated potentially effective GC biomarkers during ART processes, such as the apoptosis of GCs, transcriptomic characteristics of GCs, quality and quantity of mitochondria in GCs, and telomere length of such cells. These are potential reference indices for screening high-quality oocytes and embryos. Independent studies on MGCs and CCs can provide more effective results. Although there is scope for optimization and improvement, the results have become increasingly accurate with the constant advances in technology. Due to the heterogeneity of the study population and technical limitations, clinical tests for GCs cannot be performed as part of routine tests, but their prospects are promising. This article reviews the biomarkers that have been studied in MGCs and CCs.
机译:随着人类辅助生殖技术(艺术品)的发展,客观,准确和非侵入性方法,以评估卵母细胞和胚胎的质量和活力仍然是最重要的目标之一。甘蓝细胞(GCS)在卵母细胞发育中起重要作用。 GCS可以在卵母细胞的影响下分化为壁龛GCS(MGCs)和积分菌细胞(CCS)。 MGCS通过分泌细胞因子和类固醇激素来促进卵泡的生长和开发。同时,CCS可以通过间隙结合形成卵母细胞复合物,以通过间隙结与卵母细胞连通,并促进卵母细胞生长和成熟。在GCS中寻求合适的生物标志物为在艺术程序期间提供了对卵母细胞和胚胎能力的非侵入性评估的方向。迄今为止,只有少数研究在艺术过程中调查了潜在有效的GC生物标志物,例如GCS的凋亡,GCS转录组特征,GCS中线粒体的质量和数量,以及这种细胞的端粒长度。这些是用于筛选高质量卵母细胞和胚胎的潜在参考指标。对MGCS和CCS的独立研究可以提供更有效的结果。虽然有优化和改进的范围,但技术不断进步,结果越来越准确。由于研究人口的异质性和技术限制,GCS的临床试验不能作为常规测试的一部分进行,但它们的前景是有前途的。本文审查了在MGCS和CCS中研究的生物标志物。

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