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Cellular and molecular mechanisms of various types of oocyte aging

机译:各种卵母细胞衰老的细胞和分子机制

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摘要

It is well established that age‐related decline of a womanˈs fertility is related to the poor developmental potential of her gametes. The age‐associated decline in female fertility is largely attributable to the oocyte aging caused by ovarian aging. Age‐associated oocyte aging results in a decrease in oocyte quality. In contrast to ovarian aging, there is a concept of postovulatory oocyte aging. Postovulatory aging of oocytes, not being fertilized for a prolonged time after ovulation, is known to significantly affect the development of oocytes. Both categories of oocyte aging have similar phenotypes of reproductive failure. However, the mechanisms of the decline in oocyte quality are not necessarily equivalent. An age‐dependent increase in aneuploidy is a key determinant of oocyte quality. The reduced expression of molecules regulating cell cycle control during meiosis might be involved in the age‐dependent increase in aneuploidy. The mechanism of age‐associated oocyte aging might be involved in mitochondrial dysfunction, whose etiologies are still unknown. Alternatively, the mechanism of postovulatory oocyte aging might be involved in reactive oxygen species‐induced mitochondrial injury pathways followed by abnormal intracellular Ca2+ regulation of the endoplasmic reticulum. We suggest that future research into the mechanism of oocyte aging will be necessary to develop a method to rescue the poor developmental potential of aged oocytes.
机译:众所周知,与年龄相关的女性生育力下降与配子的发育潜能有关。与年龄相关的女性生育力下降主要归因于卵巢衰老引起的卵母细胞衰老。与年龄相关的卵母细胞衰老导致卵母细胞质量下降。与卵巢衰老相反,有排卵后卵母细胞衰老的概念。卵母细胞的排卵后老化,未在排卵后长时间受精,会显着影响卵母细胞的发育。两种类型的卵母细胞衰老都具有相似的生殖衰竭表型。但是,卵母细胞质量下降的机制不一定是相同的。非整倍体的年龄依赖性增加是卵母细胞质量的关键决定因素。减数分裂过程中调节细胞周期控制分子的表达降低可能与非整倍性的年龄依赖性增加有关。与年龄相关的卵母细胞衰老的机制可能与线粒体功能障碍有关,其病因仍未知。或者,排卵后卵母细胞衰老的机制可能与活性氧诱导的线粒体损伤途径有关,随后是内质网的细胞内Ca 2 + 异常调节。我们建议对卵母细胞衰老的机制进行进一步的研究对于开发一种挽救衰老的卵母细胞发育潜能的方法将是必要的。

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