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Oocyte-Specific Deletion of Pten Causes Premature Activation of the Primordial Follicle Pool

机译:卵母细胞特定的Pten缺失导致原始卵泡池过早活化

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In the mammalian ovary, progressive activation of primordial follicles from the dormant pool serves as the source of fertilizable ova. Menopause, or the end of female reproductive life, occurs when the primordial follicle pool is exhausted. However, the molecular mechanisms underlying follicle activation are poorly understood. We provide genetic evidence that in mice lacking PTEN (phosphatase and tensin homolog deleted on chromosome 10) in oocytes, a major negative regulator of phosphatidylinositol 3-kinase (PI3K), the entire primordial follicle pool becomes activated. Subsequently, all primordial follicles become depleted in early adulthood, causing premature ovarian failure (POF). Our results show that the mammalian oocyte serves as the headquarters of programming of follicle activation and that the oocyte PTEN-PI3K pathway governs follicle activation through control of initiation of oocyte growth.
机译:在哺乳动物的卵巢中,来自休眠池的原始卵泡的逐步激活是可受精卵的来源。当原始卵泡池耗尽时,就会发生更年期或女性生殖寿命的结束。但是,对卵泡激活的分子机制了解甚少。我们提供的遗传证据表明,在卵母细胞(磷脂酰肌醇3激酶(PI3K)的主要负调节剂)中缺乏PTEN(在10号染色体上缺失的磷酸酶和张力蛋白同源物)的小鼠中,整个原始卵泡池被激活。随后,所有成年卵泡在成年早期都耗尽,导致卵巢早衰(POF)。我们的结果表明,哺乳动物卵母细胞是卵泡活化编程的总部,卵母细胞PTEN-PI3K途径通过控制卵母细胞生长的启动来控制卵泡活化。

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