芳香化酶和雌激素受体转录本及其在人类精子中的意义。

Serge Carreau, Galeraud-Denis Isabelle
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引用次数: 11

摘要

人类精子中存在一种复杂的mrna群体,但它们的作用尚未完全阐明。来自可育男性的成熟精子具有潜在的转录能力和/或潜在的从头翻译的证据,有助于理解精子成熟的最后步骤(获能和/或顶体反应)。精子发生受促性腺激素和睾丸激素控制,它们的作用受局部产生的因子调节,其中包括芳香化酶对雄激素的不可逆转化产生的雌激素。数据显示,大鼠生殖细胞中有另一种雌激素来源,同时有几项研究表明,芳香化酶缺乏的男性精子活力下降,这进一步解释了可育男性射精精子中芳香化酶的表达。在静止精子部分中,芳香化酶转录物的数量显著减少。此外,我们还比较了从同一样品制备的低活力精子和高活力精子中编码核浓缩蛋白1和2 (Prm1和Prm2)或能化内皮型一氧化氮合酶(eNOS)、神经元型一氧化氮合酶(nNOS)和c-myc蛋白的转录本水平。c-myc/Prm2比值在两个精子群体间无显著变化。相反,低运动组Prm1 mRNA的表达量显著高于高运动组;在分析的大多数高活动性精子样本中,无法检测到eNOS和nNOS转录本,而在低活动性精子中可以观察到它们。此外,在获能后观察到c-myc转录本部分或完全消失。分析人类射精精子的mRNA谱可以作为评估雄性配子质量的诊断工具和/或作为受精和胚胎发育的预后价值。
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Transcripts of aromatase and estrogen receptors and significance of other RNAs in human spermatozoa.

The existence of a complex population of mRNAs in human sperm is well documented but their role is not completely elucidated. Evidence for a latent transcriptional capacity and/or a potential translation de novo in mature spermatozoa from fertile men has been provided and is helpful in understanding the final steps of sperm maturation (capacitation and/or the acrosome reaction). Spermatogenesis is controlled by gonadotrophins and testosterone, their effects are modulated by locally-produced factors that include estrogens derived from the irreversible transformation of androgens by aromatase. The data demonstrating an additional source of estrogens in rat germ cells along with several studies showing a decreased sperm motility in men deficient in aromatase has led to the further explanation of the expression of aromatase in ejaculated spermatozoa from fertile men. A significant decrease in the amount of aromatase transcripts in the immotile sperm fraction was recorded. In addition, the levels of transcripts encoding for proteins involved in either nuclear condensation protamines 1 and 2 (Prm1 and Prm2) or in capacitation endothelial nitric oxide synthase (eNOS) and neuronal nitric oxide sythase (nNOS) and c-myc were compared in low and high motile sperm prepared from the same sample. No significant change in the ratio of c-myc/Prm2 between the two populations of spermatozoa was observed. Conversely the amount of Prm1 mRNA was significantly higher in the low motile fraction than in the high motile fraction; in most of the high motile sperm samples analyzed, eNOS and nNOS transcripts were undetectable, whereas they were observed in low motile sperm. Moreover, a partial or complete disappearance of c-myc transcripts was observed after capacitation. Analysis of the mRNA profile in human ejaculated sperm could be helpful either as a diagnostic tool to evaluate the male gamete quality and/or as a prognostic value for fertilization and embryo development.

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