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首页> 外文期刊>Steroids: An International Journal >Progestin functions in vertebrate gametes mediated by membrane progestin receptors (mPRs): Identification of mPRalpha on human sperm and its association with sperm motility.
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Progestin functions in vertebrate gametes mediated by membrane progestin receptors (mPRs): Identification of mPRalpha on human sperm and its association with sperm motility.

机译:膜孕激素受体(mPRs)介导的脊椎动物配子中的孕激素功能:鉴定人类精子上的mPRalpha及其与精子运动性的关系。

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Most of the studies on the putative membrane progestin receptor (mPR) alpha and beta subtypes that have been published in the 5 years since their discovery have supported the original hypothesis that they function as specific membrane receptors through which progestins induce rapid, nongenomic responses in target cells. Recent evidence that mPRalpha and mPRbeta have important roles in the regulation of oocyte meiotic maturation and sperm motility in both fish and mammals is reviewed. Although rapid, cell surface-initiated progestin actions on sperm to induce hyperactive motility have been demonstrated in several mammalian models, the identity of the membrane progestin receptor mediating this effect remains unclear. We demonstrate here that mPRalpha mRNA is expressed in human sperm by RT-PCR and that the mPRalpha protein is localized to the sperm membranes by Western blot analysis. Immunocytochemical staining of whole non-permeabilized human sperm confirmed the mPRalpha protein is expressed in the plasma membrane, and showed it is localized to the sperm midpiece, indicating a likely role of mPRalpha in progestin regulation of sperm motility. Moreover, the abundance of the mPRalpha protein on sperm plasma membranes from human donors that displayed low motility was significantly reduced compared to that on normal motile sperm. Finally, progestin treatment of sperm membranes caused activation of G-proteins. These results suggest that, similar to its proposed function in fishes, mPRalpha is an intermediary in progestin stimulation of sperm motility in humans by a mechanism involving G-protein activation.
机译:自发现以来的5年间,有关推定膜孕激素受体(mPR)α和β亚型的大多数研究都支持最初的假设,即它们起特定膜受体的作用,孕激素通过这些受体诱导靶标快速,非基因组反应细胞。最近的证据表明,mPRalpha和mPRbeta在鱼类和哺乳动物的卵母细胞减数分裂成熟和精子运动的调节中起着重要作用。尽管在几种哺乳动物模型中已经证明了细胞表面引发的孕激素对精子的快速反应以诱导过度活跃的运动,但是介导这种作用的膜孕激素受体的身份仍然不清楚。我们在这里证明了mPRalpha mRNA在人的精子中通过RT-PCR表达,并且mPRalpha蛋白通过Western blot分析定位在精子膜上。整个未透化的人类精子的免疫细胞化学染色证实了mPRalpha蛋白在质膜中表达,并表明它位于精子中段,表明mPRalpha在孕激素调节精子活力中可能发挥作用。而且,与正常的运动精子相比,运动能力低的人类供体的精子质膜上的mPRalpha蛋白丰度大大降低。最后,孕激素对精子膜的处理引起了G蛋白的活化。这些结果表明,与拟议中的鱼类功能相似,mPRalpha是孕激素通过涉及G蛋白活化的机制刺激人类精子运动的中介。

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