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From the Cover: Estrogen action and male fertility: Roles of the sodium/hydrogen exchanger-3 and fluid reabsorption in reproductive tract function

机译:从封面开始:雌激素作用和雄性育性:钠/氢交换剂3和液体重吸收在生殖道功能中的作用

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摘要

Estrogen receptor α (ERα) is essential for male fertility. Its activity is responsible for maintaining epithelial cytoarchitecture in efferent ductules and the reabsorption of fluid for concentrating sperm in the head of the epididymis. These discoveries and others have helped to establish estrogen's bisexual role in reproductive importance. Reported here is the molecular mechanism to explain estrogen's role in fluid reabsorption in the male reproductive tract. It is shown that estrogen regulates expression of the Na+/H+ exchanger-3 (NHE3) and the rate of 22Na+ transport, sensitive to an NHE3 inhibitor. Immunohistochemical staining for NHE3, carbonic anhydrase II (CAII), and aquaporin-I (AQP1) was decreased in ERα knockout (αERKO) efferent ductules. Targeted gene-deficient mice were compared with αERKO, and the NHE3 knockout and CAII-deficient mice showed αERKO-like fluid accumulation, but only the NHE3 knockout and αERKO mice were infertile. Northern blot analysis showed decreases in mRNA for NHE3 in αERKO and antiestrogen-treated mice. The changes in AQP1 and CAII in αERKO seemed to be secondary because of the disruption of apical cytoarchitecture. Ductal epithelial ultrastructure was abnormal only in αERKO mice. Thus, in the male, estrogen regulates one of the most important epithelial ion transporters and maintains epithelial morphological differentiation in efferent ductules of the male, independent of its regulation of Na+ transport. Finally, these data raise the possibility of targeting ERα in developing a contraceptive for the male.
机译:雌激素受体α(ERα)对于男性生育至关重要。它的活性负责维持传出小管中的上皮细胞结构,并重吸收液体以浓缩附睾头部的精子。这些发现和其他发现有助于确立雌激素在生殖重要性中的双性恋作用。此处报道的是解释雌激素在男性生殖道中液体吸收中作用的分子机制。结果表明,雌激素调节Na + / H + 交换子3(NHE3)的表达和 22 Na 的比率+ 转运,对NHE3抑制剂敏感。 ERα基因敲除(αERKO)传出小管中NHE3,碳酸酐酶II(CAII)和水通道蛋白-I(AQP1)的免疫组织化学染色降低。将靶向基因缺陷的小鼠与αERKO进行比较,NHE3基因敲除和CAII基因缺陷小鼠表现出类似αERKO的体液积聚,但只有NHE3基因敲除和αERKO小鼠不育。 Northern印迹分析显示αERKO和抗雌激素治疗小鼠中NHE3的mRNA降低。由于顶细胞结构的破坏,αERKO中AQP1和CAII的变化似乎是继发的。导管上皮超微结构仅在αERKO小鼠中异常。因此,在雄性中,雌激素调节最重要的上皮离子转运蛋白之一,并在雄性出射小管中维持上皮形态学分化,而不受Na + 转运的调节。最后,这些数据提高了在男性避孕药中针对ERα的可能性。

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