Department of Veterinary Biosciences, College of Veterinary Medicine, University of Illinois, Urbana-Champaign, Illinois 61802, USA.
Biol Reprod. 2010 May;82(5):958-67. doi: 10.1095/biolreprod.109.080366. Epub 2010 Feb 3.
Estrogen receptor-alpha (ESR1) is highly expressed in the efferent ductules of all species studied as well as in the epididymal epithelium in mice and other select species. Male mice lacking ESR1 (Esr1KO) are infertile, but transplantation studies demonstrated that Esr1KO germ cells are capable of fertilization when placed in a wild-type reproductive tract. These results suggest that extratesticular regions, such as the efferent ductules and epididymis, are the major source of pathological changes in Esr1KO males. Previous studies have shown alterations in ion and fluid transporters in the efferent duct and epididymal epithelia of Esr1KO males, leading to misregulation of luminal fluid pH. To determine the effect of an altered epididymal milieu on Esr1KO sperm, we assayed sperm morphology in the different regions of the epididymis. Sperm recovered from the epididymis exhibited abnormal flagellar coiling and increased incidence of spontaneous acrosome reactions, both of which are consistent with exposure to abnormal epididymal fluid. Analysis of the epididymal fluid revealed that the osmolality of the Esr1KO fluid was reduced relative to wild type, consistent with prior reports of inappropriate fluid absorption from the efferent ductules. This, along with the finding that morphological defects increased with transit through the epididymal duct, suggests that the anomalies in sperm are a consequence of the abnormal luminal environment. Consistent with this, incubating Esr1KO sperm in a more wild-type-like osmotic environment significantly rescued the abnormal flagellar coiling. This work demonstrates that Esr1KO mice exhibit an abnormal fluid environment in the lumen of the efferent ducts and epididymis, precluding normal sperm maturation and instead resulting in progressive deterioration of sperm that contributes to infertility.
雌激素受体-α(ESR1)在所有研究物种的输出小管中以及在小鼠和其他特定物种的附睾上皮中高度表达。缺乏 ESR1(Esr1KO)的雄性小鼠不育,但移植研究表明,当将 Esr1KO 生殖细胞置于野生型生殖道中时,它们能够受精。这些结果表明,睾丸外区域,如输出小管和附睾,是 Esr1KO 男性发生病变的主要来源。先前的研究表明,Esr1KO 雄性的输出小管和附睾上皮中的离子和流体转运蛋白发生改变,导致管腔液体 pH 值失调。为了确定附睾环境改变对 Esr1KO 精子的影响,我们检测了附睾不同区域的精子形态。从附睾中回收的精子表现出鞭毛卷曲异常和自发顶体反应发生率增加,这两者都与暴露于异常附睾液有关。对附睾液的分析表明,Esr1KO 液的渗透压相对于野生型降低,这与先前关于从输出小管不当吸收液体的报道一致。这一点,以及形态缺陷随着通过附睾管的转运而增加的发现,表明精子的异常是由于管腔环境异常所致。与这一发现一致的是,将 Esr1KO 精子在更类似于野生型的渗透环境中孵育可显著挽救异常的鞭毛卷曲。这项工作表明,Esr1KO 小鼠在输出小管和附睾的管腔中表现出异常的液体环境,阻止了正常的精子成熟,反而导致精子逐渐恶化,导致不育。