Group of Comparative Molecular Physiology, IRTA-Institut de Ciències del Mar, Consejo Superior de Investigaciones Científicas (CSIC), Barcelona, Spain.
Fish Genetics and Reproduction Department, College of Fisheries, Central Agricultural University, Lembucherra, Tripura, India.
J Anat. 2018 Aug;233(2):177-192. doi: 10.1111/joa.12829. Epub 2018 May 27.
Aquaporin-mediated fluid transport in the mammalian efferent duct and epididymis is believed to play a role in sperm maturation and concentration. In fish, such as the marine teleost gilthead seabream (Sparus aurata), the control of fluid homeostasis in the spermatic duct seems also to be crucial for male fertility, but no information exists on the expression and distribution of aquaporins. In this study, reverse transcriptase-polymerase chain reaction and immunoblotting analyses, employing available and newly raised paralog-specific antibodies for seabream aquaporins, indicate that up to nine functional aquaporins, Aqp0a, -1aa, -1ab, -3a, -4a, -7, -8bb, -9b and -10b, are expressed in the spermatic duct. Immunolocalization of the channels in the resting spermatic duct reveals that Aqp0a, -1aa, -4a, -7 and -10b are expressed in the monolayered luminal epithelium, Aqp8b and -9b in smooth muscle fibers, and Aqp1ab and -3a in different interstitial lamina cells. In the epithelial cells, Aqp0a and -1aa are localized in the short apical microvilli, and Aqp4a and -10b show apical and basolateral staining, whereas Aqp7 is solely detected in vesicular compartments. Upon spermiation, an elongation of the epithelial cells sterocilia, as well as the folding of the epithelium, is observed. At this stage, single- and double-immunostaining, using two aquaporin paralogs or the Na /K -ATPase membrane marker, indicate that Aqp1ab, -3a, -7, -8bb and -9b staining remains unchanged, whereas in epithelial cells Aqp1aa translation is supressed, Aqp4a internalizes, and Aqp0a and -10b accumulate in the apical, lateral and basal plasma membrane. These findings uncover a cell type- and region-specific distribution of multiple aquaporins in the piscine spermatic duct, which shares conserved features of the mammalian system. The data therefore suggest that aquaporins may play different roles in the regulation of fluid homeostasis and sperm maturation in the male reproductive tract of fish.
水通道蛋白介导的哺乳动物输出导管和附睾中的液体运输被认为在精子成熟和浓缩中发挥作用。在鱼类中,例如海洋硬骨鱼金头鲷(Sparus aurata),精子导管中的液体动态平衡控制似乎对雄性生育力也至关重要,但关于水通道蛋白的表达和分布尚无信息。在这项研究中,使用现有的和新产生的金头鲷水通道蛋白的同工型特异性抗体,通过逆转录聚合酶链反应和免疫印迹分析表明,多达 9 种功能性水通道蛋白,即 Aqp0a、-1aa、-1ab、-3a、-4a、-7、-8bb、-9b 和 -10b,在精子导管中表达。在静止的精子导管中对通道进行免疫定位显示,Aqp0a、-1aa、-4a、-7 和 -10b 表达在单层腔上皮细胞中,Aqp8b 和 -9b 表达在平滑肌纤维中,Aqp1ab 和 -3a 表达在不同的间质层细胞中。在这些上皮细胞中,Aqp0a 和 -1aa 定位于短的顶微绒毛中,Aqp4a 和 -10b 显示顶侧和基底外侧染色,而 Aqp7 仅在囊泡区室中检测到。在精子发生过程中,上皮细胞 Sterocilia 伸长以及上皮折叠。在这个阶段,使用两种水通道蛋白同工型或 Na+/K+-ATPase 膜标记物进行的单重和双重免疫染色表明,Aqp1ab、-3a、-7、-8bb 和 -9b 的染色保持不变,而在上皮细胞中 Aqp1aa 的翻译被抑制,Aqp4a 内化,Aqp0a 和 -10b 在顶侧、侧面和基底质膜中积累。这些发现揭示了鱼类精子导管中多种水通道蛋白的细胞类型和区域特异性分布,与哺乳动物系统具有保守特征。因此,这些数据表明水通道蛋白可能在鱼类生殖管道中的液体动态平衡和精子成熟的调节中发挥不同的作用。