Institute of Marine Sciences, Spanish National Research Council (CSIC), 08003 Barcelona, Spain.
Institute of Biotechnology and Biomedicine (IBB), Universitat Autònoma de Barcelona, Bellaterra, Cerdanyola del Vallès, 08193 Barcelona, Spain.
Int J Mol Sci. 2024 Sep 4;25(17):9604. doi: 10.3390/ijms25179604.
Spermatozoon volume regulation is an essential determinant of male fertility competence in mammals and oviparous fishes. In mammals, aquaporin water channels (AQP3, -7 and -8) have been suggested to play a role in spermatozoon cell volume regulatory responses in the hypotonic female oviduct. In contrast, the ejaculated spermatozoa of marine teleosts, such as the gilthead seabream (), experience a high hypertonic shock in seawater, initially resulting in an Aqp1aa-mediated water efflux, cell shrinkage and the activation of motility. Further regulatory recovery of cell volume in post-activated spermatozoa is mediated by Aqp4a in cooperation with the Trpv4 Ca channel and other ion channels and transporters. Using a paralog-specific antibody, here, we show that seabream spermatozoa also express the aquaglyceroporin AQP3 ortholog Aqp3a, which is highly accumulated in the mid posterior region of the spermatozoon flagella, in a similar pattern to that described in mouse and human sperm. To investigate the role of Aqp3a in seabream sperm motility, we used a recently developed AQP3 antagonist (DFP00173), as well as the seabream Aqp3a-specific antibody (α-SaAqp3a), both of which specifically inhibit Aqp3a-mediated water conductance when the channel was heterologously expressed in oocytes. Inhibition with either DFP00173 or α-SaAqp3a did not affect sperm motility activation but did impair the spermatozoon motion kinetics at 30 s post activation in a dose-dependent manner. Interestingly, in close resemblance to the phenotypes of AQP3-deficient murine sperm, electron microscopy image analysis revealed that both Aqp3a inhibitors induce abnormal sperm tail morphologies, including swelling and angulation of the tail, with complete coiling of the flagella in some cases. These findings suggest a conserved role of Aqp3a as an osmosensor that regulates cell volume in fish spermatozoa under a high hypertonic stress, thereby controlling the efflux of water and/or solutes in the post-activated spermatozoon.
精子体积调节是哺乳动物和卵生鱼类雄性生育能力的重要决定因素。在哺乳动物中,水通道蛋白(AQP3、-7 和 -8)被认为在低渗雌性输卵管中精子细胞体积调节反应中发挥作用。相比之下,海洋硬骨鱼(如金头鲷)的射出精子在海水中经历高渗冲击,最初导致 Aqp1aa 介导的水外流、细胞收缩和运动性激活。激活后的精子细胞中细胞体积的进一步调节恢复由 Aqp4a 与 Trpv4 Ca 通道和其他离子通道和转运体合作介导。在这里,我们使用一种同工型特异性抗体表明,金头鲷精子还表达水通道蛋白 aquaglyceroporin AQP3 的直系同源物 Aqp3a,它在精子鞭毛的中后区域高度积累,模式与在小鼠和人类精子中描述的相似。为了研究 Aqp3a 在金头鲷精子运动中的作用,我们使用了一种新开发的 AQP3 拮抗剂(DFP00173)以及金头鲷 Aqp3a 特异性抗体(α-SaAqp3a),当该通道在卵母细胞中异源表达时,这两种抗体都特异性抑制 Aqp3a 介导的水传导。用 DFP00173 或 α-SaAqp3a 抑制均不影响精子运动的激活,但以剂量依赖的方式在激活后 30 秒显著损害精子运动动力学。有趣的是,与 AQP3 缺陷型小鼠精子的表型非常相似,电子显微镜图像分析显示,两种 Aqp3a 抑制剂都诱导精子尾异常形态,包括尾部肿胀和弯曲,在某些情况下鞭毛完全卷曲。这些发现表明 Aqp3a 作为一种渗透压感受器的保守作用,在高渗应激下调节鱼类精子细胞的体积,从而控制激活后精子中水和/或溶质的流出。