Institut de Recerca i Tecnologia Agroalimentàries (IRTA)-Institut de Ciències del Mar, Consejo Superior de Investigaciones Científicas (CSIC), Barcelona, Spain.
Biol Reprod. 2013 Aug 15;89(2):37. doi: 10.1095/biolreprod.113.110783. Print 2013 Aug.
In oviparous vertebrates such as the marine teleost gilthead seabream, water and fluid homeostasis associated with testicular physiology and the external activation of spermatozoa is potentially mediated by multiple aquaporins. To test this hypothesis, we isolated five novel members of the aquaporin superfamily from gilthead seabream and developed paralog-specific antibodies to localize the cellular sites of protein expression in the male reproductive tract. Together with phylogenetic classification, functional characterization of four of the newly isolated paralogs, Aqp0a, -7, -8b, and -9b, demonstrated that they were water permeable, while Aqp8b was also permeable to urea, and Aqp7 and -9b were permeable to glycerol and urea. Immunolocalization experiments indicated that up to seven paralogous aquaporins are differentially expressed in the seabream testis: Aqp0a and -9b in Sertoli and Leydig cells, respectively; Aqp1ab, -7, and -10b from spermatogonia to spermatozoa; and Aqp1aa and -8b in spermatids and sperm. In the efferent duct, only Aqp10b was found in the luminal epithelium. Ejaculated spermatozoa showed a segregated spatial distribution of five aquaporins: Aqp1aa and -7 in the entire flagellum or the head, respectively, and Aqp1ab, -8b, and -10b both in the head and the anterior tail. The combination of immunofluorescence microscopy and biochemical fractionation of spermatozoa indicated that Aqp10b and phosphorylated Aqp1ab are rapidly translocated to the head plasma membrane upon activation, whereas Aqp8b accumulates in the mitochondrion of the spermatozoa. In contrast, Aqp1aa and -7 remained unchanged. These data reveal that aquaporin expression in the teleost testis shares conserved features of the mammalian system, and they suggest that the piscine channels may play different roles in water and solute transport during spermatogenesis, sperm maturation and nutrition, and the initiation and maintenance of sperm motility.
在卵生脊椎动物中,如海洋真鲷,与睾丸生理学和精子的外部激活相关的水和液体稳态可能由多种水通道蛋白介导。为了验证这一假设,我们从真鲷中分离出了水通道蛋白超家族的五个新成员,并开发了同工型特异性抗体,以定位雄性生殖道中蛋白质表达的细胞部位。结合系统发生分类,对新分离的四个同工型(Aqp0a、-7、-8b 和 -9b)的功能特征进行了描述,证明它们是水通透的,而 Aqp8b 也对尿素通透,Aqp7 和 -9b 对甘油和尿素通透。免疫定位实验表明,多达七个同工型的水通道蛋白在真鲷睾丸中差异表达:Aqp0a 和 -9b 分别位于支持细胞和间质细胞中;Aqp1ab、-7 和 -10b 从精原细胞到精子;Aqp1aa 和 -8b 在精细胞和精子中。在输出管中,只有 Aqp10b 存在于腔上皮中。射出的精子显示出五个水通道蛋白的分隔空间分布:Aqp1aa 和 -7 分别位于整个鞭毛或头部,而 Aqp1ab、-8b 和 -10b 都位于头部和前尾。免疫荧光显微镜和精子的生化分级实验表明,Aqp10b 和磷酸化的 Aqp1ab 在激活时迅速转运到头部质膜,而 Aqp8b 积累在精子的线粒体中。相比之下,Aqp1aa 和 -7 保持不变。这些数据表明,硬骨鱼睾丸中的水通道蛋白表达具有哺乳动物系统的保守特征,并且它们表明鱼类通道可能在精子发生、精子成熟和营养、精子运动的启动和维持过程中在水和溶质运输中发挥不同的作用。