Suzuki-Toyota Fumie, Ito Chizuru, Toyama Yoshiro, Maekawa Mamiko, Yao Ryoji, Noda Tetsuo, Toshimori Kiyotaka
Department of Anatomy and Developmental Biology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Arch Histol Cytol. 2004 Nov;67(4):361-71. doi: 10.1679/aohc.67.361.
Male mice deleting the gene encoding GOPC (Golgi-associated PDZ- and coiled-coil motif-containing protein) are infertile, showing globozoospermia with a coiled tail (Yao et al., 2002). We confirmed how and where tail anomalies were produced in spermatids and epididymal spermatozoa by light and electron microscopy. During spermiogenesis, tail formation occurred normally, but a defect was found at the posterior ring. Thereafter, remarkable sperm tail deformations were induced during epididymal passage. In the proximal caput epidiymidis, the tails remained normal and straight, but most of them coiled around the nucleus in the cauda epididymidis. Coiling is presumed to occur with the migration of the cytoplasmic droplet by the absence of the posterior ring. The connecting piece of the coiled tail was often dislocated or separated from the implantation fossa. Many mitochondria were separated from the outer dense fibers (ODFs) and formed a stratified mitochondrial sheath. Due to this, the distal part of the midpiece became bared of the mitochondrial sheath. The bared ODFs were often bent and disorganized. Tail deformities are attributed to weak or incomplete adhesion between the following structures: 1) plasma membrane and nuclear envelope at the posterior ring, 2) connecting piece and implantation fossa, and 3) mitochondria and ODFs. These defects result in a coiled tail, tail dislocation from the implantation fossa, and the stratified mitochondrial sheath accompanying bared ODFs in the midpiece, respectively. Thus the posterior ring is significant in preventing coiled tail formation. The GOPC-deficient spermatozoa provide a valuable model not only for head but also for tail anomalies.
缺失编码GOPC(含高尔基体相关PDZ和卷曲螺旋基序蛋白)基因的雄性小鼠不育,表现为圆头精子症并伴有卷曲尾(Yao等人,2002年)。我们通过光学显微镜和电子显微镜确认了精子细胞和附睾精子中尾部异常是如何以及在何处产生的。在精子发生过程中,尾部形成正常,但在后环处发现了缺陷。此后,在附睾运输过程中诱导出明显的精子尾部变形。在附睾头近端,尾部保持正常且笔直,但在附睾尾中大多数尾部围绕细胞核卷曲。据推测,由于后环缺失,细胞质滴迁移导致卷曲发生。卷曲尾的连接段常从植入窝脱位或分离。许多线粒体与外致密纤维(ODF)分离并形成分层的线粒体鞘。因此,中段远端部分没有线粒体鞘。裸露的ODF常常弯曲且紊乱。尾部畸形归因于以下结构之间的粘附力弱或不完全:1)后环处的质膜和核膜,2)连接段和植入窝,3)线粒体和ODF。这些缺陷分别导致卷曲尾、尾部从植入窝脱位以及中段伴有裸露ODF的分层线粒体鞘。因此,后环对于防止卷曲尾形成具有重要意义。GOPC缺陷精子不仅为头部异常,也为尾部异常提供了一个有价值的模型。