Lipke Christian, Meinecke-Tillmann Sabine, Meyer Wilfried, Meinecke Burkhard
Department of Reproductive Biology, University of Veterinary Medicine Hannover Foundation, Buenteweg 2, Hannover 30559, Germany.
Anim Reprod Sci. 2009 Jul;113(1-4):177-86. doi: 10.1016/j.anireprosci.2008.06.005. Epub 2008 Jun 20.
Few ultrastructural studies have been performed on members of the Dendrobatidae, although such investigations can be useful for the understanding of reproductive patterns, as a diagnostic method for males in breeding programs for endangered amphibians and for phylogenetic analysis. The sperm ultrastructure of the Green Poison Frog, Dendrobates auratus, from Panama is described following induced spermiation in living animals. To date only testicular spermatozoa in other dendrobatid frogs have been analysed. Moreover, an electron microscopic preparation method (transmission and scanning electron microscopy) for dendrobatid sperm cells in low concentration is presented. Sperm cells from stimulated frogs (100 IU human chorionic gonadotropin, hCG, twice at an interval of 1h) were recovered via cloaca lavage using 600 microl isotonic phosphate-free amphibian saline (IPS). Centrifuged flushings (5 min, 173 x g) were deposited on microscopic slides. Adherent spermatozoa were treated with Karnovsky fixative (overnight, 4 degrees C). After postfixation (2h, 1% osmium tetroxide), samples were dehydrated in series of ascending acetones (30-100%). For transmission electron microscopy sperm cells were encapsulated using Epon and 1.5% 2,4,6-tris(dimethylaminomethyl)phenol (DMP 30). Ultrathin sections (70 nm) were cut and stained with uranyl acetate (30 min) and lead citrate (5 min). Sperm cells are filiform with a 21.1+/-2.7 microm long and arcuated head and a single tail (35.0+/-4.2 microm length). Their acrosomal complex is located at the anterior portion of the head and consists of the acrosomal vesicle which has low electron density, and the subjacent electron-dense subacrosomal cone. In transverse section, the nucleus is circular (1.9+/-0.2 microm diameter) and conical in longitudinal section. It is surrounded by several groups of mitochondria. The chromatin is highly condensed and electron-dense but shows numerous electron-lucent inclusions. A short midpiece has a mitochondrial collar with a proximal and a distal centriole. The latter gives rise to the axoneme which alone forms the flagellum. The sperm ultrastructure of D. auratus differs from that of other Dendrobatidae because of the absence of a nuclear space and the absence of the undulating membrane associated with an axial fibre. This tail conformation is found in the Ranoidea but not in the Bufonoidea. These results show that the spermatozoa of D. auratus are the first within the Dendrobatidae without accessory tail structures. Methods of using sperm samples from hormonal treated frogs for ultrastructural studies is not only reasonable to examine e.g. amphibian phylogeny without killing frogs threatened with extinction but allows investigations in the field of assisted reproduction and male fertility for example in conservation programs for endangered amphibians.
尽管对箭毒蛙科成员进行超微结构研究有助于理解其繁殖模式、作为濒危两栖动物繁殖计划中雄性的诊断方法以及进行系统发育分析,但此类研究开展得很少。本文描述了来自巴拿马的绿毒蛙(Dendrobates auratus)在活体诱导排精后的精子超微结构。迄今为止,仅对其他箭毒蛙科青蛙的睾丸精子进行过分析。此外,还介绍了一种针对低浓度箭毒蛙科精子细胞的电子显微镜制备方法(透射电子显微镜和扫描电子显微镜)。通过使用600微升等渗无磷酸盐两栖动物生理盐水(IPS)进行泄殖腔灌洗,从经刺激的青蛙(100国际单位人绒毛膜促性腺激素,hCG,间隔1小时注射两次)中回收精子细胞。将离心后的冲洗液(5分钟,转速173×g)置于载玻片上。附着的精子用卡诺夫斯基固定液处理(4℃过夜)。后固定(2小时,1%四氧化锇)后,样品在一系列浓度递增的丙酮(30 - 100%)中脱水。对于透射电子显微镜观察,精子细胞用环氧树脂和1.5% 2,4,6 - 三(二甲氨基甲基)苯酚(DMP 30)包埋。切成超薄切片(70纳米),并用醋酸铀(30分钟)和柠檬酸铅(5分钟)染色。精子细胞呈丝状,头部弯曲,长21.1±2.7微米,有一条单一的尾巴(长35.0±4.2微米)。其顶体复合体位于头部前部,由电子密度低的顶体小泡和下方电子密度高的顶体下圆锥组成。在横切面上,细胞核呈圆形(直径1.9±0.2微米),纵切面上呈圆锥形。它被几组线粒体包围。染色质高度浓缩且电子密度高,但有许多电子透亮的内含物。短的中段有一个线粒体环,有近端和远端中心粒。后者产生轴丝,轴丝单独形成鞭毛。绿毒蛙的精子超微结构与其他箭毒蛙科不同,因为没有核间隙且没有与轴纤维相关的波动膜。这种尾部形态在蛙亚目(Ranoidea)中存在,但在蟾蜍亚目(Bufonoidea)中不存在。这些结果表明,绿毒蛙的精子是箭毒蛙科中首个没有附属尾部结构的。使用经激素处理的青蛙的精子样本进行超微结构研究的方法,不仅对于在不杀死濒危青蛙的情况下研究两栖动物系统发育等是合理的,而且还允许在辅助生殖和雄性生育领域进行研究,例如在濒危两栖动物的保护计划中。