Leal Marcelo C, Cardoso Edson R, Nóbrega Rafael H, Batlouni Sergio R, Bogerd Jan, França Luiz R, Schulz Rüdiger W
Laboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Biol Reprod. 2009 Jul;81(1):177-87. doi: 10.1095/biolreprod.109.076299. Epub 2009 Apr 1.
The zebrafish has become an important vertebrate model for basic and biomedical research, including the research field of the biology of reproduction. However, very few morphological and stereological data are available regarding zebrafish testis structure and spermatogenesis. In this careful histomorphometric evaluation of the testis, we studied spermatogonial cells using molecular markers, determined the combined duration of meiotic and spermiogenic phases, and examined the formation of the Sertoli cell barrier (tight junctions). We found at least nine spermatogonial generations and propose a morphology-based nomenclature for spermatogonial generations that is compatible with the one used in higher vertebrates. The number of germ cells per cyst increased dramatically (1 to approximately 1360 cells) from undifferentiated spermatogonia type A to early spermatids. The combined duration of meiotic and spermiogenic phases is approximately 6 days, one of the shorter periods among the teleost fish investigated to date. The number of Sertoli cells per cyst increased 9-fold during the maturational cycle of spermatogenic cysts and stabilized in the meiotic phase at a ratio of approximately 100 early spermatids per Sertoli cell (Sertoli cell efficiency). Similarly to mammals, Sertoli cell proliferation ceased in the meiotic phase, coinciding with the formation of tight junctions between Sertoli cells. Hence, the events taking place during puberty in the germinal epithelium of mammals seem to recapitulate the "life history" of each individual spermatogenic cyst in zebrafish.
斑马鱼已成为基础研究和生物医学研究(包括生殖生物学研究领域)的重要脊椎动物模型。然而,关于斑马鱼睾丸结构和精子发生的形态学和体视学数据非常少。在这项对睾丸进行的细致组织形态计量学评估中,我们使用分子标记研究了精原细胞,确定了减数分裂期和精子形成期的总时长,并检测了支持细胞屏障(紧密连接)的形成。我们发现了至少九个精原细胞代,并提出了一种基于形态学的精原细胞代命名法,该命名法与高等脊椎动物中使用的命名法兼容。从未分化的A型精原细胞到早期精子细胞,每个细胞囊中的生殖细胞数量急剧增加(从1个增加到约1360个细胞)。减数分裂期和精子形成期的总时长约为6天,是迄今为止所研究的硬骨鱼中较短的时长之一。在生精细胞囊的成熟周期中,每个细胞囊中的支持细胞数量增加了9倍,并在减数分裂期稳定下来,每个支持细胞对应约100个早期精子细胞的比例(支持细胞效率)。与哺乳动物类似,支持细胞增殖在减数分裂期停止,这与支持细胞之间紧密连接的形成同时发生。因此,哺乳动物生殖上皮在青春期发生的事件似乎概括了斑马鱼中每个生精细胞囊的“生命历程”。