França Luiz R, Godinho Christiane L
Laboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil 31270-901.
Biol Reprod. 2003 May;68(5):1554-61. doi: 10.1095/biolreprod.102.010652. Epub 2002 Nov 27.
There is very little information regarding the testis structure and function in domestic cats, mainly data related to the cycle of seminiferous epithelium and sperm production. The testis weight in cats investigated in the present study was 1.2 g. Compared with most mammalian species investigated, the value of 0.08% found for testes mass related to the body mass (gonadosomatic index) in cats is very low. The tunica albuginea volume density (%) in these animals was relatively high and comprised about 19% of the testis. Seminiferous tubule and Leydig cell volume density (%) in cats were approximately 90% and 6%, respectively. The mean tubular diameter was 220 microm, and 23 m of seminiferous tubule were found per testis and per gram of testis. The frequencies of the eight stages of the cycle, characterized according to the tubular morphology system, were as follows: stage 1, 24.9%; stage 2, 12.9%; stage 3, 7.7%; stage 4, 17.6%; stage 5, 7.2%; stage 6, 11.9%; stage 7, 6.8%; and stage 8, 11 %. The premeiotic and postmeiotic stage frequency was 46% and 37%, respectively. The duration of each cycle of seminiferous epithelium was 10.4 days and the total duration of spermatogenesis based on 4.5 cycles was 46.8 days. The number of round spermatids for each pachytene primary spermatocytes (meiotic index) was 2.8, meaning that significant cell loss (30%) occurred during the two meiotic divisions. The total number of germ cells and the number of round spermatids per each Sertoli cell nucleolus at stage 1 of the cycle were 9.8 and 5.1, respectively. The Leydig cell volume was approximately 2000 microm3 and the nucleus volume 260 microm3. Both Leydig and Sertoli cell numbers per gram of testis in cats were approximately 30 million. The daily sperm production per gram of testis in cats (efficiency of spermatogenesis) was approximately 16 million. To our knowledge, this is the first investigation to perform a more detailed and comprehensive study of the testis structure and function in domestic cats. Also, this is the first report in the literature showing Sertoli and Leydig cell number per gram of testis and the daily sperm production in any kind of feline species. In this regard, besides providing a background for comparative studies with other fields, the data obtained in the present work might be useful in future studies in which the domestic cat could be utilized as an appropriate receptor model for preservation of genetic stock from rare or endangered wild felines using the germ cell transplantation technique.
关于家猫睾丸结构和功能的信息非常少,主要是与生精上皮周期和精子产生相关的数据。本研究中所调查的猫的睾丸重量为1.2克。与所研究的大多数哺乳动物物种相比,猫的睾丸质量与体重的比值(性腺指数)为0.08%,该值非常低。这些动物的白膜体积密度(%)相对较高,约占睾丸的19%。猫的生精小管和间质细胞体积密度(%)分别约为90%和6%。生精小管的平均直径为220微米,每个睾丸及每克睾丸中的生精小管长度为23米。根据生精小管形态系统划分的生精周期八个阶段的频率如下:第1阶段,24.9%;第2阶段,12.9%;第3阶段,7.7%;第4阶段,17.6%;第5阶段,7.2%;第6阶段,11.9%;第7阶段,6.8%;第8阶段,11%。减数分裂前期和减数分裂后期的阶段频率分别为46%和37%。生精上皮每个周期的持续时间为10.4天,基于4.5个周期的精子发生总持续时间为46.8天。每个粗线期初级精母细胞产生的圆形精子细胞数量(减数分裂指数)为2.8,这意味着在两次减数分裂过程中发生了显著的细胞损失(30%)。在周期第1阶段,每个支持细胞核仁中的生殖细胞总数和圆形精子细胞数量分别为9.8和5.1。间质细胞体积约为2000立方微米,细胞核体积为260立方微米。猫每克睾丸中的间质细胞和支持细胞数量均约为3000万个。猫每克睾丸的每日精子产量(精子发生效率)约为1600万个。据我们所知,这是首次对家猫睾丸结构和功能进行更详细、全面研究的调查。此外,这也是文献中首次报道任何猫科动物每克睾丸中的支持细胞和间质细胞数量以及每日精子产量。在这方面,除了为与其他领域的比较研究提供背景外,本研究获得的数据可能对未来的研究有用,在未来研究中,家猫可作为合适的受体模型,利用生殖细胞移植技术保存珍稀或濒危野生猫科动物的遗传种质。