Baker P J, O'Shaughnessy P J
Division of Veterinary Physiology and Pharmacology, Department of Veterinary Preclinical Studies, University of Glasgow Veterinary School, Bearsden Rd, Glasgow G61 1QH, UK.
Reproduction. 2001 Aug;122(2):227-34. doi: 10.1530/rep.0.1220227.
The role of the gonadotrophins in regulating numbers of Leydig and Sertoli cells during fetal and postnatal development was examined using normal mice and hypogonadal (hpg) mice, which lack circulating gonadotrophins. The disector method was used to determine the number of cells from day 16 of gestation until adulthood. The numbers of Leydig cells did not change significantly between day 16 of gestation and day 5 after parturition in normal mice and were not significantly different from numbers in hpg mice at any age up to day 5 after parturition. There was a 16-fold increase in the number of Leydig cells in normal mice between day 5 and day 20 after parturition, followed by a further doubling of number of cells between day 20 and adulthood. The number of Leydig cells in hpg testes did not change between day 5 and day 20 after parturition but doubled between day 20 and adulthood so that the number of cells was about 10% of normal values from day 20 onwards. Leydig cell volume was constant in normal animals from birth up to day 20 and then showed a 2.5-fold increase in adult animals. Leydig cell volume was normal in hpg testes at birth but decreased thereafter and was about 20% of normal volume in adult mice. The number of Sertoli cells increased continuously from day 16 of gestation to day 20 after gestation in normal mice and then remained static until adulthood. The number of Sertoli cells in hpg testes was normal throughout fetal life but was reduced by about 30% on day 1 (day of parturition). Thereafter, Sertoli cells proliferated at a slower rate but over a longer period in the hpg testis so that on day 20 after parturition the number of Sertoli cells was about 50% of normal values, whereas in adult mice the number was 65% of normal. The number of gonocytes did not change between day 16 of gestation and day 1 and did not differ between normal and hpg testes. The number of gonocytes increased nine-fold in normal testes but only three-fold in hpg testes between day 1 and day 5 after parturition. Gonocytes differentiated into spermatogonia in both normal and hpg testes between day 5 and day 20 after parturition. These results show: (i) that fetal development of both Sertoli and Leydig cells is independent of gonadotrophins; (ii) that normal differentiation and proliferation of the adult Leydig cell population (starting about day 10 after parturition) is dependent on the presence of gonadotrophins; and (iii) that the number of Sertoli cells after birth is regulated by gonadotrophins, although proliferation will continue, at a lower rate and for longer, in the absence of gonadotrophins.
利用正常小鼠和缺乏循环促性腺激素的性腺功能减退(hpg)小鼠,研究了促性腺激素在胎儿期和出生后发育过程中对睾丸间质细胞和支持细胞数量的调节作用。采用分割物镜法确定从妊娠第16天直至成年期的细胞数量。正常小鼠妊娠第16天至产后第5天睾丸间质细胞数量无显著变化,且在产后第5天之前的任何年龄,其数量与hpg小鼠均无显著差异。正常小鼠产后第5天至第20天睾丸间质细胞数量增加了16倍,随后在第20天至成年期细胞数量又增加了一倍。hpg睾丸中,产后第5天至第20天睾丸间质细胞数量无变化,但在第20天至成年期增加了一倍,因此从第20天起细胞数量约为正常值的10%。正常动物出生至第20天,睾丸间质细胞体积保持恒定,成年动物中则增加了2.5倍。hpg睾丸出生时睾丸间质细胞体积正常,但此后减小,成年小鼠中约为正常体积的20%。正常小鼠支持细胞数量从妊娠第16天持续增加至妊娠后第20天,然后保持稳定直至成年。hpg睾丸中支持细胞数量在整个胎儿期均正常,但在出生日(产后第1天)减少了约30%。此后,hpg睾丸中支持细胞增殖速度较慢但持续时间更长,因此产后第20天时支持细胞数量约为正常值的50%,而成年小鼠中该数量为正常值的65%。生殖母细胞数量在妊娠第16天至产后第1天无变化,正常和hpg睾丸之间也无差异。产后第1天至第5天,正常睾丸中生殖母细胞数量增加了9倍,而hpg睾丸中仅增加了3倍。产后第5天至第20天,正常和hpg睾丸中的生殖母细胞均分化为精原细胞。这些结果表明:(i)支持细胞和睾丸间质细胞的胎儿发育均不依赖促性腺激素;(ii)成年睾丸间质细胞群体的正常分化和增殖(约从产后第10天开始)依赖于促性腺激素的存在;(iii)出生后支持细胞数量受促性腺激素调节,尽管在缺乏促性腺激素的情况下,增殖将以较低的速率持续更长时间。