Marshall G R, Plant T M
Department of Pediatrics, University of Pittsburgh, School of Medicine, Pennsylvania 15261, USA.
Biol Reprod. 1996 Jun;54(6):1192-9. doi: 10.1095/biolreprod54.6.1192.
The pubertal ontogeny of Sertoli cell proliferation in primates is controversial. In the study of the rhesus monkey presented here, we investigated this issue during normal sexual maturation and during precocious puberty induced experimentally with pulsatile GnRH treatment. Cell number was calculated by standard stereological methods employing volume fraction of either seminiferous tubule or, whenever possible, cell nuclei. In the first experiment, testes were collected from normal monkeys at three developmental phases: neonates (7-18 days old, n = 5); juveniles (approximately 17 mo old, n = 4); and adults (5 yr and older, n = 4). In the second experiment, tissue was obtained from an additional three untreated juvenile monkeys and from six other juveniles of comparable age that had been subjected to premature activation of the pituitary-testicular axis for 5 or 10 wk with pulsatile GnRH (1 microgram/min for 3 min every 3 h). The number of Sertoli cells in adults was 6-fold greater than that in neonatal and juvenile animals. A similar increase in number of this somatic cell type was also observed during experimentally induced puberty. A less dramatic proliferation of Sertoli cells occurred during the neonatal-juvenile transition. Although the increase in Sertoli cell number between the juvenile and adult stages of development was paralleled by a comparable change in Ad and Ap spermatogonia, proliferation of these stem spermatogonia during premature activation of the pituitary-testicular axis was less striking. These results lead to the suggestion that, in primates, the onset of puberty is associated with a rapid and substantial proliferation of Sertoli cells, which is subsequently followed by amplification of stem spermatogonia. They also indicate that while Sertoli cells and stem spermatogonia proliferate during infancy and juvenile development, these earlier changes appear to be more insidious than those at puberty.
灵长类动物支持细胞增殖的青春期个体发育过程存在争议。在本文所呈现的恒河猴研究中,我们在正常性成熟过程以及通过脉冲式GnRH治疗实验诱导的性早熟过程中对这一问题进行了研究。细胞数量通过标准的体视学方法计算,该方法采用生精小管的体积分数,或者在可能的情况下采用细胞核的体积分数。在第一个实验中,从处于三个发育阶段的正常猴子身上采集睾丸:新生儿(7 - 18日龄,n = 5);幼年猴(约17个月龄,n = 4);以及成年猴(5岁及以上,n = 4)。在第二个实验中,从另外三只未经治疗的幼年猴子以及六只年龄相仿但已通过每3小时一次、每次3分钟、剂量为1微克/分钟的脉冲式GnRH使垂体 - 睾丸轴提前激活5周或10周的幼年猴子身上获取组织。成年猴的支持细胞数量比新生猴和幼年动物多6倍。在实验诱导的青春期期间也观察到了这种体细胞类型数量的类似增加。在新生儿 - 幼年过渡阶段,支持细胞的增殖不太显著。尽管在幼年和成年发育阶段之间支持细胞数量的增加与Ad和Ap精原细胞的类似变化平行,但在垂体 - 睾丸轴提前激活期间,这些精原干细胞的增殖并不那么明显。这些结果表明,在灵长类动物中,青春期的开始与支持细胞的快速大量增殖相关,随后是精原干细胞的扩增。它们还表明,虽然支持细胞和精原干细胞在婴儿期和幼年发育期间会增殖,但这些早期变化似乎比青春期的变化更为隐匿。