Wing T Y, Christensen A K
Am J Anat. 1982 Sep;165(1):13-25. doi: 10.1002/aja.1001650103.
The goal of this morphometric study was to obtain quantitative information on the seminiferous tubules of Sprague-Dawley rats, including changes seen at various stages of the cycle of the seminiferous epithelium. Tissue from perfusion-fixed testes was embedded in Epon-Araldite; and sections were subjected to morphometric measurements at the light microscopic level, using point counting for volume densities and the Floderus equation for numerical densities. Changes occur in the diameter of the seminiferous tubule, as well as in the volume of the seminiferous epithelium and tubule lumen, from stage to stage during the cycle. A significant constriction of the seminiferous tubule accompanies spermiation. The volume of the seminiferous epithelium per unit length of the tubule begins to increase after stage XIV, and peaks at stage V of the next cycle. The tubule lumen increases dramatically from stages V to VII, at the expense of the epithelium. The number of Sertoli cells is constant per unit length of the seminiferous tubule at all stages of the cycle. This is also true for primary spermatocytes of various developmental phases and for round spermatids from step 1 through step 10 of spermiogenesis. The average number of younger (preleptotene, leptotene, zytgotene) primary spermatocytes per Sertoli cell is 2.34 +/- 0.082 (SEM), the number of older (pachytene, diplotene) primary spermatocytes per Sertoli cell is 2.37 +/- 0.064, and the ratio of step 1-10 spermatids to Sertoli cells is 7.89 +/- 0.27. By studying tangential views of serially sectioned seminiferous tubules at stage V, it is shown that the number of step-17 spermatids associated with each Sertoli cell averages 8.35 +/- 0.128, although the counts ranged from 6 to 11. The only appreciable occurrence of cell death after the last spermatogonial mitosis appears to be a 15% loss during the first meiotic division. From our morphometric results, corrected for volume changes during preparation for microscopy, there are 15.7 million (+/- 0.99 million) Sertoli cells per gram of fresh rat testis. The length of seminiferous tubule per gram of testis is estimated to be 12.4 +/- 0.56 meters, and the tubule surface area per gram testis is 119.7 +/- 2.57 cm2. The daily production of mature spermatids is 9.61 million (+/- 0.615 million) per gram of testis.
本形态计量学研究的目的是获取有关Sprague-Dawley大鼠生精小管的定量信息,包括生精上皮周期各阶段所观察到的变化。将灌注固定睾丸的组织包埋于环氧树脂-阿拉迪特中;在光镜水平对切片进行形态计量学测量,采用点计数法计算体积密度,用弗洛德勒斯公式计算数量密度。在生精上皮周期中,生精小管的直径、生精上皮及小管管腔的体积均会逐阶段发生变化。精子释放时,生精小管会出现明显的收缩。每单位长度小管的生精上皮体积在第XIV阶段后开始增加,并在下一周期的第V阶段达到峰值。从第V阶段到第VII阶段,小管管腔显著增大,生精上皮体积相应减小。在生精上皮周期的所有阶段,每单位长度生精小管的支持细胞数量恒定。处于不同发育阶段的初级精母细胞以及精子发生第1步至第10步的圆形精子细胞的数量也保持恒定。每个支持细胞中较年轻(前细线期、细线期、偶线期)初级精母细胞的平均数量为2.34±0.082(标准误),较年长(粗线期、双线期)初级精母细胞的平均数量为2.37±0.064,第1步至第10步精子细胞与支持细胞的比例为7.89±0.27。通过研究第V阶段连续切片生精小管的切线视图发现,每个支持细胞所关联的第17步精子细胞平均数量为8.35±0.128,计数范围为6至11个。在最后一次精原细胞有丝分裂后,唯一明显的细胞死亡现象似乎是在第一次减数分裂期间有15%的细胞损失。根据我们的形态计量学结果,并校正显微镜制备过程中的体积变化,每克新鲜大鼠睾丸中有1570万个(±99万个)支持细胞。每克睾丸中生精小管的长度估计为12.4±0.56米,每克睾丸的小管表面积为119.7±2.57平方厘米。每克睾丸每日产生的成熟精子细胞数量为961万个(±61.5万个)。