Abe K, Shen L S, Takano H
Department of Anatomy, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1991 May;66(3):286-99.
For the basis to study the testicular functions using dd-mice, the cycle of the seminiferous epithelium and stages in spermatogenesis, classification of late spermatogenesis, and postnatal development of spermatogenesis were examined by light and electron microscopy in the testes from these animals at day of birth and 1, 2, 3, 4, 5, and 8 weeks of age. For light microscopy, paraffin sections of the testes were stained with periodic-acid and Schiff reagent (PAS) and hematoxylin. In spermiogenesis, 16 steps of spermatids were distinguished according to shapes of the nuclei and acrosomes. Step 15 and 16 spermatids, which have similar nuclei and acrosomes, were easily distinguishable by positions of nuclei and appearance of basophilic granules in the cytoplasm; steps 15 and 16 were thus subdivided into 3 and 2, respectively. The granules were accumulations of ribosome-like particles. Step 13 spermatids were present with step 1 spermatids, step 14 with steps 2 and 3, step 15 with steps 4-6, and step 16 with steps 7 and 8. Thus, the cycle of the seminiferous epithelium was divided into 12 stages (stages I-XII) in the order of steps 1 to 12. Type A spermatogonia were present in all stages, and intermediate and type B spermatogonia appeared from stages II and VI, respectively. In primary spermatocytes, the resting phase appeared from stage VII, leptotene from stage VIII, zygotene from stage X, pachytene from stage III, diplotene in stage XI, and diakinesis and secondary spermatocytes in stage XII. The seminiferous tubules were lined by Sertoli cells and contained gonocytes at day of birth, type A spermatogonia appeared at 1 week of age, spermatogenesis proceeded until pachytene spermatocytes at 2 weeks, until step 1 spermatids at 3 weeks, and all stages of the seminiferous epithelium were completed at 5 weeks. The findings indicate that combination of germ cells in each stage of the seminiferous epithelium in dd-mice does not correspond to generally accepted one, step 15 and 16 spermatids are accurately classified by referring the position of nuclei and appearance of granules in the cytoplasm, and spermatogenesis in immature mice proceeds faster than in adults.
为了以dd小鼠为基础研究睾丸功能,通过光镜和电镜检查了这些动物出生当天以及1、2、3、4、5和8周龄时睾丸中生精上皮的周期和精子发生阶段、晚期精子发生的分类以及精子发生的出生后发育情况。对于光镜检查,睾丸的石蜡切片用高碘酸和席夫试剂(PAS)以及苏木精染色。在精子形成过程中,根据细胞核和顶体的形状区分出16个精子细胞阶段。第15和16阶段的精子细胞,其细胞核和顶体相似,但可通过细胞核位置和细胞质中嗜碱性颗粒的外观轻松区分;因此,第15和16阶段分别细分为3个和2个亚阶段。这些颗粒是核糖体样颗粒的聚集物。第13阶段的精子细胞与第1阶段的精子细胞同时存在,第14阶段与第2和3阶段同时存在,第15阶段与第4 - 6阶段同时存在,第16阶段与第7和8阶段同时存在。因此,生精上皮的周期按1至12阶段的顺序分为12个阶段(I - XII期)。A型精原细胞存在于所有阶段,中间型和B型精原细胞分别从II期和VI期开始出现。在初级精母细胞中,静止期从VII期开始出现,细线期从VIII期开始,偶线期从X期开始,粗线期从III期开始,双线期在XI期,终变期和次级精母细胞在XII期。生精小管由支持细胞排列,出生时含有生殖母细胞,1周龄时出现A型精原细胞,2周龄时精子发生进展到粗线期精母细胞,3周龄时进展到第1阶段的精子细胞,5周龄时生精上皮的所有阶段完成。这些发现表明,dd小鼠生精上皮各阶段生殖细胞的组合与普遍接受的情况不一致,通过参考细胞核位置和细胞质中颗粒外观可准确分类第15和16阶段的精子细胞,并且未成熟小鼠的精子发生比成年小鼠进展更快。