Gravis C J
Z Mikrosk Anat Forsch. 1979;93(2):321-42.
The interrelationships of the Sertoli cells and germ cells in the Syrian hamster were examined using the electron microscope. Demosome-like junctions were observed attaching Sertoli cells to spermatogonia and spermatocytes. In the region of the junctions dense plaques lay on the cytoplasmic surfaces of the plasmalemma of the opposing cells. Sertoli cell cytoplasmic filaments converged in the area of the junctions and inserted into the subsurface densities. Filaments were not observed associated with the subsurface densities of the germ cells. In the region of the junctions a 15...20 nm gap, filled with an attenuate amorphous substance, separated the plasmalemmata. Another attachment device termed "junctional specialization" occurred between Sertoli cells, and preleptotene spermatocytes and all successive developmental steps in the germ cell line in the hamster. The junctional specializations consisted of a mantel of Sertoli cell cytoplasmic filament lying subjacent to the Sertoli cell plasmalemma and an opposed cisterna of the endoplasmic reticulum. In stages VII-VIII preleptotene supermatocytes were observed in transit from the basal compartment to the adluminal compartment. While Sertoli-Sertoli junctions adluminal to the spermatocytes remained intact, typical Sertoli-Sertoli junctions formed between opposed Sertoli cell processes basal to the spermatocytes. It is proposed that, during the passage of spermatocytes in to the adluminal compartment, junctional specializations associated with preleptotene spermatocytes in the basal compartment migrate basal to the spermatocytes and contribute to formation of Sertoli-Sertoli junctions. Treatment of seminiferous tubules with hypertonic media was used to demonstrate that the junctional specializations function in cell-to-cell adhesion. Data indicated that these junctions function to retain the developing spermatids within the seminiferous epithelijm until the time of spermiation. At spermination the junctional specializations disappear and the spermatids drift off into the tubule lumen.
利用电子显微镜对叙利亚仓鼠支持细胞与生殖细胞之间的相互关系进行了研究。观察到类似桥粒的连接将支持细胞与精原细胞和精母细胞相连。在连接区域,致密斑位于相对细胞质膜的胞质表面。支持细胞的胞质细丝在连接区域汇聚并插入到亚表面致密物中。未观察到细丝与生殖细胞的亚表面致密物相关联。在连接区域,一个15……20纳米的间隙,充满了稀薄的无定形物质,将质膜分隔开。另一种称为“连接特化”的附着装置出现在支持细胞之间,以及仓鼠生殖细胞系中的前细线期精母细胞和所有后续发育阶段之间。连接特化由位于支持细胞质膜下方的支持细胞胞质细丝套以及相对的内质网池组成。在VII - VIII期,观察到前细线期精母细胞从基底室向近腔室迁移。虽然位于精母细胞上方的支持细胞 - 支持细胞连接保持完整,但在精母细胞下方相对的支持细胞突起之间形成了典型的支持细胞 - 支持细胞连接。有人提出,在精母细胞进入近腔室的过程中,与基底室中的前细线期精母细胞相关的连接特化向精母细胞下方迁移,并有助于支持细胞 - 支持细胞连接的形成。用高渗介质处理生精小管以证明连接特化在细胞间黏附中起作用。数据表明,这些连接的功能是将发育中的精子细胞保留在生精上皮内,直到精子释放时。在精子释放时,连接特化消失,精子细胞漂入小管腔。