Yeung C H, Cooper T G
Cell Tissue Res. 1982;226(2):407-25. doi: 10.1007/BF00218369.
The appearance of the rat epididymal epithelium changed when it was perfused in vivo through the lumen with unphysiologically high sodium ion concentrations; dilatation of intercellular spaces (ICS) at threshold concentrations of 30 mM-Na+ in the cauda and about 55 mM-Na+ in the corpus was associated with absorption of water from the lumen. Despite the distended ICS, junctional complexes appeared intact, and their integrity was confirmed by the exclusion of luminal horseradish peroxidase (HRP) from the ICS, and by demonstrating that circulating [3H]inulin did not enter the lumen. Smooth ER and lipid droplets in the principal cells of the corpus epididymidis were well maintained, and the preservation of granular ER in principal cells of the cauda epididymidis lent morphological support to the continued secretion of protein in this segment. However, occasional distension or involution of inner Golgi cisternae was evident in principal cells after 3-6 h perfusion. In contrast to multivesicular bodies of principal cells, the apical and basal vacuoles characteristic of clear cells changed in size with different perfusion. In contrast to multivesicular bodies of principal cells, the apical and basal vacuoles characteristic of clear cells changed in size with different perfusing solutions. When low Na+ concentrations were perfused large translucent vacuoles were frequently found in the apical cytoplasm of clear cells in the corpus and cauda epididymidis, and filled vacuoles became larger and showed a decrease in content density in the cauda epididymidis. These large vacuoles were absent from tissue perfused with high Na+ concentrations. Normal pinocytotic activity of both cell types was demonstrated by perfusing HRP which was taken up by the normal route in principal cells, with some transfer to the Golgi cisternae. By far the most HRP was accumulated in clear cell vacuoles irrespective of the composition of the perfusing solution.
当通过管腔向体内灌注非生理高浓度钠离子时,大鼠附睾上皮的外观发生了变化;在附睾尾部阈值浓度为30 mM - Na⁺、体部约为55 mM - Na⁺时,细胞间隙(ICS)扩张,这与管腔水的吸收有关。尽管ICS扩张,但连接复合体看起来完好无损,通过管腔辣根过氧化物酶(HRP)未进入ICS以及证明循环中的[³H]菊粉未进入管腔,证实了其完整性。附睾体主细胞中的滑面内质网和脂滴保存良好,附睾尾主细胞中粗面内质网的保存为该段蛋白质的持续分泌提供了形态学支持。然而,灌注3 - 6小时后,主细胞中偶尔可见高尔基体内池扩张或退化。与主细胞的多泡体不同,透明细胞特有的顶端和基底空泡大小会随不同灌注而改变。与主细胞的多泡体不同,透明细胞特有的顶端和基底空泡大小会随不同的灌注溶液而改变。当灌注低钠浓度溶液时,在附睾体和尾部透明细胞的顶端细胞质中经常发现大的半透明空泡,并且充满的空泡在附睾尾部变得更大且内容物密度降低。灌注高钠浓度溶液的组织中没有这些大空泡。通过灌注HRP证明了两种细胞类型的正常胞饮活性,HRP在主细胞中通过正常途径被摄取,并部分转移到高尔基体内池。无论灌注溶液的成分如何,到目前为止,最多的HRP积累在透明细胞的空泡中。