Adamali H I, Hermo L
Department of Anatomy and Cell Biology, McGill University, Montreal, Canada.
J Androl. 1996 May-Jun;17(3):208-22.
Apical and narrow cells of the initial segment and intermediate zone of the adult rat epididymis were glutaraldehyde fixed and Epon embedded for routine light (LM) and electron (EM) microscopic analysis and Bouin fixed and paraffin embedded for LM immunocytochemical analysis in order to examine their structural features, distribution, and functions. The goblet-shaped apical cells comprised 10.7 +/- 1.0% of the total epithelial population in the proximal initial segment but only 1.3 +/- 0.5% in the intermediate zone. In the EM, these cells presented numerous mitochondria, few C-shaped vesicles, and a pale round or oblong nucleus located in the upper half of their cytoplasm. The slender elongated narrow cells increased from 2.8 +/- 0.3% in the proximal initial segment to 6.3 +/- 0.4% in the intermediate zone. In an EM analysis, these cells presented numerous C-shaped vesicles and mitochondria and a small flattened nucleus located in the upper half of their cytoplasm. The structural features of both these cell types differed not only from each other but also from the neighboring principal and basal cells of each region. Of the various antibodies examined to lysosomal proteins, narrow and apical cells expressed high levels of cathepsin D, while beta-hexosaminidase A was expressed at high levels in narrow cells but only moderately in apical cells. Apical cells were intensely reactive for the Yf subunit of glutathione S-transferase (GST)-P, whereas no reaction was seen in narrow cells; the Yo subunit of GST was localized within both cell types but only in the proximal initial segment. Narrow cells exclusively expressed carbonic anhydrase II. Selective differences in the immunolocalization of these various proteins were also noted between these two cell types and principal and basal cells. The localization of cathepsin D and beta-hexosaminidase A within narrow and apical cells suggests these cells may be involved in the degradation of specific proteins within their lysosomes, whereas the presence of GSTs may aid in protecting spermatozoa from a changing environment of harmful electrophiles. Localization of carbonic anhydrase II exclusively within narrow cells suggests that these cells may modify the pH of the lumen resulting in the quiescence of sperm motility in the proximal end of the epididymis. Together, the data indicate that apical and narrow cells differ not only from each other but also from principal and basal cells in their structure and relative distribution. They also express different proteins within the distinct epididymal regions, indicating that they perform different functions.
成年大鼠附睾起始段和中间区的顶端细胞和狭窄细胞用戊二醛固定,环氧树脂包埋,用于常规光镜(LM)和电镜(EM)分析;用Bouin固定液固定,石蜡包埋,用于LM免疫细胞化学分析,以研究它们的结构特征、分布和功能。杯状顶端细胞在近端起始段占上皮细胞总数的10.7±1.0%,而在中间区仅占1.3±0.5%。在电镜下,这些细胞有大量线粒体、少量C形小泡,细胞核呈淡圆形或椭圆形,位于细胞质上半部分。细长的狭窄细胞在近端起始段占2.8±0.3%,在中间区增加到6.3±0.4%。电镜分析显示,这些细胞有大量C形小泡和线粒体,细胞核小而扁平,位于细胞质上半部分。这两种细胞类型的结构特征不仅彼此不同,也与每个区域相邻的主细胞和基底细胞不同。在所检测的各种溶酶体蛋白抗体中,狭窄细胞和顶端细胞表达高水平的组织蛋白酶D,而β - 氨基己糖苷酶A在狭窄细胞中高水平表达,在顶端细胞中仅中度表达。顶端细胞对谷胱甘肽S - 转移酶(GST)-P的Yf亚基呈强反应性,而狭窄细胞无反应;GST的Yo亚基在两种细胞类型中均有定位,但仅在近端起始段。狭窄细胞仅表达碳酸酐酶II。在这两种细胞类型与主细胞和基底细胞之间,还发现了这些不同蛋白质免疫定位的选择性差异。组织蛋白酶D和β - 氨基己糖苷酶A在狭窄细胞和顶端细胞中的定位表明,这些细胞可能参与其溶酶体内特定蛋白质的降解,而GST的存在可能有助于保护精子免受有害亲电试剂变化环境的影响。碳酸酐酶II仅在狭窄细胞中定位,表明这些细胞可能调节管腔pH值,导致附睾近端精子运动静止。总之,数据表明顶端细胞和狭窄细胞不仅彼此不同,而且在结构和相对分布上也与主细胞和基底细胞不同。它们在不同的附睾区域还表达不同的蛋白质,表明它们执行不同的功能。