Veri J P, Hermo L, Robaire B
Department of Anatomy and Cell Biology, McGill University, Montréal, Québec, Canada.
J Androl. 1994 Sep-Oct;15(5):415-34.
The glutathione S-transferases (GSTs) are a family of isozymes that catalyze the conjugation of glutathione with electrophiles. These proteins exist as homo- or heterodimers and are separated into five classes (alpha, mu, pi, theta, and sigma). In the present study, the distribution of the GST Yo subunit, a member of the mu family, was examined immunocytochemically in the adult rat testis and epididymis using both light microscopy (LM) and electron microscopy (EM). In the testis, an intense immunoperoxidase reaction was observed over Leydig cells but not macrophages. Within the seminiferous epithelium, only weak reactivity was noted over Sertoli cells, spermatogonia, spermatocytes, and step 1-15 spermatids. There was, however, a progressive and dramatic increase in the intensity of staining in the cytoplasmic lobes of spermatids between steps 16 and 19. Residual bodies, representing the detached cytoplasmic lobes of the late step 19 spermatids, were also intensely stained. Initially seen near the lumen of the tubule, they eventually appeared at different levels of the tubule at stages IX-XI; none were present at stage XII. Cytoplasmic droplets of step 19 spermatids were also intensely reactive. After spermiation, the cytoplasmic droplets of spermatozoa within the proximal region of the epididymis remained intensely stained. A noticeable decrease in staining was observed in the cauda epididymidis in those droplets that were still there. Quantitation of the labeling density (number of gold particles representing anti-Yo antigenic sites/microns 2) paralleled the LM results; for example, between step 15 and 19 spermatids, a greater than sevenfold increase in labeling density was noted. In the epididymis, a progressive increase in immunoreactivity was observed over epithelial principal cells from the initial segment to the cauda region of this tissue. There was little reactivity over basal, halo, or clear cells. In all reactive cells, gold particles were distributed randomly throughout the cytoplasmic matrix and nucleus. The present work thus demonstrates that, at the end of spermiogenesis, the GST Yo subunit is expressed at high levels in late spermatids. Furthermore, the presence of this protein in late spermatids and cytoplasmic droplets of spermatozoa suggests that this conjugating enzyme may play a role in protecting these cells from electrophilic attack. Also interesting is the correlation between the loss of reactivity in cytoplasmic droplets of spermatozoa of the distal region of the epididymis and the concomitant increase of reactivity in principal cells of this region.
谷胱甘肽S-转移酶(GSTs)是一类同工酶,可催化谷胱甘肽与亲电试剂的结合。这些蛋白质以同二聚体或异二聚体形式存在,分为五类(α、μ、π、θ和σ)。在本研究中,使用光学显微镜(LM)和电子显微镜(EM),通过免疫细胞化学方法检测了成年大鼠睾丸和附睾中μ家族成员GST Yo亚基的分布。在睾丸中,在睾丸间质细胞上观察到强烈的免疫过氧化物酶反应,但巨噬细胞上没有。在生精上皮内,仅在支持细胞、精原细胞、精母细胞和1-15期精子细胞上观察到弱阳性反应。然而,在16-19期精子细胞的细胞质小叶中,染色强度逐渐显著增加。残余小体,代表19期末期精子细胞分离的细胞质小叶,也被强烈染色。最初在小管腔附近可见,它们最终在IX-XI期出现在小管的不同水平;在XII期不存在。19期精子细胞的细胞质滴也有强烈反应。精子排出后,附睾近端区域精子的细胞质滴仍被强烈染色。在附睾尾部仍存在的那些滴中,染色明显减少。标记密度(代表抗Yo抗原位点的金颗粒数/μm²)的定量与光学显微镜结果平行;例如,在15-19期精子细胞之间,标记密度增加了七倍以上。在附睾中,从该组织的起始段到尾部区域,上皮主细胞的免疫反应性逐渐增加。在基底细胞、晕细胞或透明细胞上几乎没有反应性。在所有反应性细胞中,金颗粒随机分布在整个细胞质基质和细胞核中。因此,本研究表明,在精子发生末期,GST Yo亚基在晚期精子细胞中高水平表达。此外,这种蛋白质在晚期精子细胞和精子细胞质滴中的存在表明,这种结合酶可能在保护这些细胞免受亲电攻击方面发挥作用。同样有趣的是,附睾远端区域精子细胞质滴中反应性的丧失与该区域主细胞中反应性的相应增加之间的相关性。