Department of Cytology and Histology, Faculty of Veterinary Medicine, Minufiya University, Sadat City Branch, Egypt.
Acta Histochem. 2012 Nov;114(7):682-94. doi: 10.1016/j.acthis.2011.12.003. Epub 2011 Dec 26.
Prenatal development of the epididymis was studied in bovine fetuses ranging from 10 to 90cm crown-rump length (CRL) (75-285 pcd). The studies aimed to apply both glycohistochemistry and immunohistochemistry for the detection of the differentiation of the developing prenatal epididymis. Both conventional histological and histochemical techniques were applied on paraffin sections of the epididymis from different fetal stages. Establishment of the urogenital junction between the extra-testicular rete testis and the mesonephric duct, via the growing efferent ductules (ductuli efferentes) was first evident in fetuses with 10cm CRL. At the fetal age of 110 pcd (24cm CRL), the mesonephric duct began to lengthen and coil forming three distinct regions (caput, corpus and cauda). In addition to the macroscopical modifications in the extra-testicular excurrent duct system, histological differentiation involved both the tubular epithelial and the peritubular mesenchymal cells. The epithelium lining the efferent ductules was differentiated into ciliated and non-ciliated columnar cells. The simple epithelium of the epididymal duct increased in height and developed stereocilia on the apical surface. Additionally, some basal cells first appeared at 185 pcd (56cm CRL), within the epithelium lining the cauda only. Lectin histochemistry (WGA, PNA, GSA-I) showed early immunostaining in epithelium of the efferent ductules and in peritubular mesenchymal structures. Immunoreactivity for different proteins (S-100, fibroblast growth factor-1 and factor-2, angiotensin converting enzyme, laminin, alpha-smooth muscle actin) was evident, both in the epithelial and in the peritubular mesenchymal cells as early as at 75 pcd. On the basis of our histochemical observations, we conclude that both glycohistochemistry and immunohistochemistry are useful tools to demonstrate that the differentiation in the peritubular structures and efferent ductular epithelium begins earlier than other components.
本研究旨在通过糖基组织化学和免疫组织化学检测方法,对牛胎儿 10 至 90cm 头臀长(crown-rump length,CRL)(75-285 胚龄)阶段的附睾进行研究,以探讨其产前发育过程。本研究采用石蜡切片对不同胎龄阶段的附睾进行常规组织学和组织化学技术处理。在 10cm CRL 的胎儿中,首先可以观察到睾丸网外输出小管(efferent ductules)和中肾管之间的尿生殖窦建立。在 110pcd(24cm CRL)时,中肾管开始延长并盘绕形成三个不同的区域(头、体和尾)。除了外输出导管系统的宏观变化外,组织学分化还涉及管状上皮和小管周围的间充质细胞。输出小管的内衬上皮分化为纤毛和非纤毛柱状细胞。附睾管的简单上皮细胞高度增加,并在顶表面发育出微绒毛。此外,在 185pcd(56cm CRL)时,仅在尾部的上皮中首次出现一些基底细胞。凝集素组织化学(WGA、PNA、GSA-I)显示,在输出小管的上皮和小管周围的间充质结构中,早期就有免疫染色。在 75pcd 时,就已经可以在上皮和小管周围的间充质细胞中观察到不同蛋白(S-100、成纤维细胞生长因子 1 和 2、血管紧张素转换酶、层粘连蛋白、α-平滑肌肌动蛋白)的免疫反应性。基于我们的组织化学观察结果,我们得出结论,糖基组织化学和免疫组织化学都是有用的工具,可以证明小管周围结构和输出小管上皮的分化比其他成分更早开始。