Cyr D G, Hermo L, Blaschuk O W, Robaire B
Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec, Canada.
Endocrinology. 1992 Jan;130(1):353-63. doi: 10.1210/endo.130.1.1727709.
The epithelium of the epididymis possesses an elaborate network of tight junctions between principal cells which is altered as a function of postnatal age. Cadherins are implicated in the formation of tight junctions. The objective of the present study was to determine whether RNA transcripts for cadherins were present in the epididymis, and if so, how they were hormonally regulated. Using specific cDNA probes for epithelial cadherin (E-Cad) and neural cadherin (N-Cad), Northern blot analysis was used to study steady state levels of cadherin mRNAs. A major E-Cad mRNA species of 4.7 kilobases and a weaker 4.3-kilobase species were observed in the epididymis. No signal for N-Cad was detected. Steady state mRNA levels for E-Cad were highest in the caput and corpus epididymidis and were almost 4 times higher than those in the initial segments and cauda epididymidis; no signal was detected in the vas deferens. Light microscopic immunocytochemical localization of E-Cad revealed a reaction over the principal cells of the entire epididymis. The relative intensities of the immunoreactivity suggested that the E-Cad protein concentration was highest in the corpus, followed by the caput, cauda, and initial segments of the epididymis. There was no reaction over the epithelial basal and clear cells or intraepithelial halo cells. Three days after bilateral orchidectomy, E-cad mRNA was decreased by 75% in the caput epididymidis. A dose-dependent maintenance of mRNA concentration for E-Cad was observed throughout the epididymis of orchidectomized rats after replacement with testosterone. Fourteen days after unilateral orchidectomy, no differences were observed in the concentrations of epididymal E-Cad mRNA between control and unilaterally orchidectomized rats. Together, these data demonstrate that mRNA for E-Cad is present and translated in the rat epididymis, is differentially distributed along this tissue, and can be regulated by circulating androgens.
附睾上皮在主细胞之间拥有一个复杂的紧密连接网络,该网络会随着出生后的年龄而发生变化。钙黏蛋白与紧密连接的形成有关。本研究的目的是确定附睾中是否存在钙黏蛋白的RNA转录本,如果存在,它们是如何受到激素调节的。使用上皮钙黏蛋白(E-Cad)和神经钙黏蛋白(N-Cad)的特异性cDNA探针,通过Northern印迹分析来研究钙黏蛋白mRNA的稳态水平。在附睾中观察到一种主要的4.7千碱基的E-Cad mRNA种类和一种较弱的4.3千碱基的种类。未检测到N-Cad的信号。E-Cad的稳态mRNA水平在附睾头和附睾体中最高,几乎是起始段和附睾尾中水平的4倍;在输精管中未检测到信号。E-Cad的光镜免疫细胞化学定位显示在整个附睾的主细胞上有反应。免疫反应的相对强度表明,E-Cad蛋白浓度在附睾体中最高,其次是附睾头、附睾尾和起始段。上皮基底细胞、透明细胞或上皮内晕细胞上没有反应。双侧睾丸切除术后3天,附睾头中的E-cad mRNA减少了75%。在用睾酮替代后,在去势大鼠的整个附睾中观察到E-Cad mRNA浓度呈剂量依赖性维持。单侧睾丸切除术后14天,对照大鼠和单侧去势大鼠附睾E-Cad mRNA的浓度没有差异。总之,这些数据表明,E-Cad的mRNA在大鼠附睾中存在并被翻译,在该组织中呈差异分布,并且可以受到循环雄激素的调节。