Ezer Nadine, Robaire Bernard
Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec H3G 1Y6, Canada.
Endocrinology. 2003 Mar;144(3):975-88. doi: 10.1210/en.2002-220705.
The epididymis is the site for the transport, maturation, and storage of spermatozoa. Regulation of epididymal structure and function is highly dependent on the ipsilateral testis. At the molecular level, however, few studies have been undertaken to determine which genes are expressed in the epididymis under testicular regulation. The goal of this study was to identify genes for which expression is regulated after orchidectomy, both throughout the epididymis and in a segment-specific manner. Microarrays spotted with 474 rat cDNAs were used to examine gene expression changes over the first 7 d post orchidectomy in the initial segment, caput, corpus, and cauda epididymidis of the adult Brown Norway rat. Using k-means cluster analysis, we show that four patterns of gene expression are activated in each epididymal segment over the first week following orchidectomy. Transient up-regulation of gene expression in the epididymis after orchidectomy is described for the first time. Potential androgen-repressed genes, including Gpx-1, show increased expression in the epididymis after orchidectomy. Several glutathione-S-transferases and calcium-binding proteins decline throughout the epididymis after orchidectomy, indicating that these may be novel androgen-regulated epididymal genes. Other genes coding for metabolism-associated proteins, transporters, and alpha-1 acid glycoprotein show segment-specific regulation in the epididymis after orchidectomy. Finally, we describe the expression of the previously uncharacterized heat shock proteins, and apoptosis-associated genes in the epididymis after orchidectomy. Thus, gene expression in the epididymis is differentially affected over time after orchidectomy. These results provide novel insight into androgen-dependent and segment-specific epididymal function.
附睾是精子运输、成熟和储存的场所。附睾结构和功能的调节高度依赖同侧睾丸。然而,在分子水平上,很少有研究确定在睾丸调节下附睾中表达哪些基因。本研究的目的是鉴定在睾丸切除术后整个附睾以及以节段特异性方式表达受到调节的基因。用点有474个大鼠cDNA的微阵列检测成年棕色挪威大鼠睾丸切除术后第1至7天附睾起始段、头段、体段和尾段的基因表达变化。使用k均值聚类分析,我们发现在睾丸切除术后的第一周,每个附睾节段有四种基因表达模式被激活。首次描述了睾丸切除术后附睾中基因表达的短暂上调。包括Gpx-1在内的潜在雄激素抑制基因在睾丸切除术后附睾中的表达增加。睾丸切除术后,几种谷胱甘肽-S-转移酶和钙结合蛋白在整个附睾中表达下降,表明这些可能是新的雄激素调节的附睾基因。其他编码代谢相关蛋白、转运蛋白和α-1酸性糖蛋白的基因在睾丸切除术后在附睾中表现出节段特异性调节。最后,我们描述了睾丸切除术后附睾中以前未鉴定的热休克蛋白和凋亡相关基因的表达。因此,睾丸切除术后附睾中的基因表达随时间受到不同影响。这些结果为雄激素依赖和节段特异性附睾功能提供了新的见解。