Sipilä Petra, Krutskikh Anton, Pujianto Dwi Ari, Poutanen Matti, Huhtaniemi Ilpo
Department of Physiology, Institute of Biomedicine, University of Turku, Turku, Finland.
J Androl. 2011 Nov-Dec;32(6):711-7. doi: 10.2164/jandrol.110.012914. Epub 2011 Jul 15.
Endocrine regulation of the mouse initial segment (IS) and distal caput epididymides was studied using genome-wide profiling of gene expression. Among the IS-enriched genes, 29% were significantly down-regulated 1 day after gonadectomy. Of those genes, dihydrotestosterone (DHT) supplementation was not sufficient to maintain their pregonadectomy level of expression in 70%. Of the caput-enriched genes, 16% were significantly down-regulated after gonadectomy, and of those genes, DHT supplementation did not maintain the initial level of expression in 28%. Identical data were obtained by clustering analyses performed for the expression data of epididymal genes. Furthermore, the microarray data revealed that 26 androgen receptor coregulators were expressed in the epididymis, of which several were confirmed by quantitative reverse transcriptase polymerase chain reaction analysis. This suggests putative involvement of these proteins in the segment-specific regulation of the epididymal genes. The pattern of epididymal gene expression in the novel proximal epididymis-specific androgen receptor knockout mouse ProxE-ARKO, with severe hypotrophy and hypoplasia of the caput epithelium, furthermore suggested that a subset of genes whose expression cannot be maintained by systemic androgen alone still require either direct lumicrine androgen action or a permissive effect of circulating testosterone. It is evident that testicular factors, one of which could be the high-concentration luminal androgen, are important for the expression of IS-enriched genes, whereas the expression of distal caput-enriched genes is typically regulated by systemic androgens.
利用全基因组基因表达谱分析,研究了小鼠附睾起始段(IS)和远侧头部的内分泌调节。在IS富集的基因中,29%在去势后1天显著下调。在这些基因中,70%的基因补充双氢睾酮(DHT)不足以维持其去势前的表达水平。在头部富集的基因中,16%在去势后显著下调,在这些基因中,28%的基因补充DHT后不能维持初始表达水平。对附睾基因表达数据进行聚类分析,得到了相同的数据。此外,微阵列数据显示,26种雄激素受体共调节因子在附睾中表达,其中几种通过定量逆转录聚合酶链反应分析得到证实。这表明这些蛋白质可能参与附睾基因的节段特异性调节。新型近端附睾特异性雄激素受体敲除小鼠ProxE-ARKO中附睾基因的表达模式,其头部上皮严重萎缩和发育不全,进一步表明,仅靠全身性雄激素无法维持其表达的一部分基因,仍需要直接的管腔雄激素作用或循环睾酮的允许作用。很明显,睾丸因子(其中之一可能是高浓度的管腔雄激素)对IS富集基因的表达很重要,而远侧头部富集基因的表达通常受全身性雄激素调节。