Shannonhouse John L, Urbanski Henryk F, Woo Shih-Lung, Fong Li An, Goddard Scott D, Lucas William F, Jones Edward R, Wu Chaodong, Morgan Caurnel
Institute for Neuroscience, Texas A&M University, College Station, TX 77843, USA.
Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR 97006, USA.
Mol Cell Endocrinol. 2014 Jun 25;391(1-2):1-9. doi: 10.1016/j.mce.2014.04.011. Epub 2014 Apr 30.
The present study sought novel changes to the hamster testicular transcriptome during modulation of fertility by well-characterized photoperiodic stimuli. Transition from long days (LD, 14 h light/day) to short days (SD, 10h light/day) triggered testicular regression (61% reduction of testis weight, relative to LD) in SD-sensitive (SD-S) hamsters within 16 weeks. After 22 weeks of SD exposure, a third cohort of hamsters became SD-refractory (SD-R), and exhibited testicular recrudescence (137% testis weight gain, relative to SD-S). Partial interrogation of the testicular transcriptome by annealing-control-primer-modified differential display PCR provided several candidates for regulation of testicular functions. Multiple linear regression modeling indicated the best correlation for aquaporin 11 (Aqp11) with changes in testis weight. Correlations were also strongest for Aqp11 with expression levels of reference cDNAs that control spermatogenesis (Hspa2 and Tnp2), steroidogenesis (Cox2, 3βHsd, and Srebp2), sperm motility (Catsper1, Pgk2, and Tnp2), inflammation (Cox2), and apoptosis (Bax and Bcl2). Moreover, siRNA-mediated knockdown of testicular Aqp11 mRNA and protein reduced Hspa2 and Tnp2 mRNA levels, and it increased 3βHsd mRNA levels. It also reduced mRNA levels for Sept12, which is a testis-specific inducer of spermatogenesis. These results suggest a central role for testicular Aqp11 signaling in the coordinate regulation of crucial components of fertility.
本研究旨在探寻在特征明确的光周期刺激调节生育力过程中,仓鼠睾丸转录组的新变化。对光周期敏感(SD-S)的仓鼠,从长日照(LD,14小时光照/天)过渡到短日照(SD,10小时光照/天),在16周内引发了睾丸退化(相对于LD,睾丸重量减少61%)。暴露于SD 22周后,第三组仓鼠变得对SD不敏感(SD-R),并表现出睾丸再发育(相对于SD-S,睾丸重量增加137%)。通过退火控制引物修饰的差异显示PCR对睾丸转录组进行部分分析,提供了几个可能参与调节睾丸功能的候选基因。多元线性回归模型表明水通道蛋白11(Aqp11)与睾丸重量变化的相关性最佳。Aqp11与控制精子发生(Hspa2和Tnp2)、类固醇生成(Cox2、3βHsd和Srebp2)、精子活力(Catsper1、Pgk2和Tnp2)、炎症(Cox2)和细胞凋亡(Bax和Bcl2)的参考cDNA表达水平的相关性也最强。此外,siRNA介导的睾丸Aqp11 mRNA和蛋白敲低降低了Hspa2和Tnp2 mRNA水平,并增加了3βHsd mRNA水平。它还降低了Sept12的mRNA水平,Sept12是睾丸特异性的精子发生诱导因子。这些结果表明睾丸Aqp11信号在生育力关键成分的协调调节中起核心作用。