Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Steroids. 2013 Feb;78(2):220-7. doi: 10.1016/j.steroids.2012.10.004. Epub 2012 Nov 2.
Testosterone (T) is known to induce persistent susceptibility to blood-stage malaria of Plasmodium chabaudi in otherwise resistant female C57BL/6 mice, which is associated with permanent changes in mRNA expression of the liver. Here, we investigate the spleen as the major effector against blood-stage malaria for any possible T-induced long-term effects on lincRNA and mRNA expression. Female C57BL/6 mice were treated with T for 3 weeks, then T was withdrawn for 12 weeks before challenging with P. chabaudi. LincRNA and mRNA expression was examined after 12 weeks of T-withdrawal and after subsequent infections using Agilent whole mouse genome oligo microarrays. Our data show for the first time long-term effects of T on lincRNA expression evidenced directly as persistent changes after T-withdrawal for 12 weeks and indirectly as altered responsiveness of expression to P. chabaudi infections. There are 3 lincRNA-species upregulated and 10 lincRNAs downregulated by more than 2-fold (p<0.01). In addition, 11 and 10 mRNAs are persistently up- and downregulated by T, respectively. These changes remain not sustained during infections at peak parasitemia, when 15 other lincRNAs and 9 other mRNAs exhibit an altered expression. The only exception is the Tnk1-mRNA encoding the non-receptor tyrosine kinase 1 that is persistently downregulated by 0.34-fold after T-withdrawal and that becomes upregulated by 5.9-fold upon infection at peak parasitemia, suggesting an involvement of tyrosine phosphorylation by Tnk1 in mediating long-term effects of T in the spleen. The T-induced changes in splenic mRNA expression are totally different to those previously observed in the liver. Collectively, our data support the view that T induces long-term organ-specific changes in both lincRNA and mRNA expression, that presumably contribute to organ-specific dysfunctions upon infection with blood-stage malaria of P. chabaudi.
睾酮(T)已知可诱导原本具有抗性的 C57BL/6 雌性小鼠对疟原虫 chabaudi 的血期疟疾持续易感,这与肝脏中 mRNA 表达的永久性变化有关。在这里,我们研究了脾脏作为对抗血期疟疾的主要效应器,以研究 T 是否对 lincRNA 和 mRNA 表达产生任何可能的长期影响。雌性 C57BL/6 小鼠用 T 治疗 3 周,然后在用 P. chabaudi 攻毒前停用 T 12 周。在停用 T 12 周后和随后的感染后,使用安捷伦全鼠基因组 oligo 微阵列检查 lincRNA 和 mRNA 的表达。我们的数据首次显示 T 对 lincRNA 表达的长期影响,直接表现为停用 T 12 周后持续变化,间接表现为对 P. chabaudi 感染的表达反应性改变。有 3 种 lincRNA 物种上调,10 种 lincRNA 下调超过 2 倍(p<0.01)。此外,有 11 个和 10 个 mRNA 分别被 T 持续上调和下调。这些变化在峰值寄生虫血症期间的感染中并未持续,此时 15 个其他 lincRNA 和 9 个其他 mRNA 的表达发生改变。唯一的例外是 Tnk1-mRNA,它编码非受体酪氨酸激酶 1,在停用 T 后持续下调 0.34 倍,在峰值寄生虫血症时感染时上调 5.9 倍,这表明 Tnk1 的酪氨酸磷酸化参与介导 T 在脾脏中的长期作用。T 诱导的脾脏 mRNA 表达变化与之前在肝脏中观察到的变化完全不同。总的来说,我们的数据支持这样一种观点,即 T 诱导 lincRNA 和 mRNA 表达的长期器官特异性变化,这可能有助于感染疟原虫 chabaudi 的血期疟疾时器官特异性功能障碍。