Flores Katiria, Manautou José E, Renfro J Larry
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT, USA.
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT, USA.
Toxicology. 2017 Jul 1;386:84-92. doi: 10.1016/j.tox.2017.05.019. Epub 2017 Jun 3.
The choroid plexus (CP) and blood-brain barrier (BBB) control the movement of several drugs and endogenous compounds between the brain and systemic circulation. The multidrug resistance associated protein (Mrp) efflux transporters form part of these barriers. Several Mrp transporters are positively regulated by the transcription factor nuclear factor erythroid-2-related factor (Nrf2) in liver. The Mrps, Nrf2 and Nrf2-dependent genes are cytoprotective and our aim was to examine basal gender differences in expression of Mrp transporters, Nrf2 and Nrf2-dependent genes (Nqo1 and Ho-1) in the brain-barriers. Previous studies have shown higher expression of Mrp1, Mrp2 and Mrp4 in female mouse liver and kidney. We hypothesized that similar renal/hepatic gender-specific patterns are present in the brain-barrier epithelia interfaces. qPCR and immunoblot analyses showed that Mrp4, Ho-1 and Nqo1 expression was higher in female CP. Mrp1, Mrp2 and Nrf2 expression in the CP had no gender pattern. Female Mrp1, Mrp2 and Mrp4 mouse brain expressions in remaining brain areas, excluding CP, were higher than male. Functional analysis of Mrp4 in CP revealed active accumulation of the Mrp4 model substrate fluo-cAMP. WT female CP had 10-fold higher accumulation in the vascular spaces than males and 60% higher than Mrp4 females. Probenecid blocked all transport. Methotrexate did as well except in Mrp4 females where it had no effect, suggesting compensatory induction of transport occurred in Mrp4. Collectively, our findings indicate significant gender differences in expression of Mrp transporters and cytoprotective genes in the CP and BBB.
脉络丛(CP)和血脑屏障(BBB)控制着多种药物和内源性化合物在脑与体循环之间的移动。多药耐药相关蛋白(Mrp)外排转运体是这些屏障的一部分。在肝脏中,几种Mrp转运体受转录因子核因子红细胞2相关因子(Nrf2)的正向调控。Mrp、Nrf2和Nrf2依赖基因具有细胞保护作用,我们的目的是研究脑屏障中Mrp转运体、Nrf2和Nrf2依赖基因(Nqo1和Ho-1)表达的基础性别差异。先前的研究表明,Mrp1、Mrp2和Mrp4在雌性小鼠肝脏和肾脏中的表达较高。我们假设在脑屏障上皮界面存在类似的肾/肝性别特异性模式。定量聚合酶链反应(qPCR)和免疫印迹分析表明,Mrp4、Ho-1和Nqo1在雌性脉络丛中的表达较高。脉络丛中Mrp1、Mrp2和Nrf2的表达没有性别模式。在除脉络丛外的其余脑区,雌性小鼠Mrp1、Mrp2和Mrp4的脑表达高于雄性。脉络丛中Mrp4的功能分析显示,Mrp4模型底物荧光环磷酸腺苷(fluo-cAMP)有活跃积累。野生型雌性脉络丛在血管间隙中的积累比雄性高10倍,比Mrp4基因敲除雌性高60%。丙磺舒阻断了所有转运。甲氨蝶呤也有同样的效果,但在Mrp4基因敲除雌性中无效,这表明在Mrp4基因敲除雌性中发生了转运的代偿性诱导。总的来说,我们的研究结果表明,脉络丛和血脑屏障中Mrp转运体和细胞保护基因的表达存在显著的性别差异。