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首页> 外文期刊>BMC Molecular Biology >Expression of HNF4alpha in the human and rat choroid plexus - Implications for drug transport across the blood-cerebrospinal-fluid (CSF) barrier
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Expression of HNF4alpha in the human and rat choroid plexus - Implications for drug transport across the blood-cerebrospinal-fluid (CSF) barrier

机译:HNF4alpha在人和大鼠脉络丛中的表达-跨血脑脊液(CSF)屏障的药物转运的含义

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Background The choroid plexus consists of highly differentiated epithelium and functions as a barrier at the interface of the blood-cerebrospinal-fluid (CSF). This tissue may therefore determine the bioavailability and transport of drugs to the brain. Little is known about the expression of drug and xenobiotic metabolizing enzymes (DME) and of drug transporters in the human choroid plexus. Notably, the transcription factor and zinc finger protein HNF4alpha is a master regulator of DMEs and of drug transporters. As of today its activity in the blood-CSF barrier is unknown. Here we report our efforts in determining HNF4alpha activity in the regulation of ABC transporters in the human and rat choroid plexus.Results We report expression of HNF4alpha by qRT-PCR and by immunohistochemistry and evidence transcript expression of the ATP-binding cassette transporters ABCB1, ABCB4, ABCC1-6 in choroid plexus. Additionally, HNF4alpha DNA binding activity at regulatory sequences of ABCB4 and ABCC1 was determined by EMSA bandshift assays with a specific antibody. We then performed siRNA mediated functional knock down of HNF4alpha in Caco-2 cells and found ABCC1 gene expression to be repressed in cell culture experiments.Conclusion Our study evidences activity of HNF4alpha in human and rat choroid plexus. This transcription factor targets DMEs and drug transporters and may well determine availability of drugs at the blood-CSF barrier.
机译:背景脉络丛由高度分化的上皮组成,在血脑脊髓液(CSF)的界面处起屏障作用。因此,该组织可以确定药物的生物利用度和向大脑的运输。关于人脉络丛中药物和异种代谢酶(DME)以及药物转运蛋白的表达知之甚少。值得注意的是,转录因子和锌指蛋白HNF4alpha是DME和药物转运蛋白的主要调节剂。到目前为止,它在血液-CSF屏障中的活性尚不清楚。我们在这里报告了我们在确定人和大鼠脉络丛ABC转运蛋白中HNF4alpha活性方面所做的努力。结果我们通过qRT-PCR和免疫组化报告了HNF4alpha的表达,并证明了ATP结合盒转运蛋白ABCB1,ABCB4的转录本表达,在脉络丛中为ABCC1-6。另外,通过具有特定抗体的EMSA频移测定法确定了在ABCB4和ABCC1调控序列上的HNF4alpha DNA结合活性。然后,我们在Caco-2细胞中进行了siRNA介导的HNF4alpha的功能性敲低,发现ABCC1基因表达在细胞培养实验中受到抑制。结论我们的研究证明了HNF4alpha在人和大鼠脉络丛中的活性。该转录因子靶向DME和药物转运蛋白,并可以很好地确定血液CSF屏障处药物的可用性。

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