Androgen Receptor–Mediated Regulation of the α-Subunit of the Epithelial Sodium Channel in Human Kidney

التفاصيل البيبلوغرافية
العنوان: Androgen Receptor–Mediated Regulation of the α-Subunit of the Epithelial Sodium Channel in Human Kidney
المؤلفون: Paul M. Stewart, Marcus Quinkler, Sabine Buhner, Susan V. Hughes, Martin Hewison, Bruno Allolio, Kirren Kaur, Iwona J. Bujalska, Claire Onyimba
المصدر: Hypertension. 46:787-798
بيانات النشر: Ovid Technologies (Wolters Kluwer Health), 2005.
سنة النشر: 2005
مصطلحات موضوعية: Male, Epithelial sodium channel, medicine.medical_specialty, medicine.drug_class, Gene Expression, Biology, Kidney, Polymerase Chain Reaction, Sodium Channels, Flutamide, Kidney Tubules, Proximal, Mice, chemistry.chemical_compound, Genes, Reporter, Internal medicine, Internal Medicine, medicine, Animals, Humans, Testosterone, Kidney Tubules, Collecting, Epithelial Sodium Channels, Promoter Regions, Genetic, Cells, Cultured, Oligonucleotide Array Sequence Analysis, Androgen, Amiloride, Electrophysiology, Androgen receptor, Endocrinology, Blood pressure, medicine.anatomical_structure, chemistry, Receptors, Androgen, Steroids, Orchiectomy, medicine.drug
الوصف: Rodents studies suggest that androgens are involved in sex-specific differences in blood pressure. In humans, there is no difference in blood pressure between boys and girls, but after puberty, blood pressure increases more in men than in women. We investigated androgen-dependent regulation of the alpha-subunit of the epithelial sodium channel (alphaEnaC) in human kidney and in the human renal cell line immortalized human renal proximal tubular cell line (HKC-8). We used microarray technique to analyze androgen-dependent gene regulation and performed quantitative RT-PCR for verification. Promoter constructs for human alphaENaC were used in transfection studies to analyze the regulation by testosterone. We investigated the in vivo effect of testosterone on alphaENaC in a rat model and used the mouse collecting duct cell line M-1 for transepithelial electrophysiological measurements. The androgen receptor (AR) was expressed in male kidney and HKC-8 cells. AlphaENaC mRNA expression increased 2- to 3-fold after treatment with testosterone in HKC-8 cells. The induction by testosterone was completely blocked by adding the AR antagonist flutamide. Analysis of the alphaENaC promoter sequence identified a putative AR response element (ARE) located 140 nucleotides upstream from the transcription start site. HKC-8 cell transfection studies showed that testosterone directly upregulated gene expression via this ARE. In vivo, testosterone treatment of orchiectomized rats resulted in an increased renal alphaENaC mRNA expression. In testosterone-treated mouse M-1 cells, amiloride caused a significant stronger decrease in short circuit current than in control cells. These data show that alphaENaC expression is directly regulated by androgens in vitro and in vivo and highlight a potential mechanism explaining the reported gender differences in blood pressure.
تدمد: 1524-4563
0194-911X
DOI: 10.1161/01.hyp.0000184362.61744.c1
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f63b9c529b1a57e943c19192faf7504f
https://doi.org/10.1161/01.hyp.0000184362.61744.c1
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....f63b9c529b1a57e943c19192faf7504f
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15244563
0194911X
DOI:10.1161/01.hyp.0000184362.61744.c1