Solari Valeria, Piotrowska Anna Piaseczna, Cascio Salvatore, Unemoto Kei, Chertin Boris, Puri Prem
Children's Research Centre, Our Lady's Hospital for Sick Children and University College, Dublin, Ireland.
J Urol. 2003 Oct;170(4 Pt 2):1624-7. doi: 10.1097/01.ju.0000085810.37816.65.
Reflux nephropathy (RN) is a major cause of end stage renal failure in children and hypertension is a frequent complication. Cyclooxygenase-2 (COX-2) is an enzyme responsible for the prostaglandin synthesis. It has been shown that COX-2 up-regulates renin production leading to renovascular hypertension. We investigate COX-2 expression in the kidneys of children with RN.
Kidney specimens from 12 patients 2 to 13 years old with severe RN secondary to primary high grade vesicoureteral reflux obtained at the time of nephrectomy and 5 controls were examined. Single labeled immunohistochemistry was performed with 2 COX-2 antibodies using light and confocal microscopy. Quantification of COX-2 was determined by Western blotting analysis. COX-2 gene expression was evaluated by real-time quantitative reverse transcription polymerase chain reaction.
There was a strong COX-2 immunoreactivity in the proximal tubules and tubulointerstitial space in the RN samples compared to controls. Immunoreactive COX-2 protein expression was markedly increased in RN samples compared to controls. Real-time reverse transcription polymerase chain reaction showed a significant increase in COX-2 mRNA expression in the RN samples compared to controls (p <0.05).
Over expression of COX-2 in reflux nephropathy suggests that COX-2 may be involved in the pathogenesis of tubulointerstitial damage associated with severe reflux nephropathy.
反流性肾病(RN)是儿童终末期肾衰竭的主要原因,高血压是常见并发症。环氧化酶-2(COX-2)是一种负责前列腺素合成的酶。研究表明,COX-2上调肾素生成,导致肾血管性高血压。我们研究了RN患儿肾脏中COX-2的表达情况。
检查了12例2至13岁因原发性重度膀胱输尿管反流继发严重RN的患者在肾切除时获取的肾脏标本以及5例对照。使用2种COX-2抗体通过光镜和共聚焦显微镜进行单标记免疫组化。通过蛋白质印迹分析对COX-2进行定量。通过实时定量逆转录聚合酶链反应评估COX-2基因表达。
与对照组相比,RN样本中近端小管和肾小管间质空间存在强烈的COX-2免疫反应性。与对照组相比,RN样本中免疫反应性COX-2蛋白表达明显增加。实时逆转录聚合酶链反应显示,与对照组相比,RN样本中COX-2 mRNA表达显著增加(p<0.05)。
反流性肾病中COX-2的过度表达表明,COX-2可能参与了与严重反流性肾病相关的肾小管间质损伤的发病机制。