Ceol Monica, Gianesello Lisa, Tosetto Enrica, Priante Giovanna, Del Prete Dorella, Anglani Franca
Kidney Histomorphology and Molecular Biology Laboratory, Clinical Nephrology Unit, Department of Medicine-DIMED, University of Padua, Padua, Italy
Kidney Histomorphology and Molecular Biology Laboratory, Clinical Nephrology Unit, Department of Medicine-DIMED, University of Padua, Padua, Italy.
J Investig Med. 2020 Apr;68(4):864-869. doi: 10.1136/jim-2019-001205. Epub 2020 Feb 3.
ClC-5, the electrogenic chloride/proton exchanger strongly expressed in renal proximal tubules, belongs to the endocytic macromolecular complex responsible for albumin and low-molecular-weight protein uptake. ClC-5 was found to be overexpressed in glomeruli of glomerulonephritis and in cultured human podocytes under albumin overload. The transcriptional regulation of human ClC-5 is not fully understood. Three functional promoters of various strengths and 11 different 5' untranslated region (5'UTR) isoforms of messenger RNA (mRNA) were detected in the human kidney (variants 1-11). The aim of this study was to investigate the expression pattern of 5 5'UTR variants and the common translated region in glomerulonephritis. The 5'UTR ends and the translated region of mRNA were analyzed using quantitative relative real-time PCR or quantitative comparative endpoint PCR with as housekeeping gene in 8 normal kidneys and 12 renal biopsies from patients with glomerulonephritis. The expression profile for all variants in normal and glomerulonephritis biopsies was similar, and variant 3 and alternative variant 4 were the most abundantly expressed in both sets. In glomerulonephritis biopsies, isoforms under the control of a weak promoter (variants 4, 6 and 7) showed an increased expression leading to an increase in the translated region, underscoring their importance in kidney pathophysiology. Since weak promoters can be turned on by different stimuli, these data support the hypothesis that proteinuria could be one of the stimuli capable of starting a signaling pathway that induces an increase in transcription.
ClC-5是一种在肾近端小管中强烈表达的电生性氯化物/质子交换器,属于负责摄取白蛋白和低分子量蛋白质的内吞大分子复合物。研究发现,在肾小球肾炎的肾小球以及白蛋白过载条件下培养的人足细胞中,ClC-5均过表达。目前对人ClC-5的转录调控尚未完全了解。在人肾脏中检测到了三种不同强度的功能性启动子以及信使核糖核酸(mRNA)的11种不同的5'非翻译区(5'UTR)异构体(变体1-11)。本研究的目的是调查5种5'UTR变体和共同翻译区在肾小球肾炎中的表达模式。使用定量相对实时PCR或定量比较终点PCR,以作为看家基因,对8个正常肾脏和12例肾小球肾炎患者的肾活检组织中mRNA的5'UTR末端和翻译区进行了分析。正常和肾小球肾炎活检组织中所有变体的表达谱相似,变体3和替代变体4在两组中表达最为丰富。在肾小球肾炎活检组织中,受弱启动子调控的异构体(变体4、6和7)表达增加,导致翻译区增加,突出了它们在肾脏病理生理学中的重要性。由于弱启动子可被不同刺激激活,这些数据支持了蛋白尿可能是能够启动诱导转录增加的信号通路的刺激因素之一这一假说。