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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Dynamics of absolute amount of nephrin in a single podocyte in puromycin aminonucleoside nephrosis rats calculated by quantitative glomerular proteomics approach with selected reaction monitoring mode
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Dynamics of absolute amount of nephrin in a single podocyte in puromycin aminonucleoside nephrosis rats calculated by quantitative glomerular proteomics approach with selected reaction monitoring mode

机译:定量肾小球蛋白质组学方法选择反应监测模式计算嘌呤霉素氨基核苷肾病大鼠单足细胞中肾素绝对量的动力学

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摘要

Background. The slit diaphragm (SD) is a complex of podocyte-specific proteins and plays a significant role in glomerular filtration. To understand podocyte biology, it is important to determine the expression amount of the SD complex proteins. This study aimed to quantify the absolute amount of nephrin, which is believed to be a major component of SD, in podocytes and to apply that method to normal and puromycin aminonucleoside (PAN) nephrosis rats. Methods. The counting method for podocyte number in a glomerulus was developed by three-dimensional reconstruction imaging of Wilms tumor (WT-1) immunofluorescence on isolated glomeruli. Absolute amount of nephrin was quantified by mass spectrometry using the selected reaction monitoring (SRM) mode with a stable isotope-labeled peptide. Results. The number of podocytes per glomerulus was 95.5 ± 17.6 in the control rats, 90.7 ± 19.2 on Day 4 and 90.7 ± 26.2 on Day 7 in PAN nephrosis rats. The amount of nephrin per glomerulus in control rats was 1.02 ± 0.11 fmol and those in PAN nephrosis rats were reduced to 0.46 ± 0.06 fmol and 0.35 ± 0.04 fmol on Day 4 and Day 7. The nephrin amount per podocyte was significantly decreased association with the development of proteinuria in PAN nephrosis rats. Conclusions. This study established the absolute quantification of nephrin and determined the amount of nephrin in a podocyte of normal and PAN nephrosis rat kidneys. This highly sensitive and selective quantification method for protein is a useful tool for the analysis of SD protein in a podocyte.
机译:背景。裂隙隔膜(SD)是足细胞特异性蛋白质的复合物,在肾小球滤过中起重要作用。为了了解足细胞生物学,重要的是确定SD复合蛋白的表达量。这项研究的目的是量化足细胞中肾素的绝对数量,肾素被认为是SD的主要成分,并将该方法应用于正常和嘌呤霉素氨基核苷(PAN)肾病大鼠。方法。通过对孤立肾小球上的Wilms肿瘤(WT-1)免疫荧光进行三维重建成像,开发了肾小球足细胞数的计数方法。使用选定的反应监测(SRM)模式和稳定的同位素标记的肽,通过质谱法对肾素的绝对量进行定量。结果。在对照大鼠中,每只肾小球的足细胞数为95.5±17.6,在PAN肾病大鼠中,在第4天为90.7±19.2,在第7天为90.7±26.2。在第4天和第7天,对照大鼠的肾小球中肾素的量为1.02±0.11 fmol,PAN肾病大鼠中的肾小球中的nephrin量减少至0.46±0.06 fmol和0.35±0.04 fmol。肾病大鼠蛋白尿的发生结论这项研究建立了肾素的绝对定量,并测定了正常和PAN肾病大鼠肾脏足细胞中的肾素含量。这种蛋白质的高灵敏度和选择性定量方法是分析足细胞中SD蛋白质的有用工具。

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