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利用定量肾小球蛋白质组学方法结合选择反应监测模式计算嘌呤霉素氨基核苷肾病大鼠单个足细胞中nephrin 的绝对量的动态变化。

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.

机构信息

Laboratory of Veterinary Pathology, Faculty of Veterinary Medicine, Azabu University, Sagamihara, Japan.

出版信息

Nephrol Dial Transplant. 2012 Apr;27(4):1324-30. doi: 10.1093/ndt/gfr492. Epub 2011 Aug 22.

DOI:10.1093/ndt/gfr492
PMID:21862459
Abstract

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.

摘要

背景

裂孔隔膜(SD)是足细胞特异性蛋白的复合物,在肾小球滤过中起着重要作用。为了了解足细胞生物学,确定 SD 复合物蛋白的表达量是很重要的。本研究旨在定量检测认为是 SD 的主要成分之一的nephrin 的绝对量,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

通过对分离的肾小球进行 WT-1 免疫荧光的三维重建成像,开发了肾小球内足细胞数量的计数方法。采用稳定同位素标记肽的选择反应监测(SRM)模式,通过质谱法对 nephrin 的绝对量进行定量。

结果

对照组大鼠每个肾小球的足细胞数为 95.5±17.6,PAN 肾病大鼠第 4 天和第 7 天分别为 90.7±19.2 和 90.7±26.2。对照组大鼠每个肾小球的 nephrin 量为 1.02±0.11 fmol,PAN 肾病大鼠第 4 天和第 7 天分别减少至 0.46±0.06 fmol 和 0.35±0.04 fmol。与 PAN 肾病大鼠蛋白尿的发展相关,nephrin 量/足细胞显著减少。

结论

本研究建立了 nephrin 的绝对定量,并确定了正常和 PAN 肾病大鼠肾脏中足细胞内 nephrin 的量。这种对蛋白质具有高度灵敏和选择性的定量方法是分析足细胞中 SD 蛋白的有用工具。

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