Comparative proteomic analysis of renal tissue in IgA nephropathy with iTRAQ quantitative proteomics

被引:8
|
作者
Sui, Weiguo [1 ]
Cui, Zhenzhen [1 ,2 ]
Zhang, Ruohan [1 ]
Xue, Wen [1 ]
Ou, Minglin [1 ]
Zou, Guimian [1 ]
Chen, Jiejing [1 ]
Dai, Yong [3 ]
机构
[1] 181st Hosp, Guangxi Key Lab Metab Dis Res, Nephrol Dept, Guilin 541002, Guangxi, Peoples R China
[2] Guangxi Normal Univ, Life Sci Coll, Guilin 541004, Guangxi, Peoples R China
[3] Jinan Univ, Shenzhen Peoples Hosp, Clin Med Coll 2, Clin Med Res Ctr, 1017 Dong Min Bei Lu, Shenzhen 518020, Guangdong, Peoples R China
关键词
isobaric tags for relative and absolute quantification technology; immunoglobulin A nephropathy; proteomic; tandem mass spectrometry;
D O I
10.3892/br.2014.318
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Immunoglobulin (Ig) A nephropathy (IgAN) is the most common form of glomerulonephritis. In clinical practice, it is difficult to monitor the repeating relapse in patients suffering from IgAN, which usually occurs within 10 years of end-stage renal disease. In order to identify and quantify the total protein content in the renal tissue of patients with IgAN, isobaric tags for relative and absolute quantification (iTRAQ) technology was performed. iTRAQ coupled with multiple chromatographic fractionation and tandem mass spectrometry was used to analyze the total protein of normal renal tissue in IgAN and healthy patients. The individual proteins were identified by the Mascot search engine and any that were differentially expressed were monitored. A total of 574 different proteins were identified, and 287 proteins were up-or downregulated by >1 fold alteration in levels. The results showed that iTRAQ-based quantitative proteomic technology for the identification and relative quantitation of the renal tissue proteome is efficiently applicable. The differential expression of the proteome profiles for IgAN patients was determined. Further studies using large cohorts of patient samples with long-term clinical follow-up data should be conducted to evaluate the usefulness of the pathogenesis and novel biomarker candidates of IgAN, which may develop a novel technique for the diagnosis of IgAN.
引用
收藏
页码:793 / 798
页数:6
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