Proteomic analysis of rat plasma with experimental autoimmune uveitis based on label-free liquid chromatography-tandem mass spectrometry (LC-MS/MS)

被引:9
作者
Guo, Dadong [1 ,2 ,3 ]
Gu, Peiming [4 ]
Liu, Zhengfeng [5 ]
Tang, Kai [5 ]
Du, Yuxiang [5 ]
Bi, Hongsheng [1 ,2 ,3 ]
机构
[1] Shandong Prov Key Lab Integrated Tradit Chinese &, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Key Lab Integrated Tradit Chinese & Western Med P, Jinan, Shandong, Peoples R China
[3] Shandong Univ Tradit Chinese Med, Inst Eye, Jinan 250002, Peoples R China
[4] Thermo Fisher Sci Shanghai, Shanghai 201206, Peoples R China
[5] Shandong Univ Tradit Chinese Med, Jinan, Shandong, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 976卷
基金
中国国家自然科学基金;
关键词
Experimental autoimmune uveitis; Rat; Mass spectrometry; Proteomics; Plasma; ENDOTOXIN-INDUCED UVEITIS; UVEORETINITIS; EXPRESSION; INDUCTION; CYTOKINES; ALPHA; IL-21; MICE; EAU;
D O I
10.1016/j.jchromb.2014.11.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Uveitis is a severe autoimmune eye disease that can cause intraocular inflammation even lead to severe vision loss, and the occurrence of uveitis can be closely associated with abnormal expression of proteins. However, the abnormally expressed proteins involved in uveitis are not well identified. Using liquid chromatography-tandem mass spectrometry technique, we examined the alterations in proteomic expression profiling in rat plasma specimens related to experimental autoimmune uveitis (EAU) versus normal samples. In addition, the experimental verification was further performed using enzyme-linked immunosorbent assay (ELISA) for abnormally expressed proteins in EAU rat plasma. The results indicate that 62 proteins were upregulated and 106 proteins were downregulated in plasma from EAU rats compared with those in saline-treated samples. In the meantime, we observed that the plasma level of complement component 3 in EAU rats was upregulated versus saline-treated rats (from 92.32 mu g/mL to 168.92 mu g/mL), whereas the level of interleukin-1 receptor accessory protein was downregulated (from 1120.97 pg/mL to 798.39 pg/mL), and these results were highly in agreement with those of mass spectrometry determination. Taken together, our results indicate that liquid chromatography-tandem mass spectrometry analysis possesses a good resolution for peptides in plasma, and the findings will provide the baseline plasma dataset for EAU rats and the relevant information can contribute to future studies on the understanding the mechanism of uveitis. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 90
页数:7
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