Proteome analysis of serum from type 2 diabetics with nephropathy

被引:66
作者
Kim, Hyun-Jung [1 ]
Cho, Eun-Hee [1 ]
Yoo, Ji-Hye [1 ]
Kim, Pan-Kyeom [1 ]
Shin, Jun-Seop [1 ]
Kim, Mi-Ryung [1 ]
Kim, Chan-Wha [1 ]
机构
[1] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
关键词
serum; diabetic nephropathy; 2-DE; eGPx; ApoE; ESI-Q-TOF MS/MS;
D O I
10.1021/pr060489g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic nephropathy (DN) is a renal disease which develops as a consequence of diabetes mellitus. Microalbuminuria is the earliest clinical sign of DN. There are no specific diagnostic biomarkers for type 2 diabetics with nephropathy other than microalbuminuria and macroalbuminuria. However, microalbuminuria does not constitute a sole independent indicator for type 2 diabetics with nephropathy, and thus, another screening method, such as a biomarker assay, is required in order to diagnose it more correctly. Therefore, we have utilized two-dimensional electrophoresis (2-DE) to identify human serum protein markers for the more specific and accurate prediction of progressive nephropathy in type 2 diabetes patients, via comparisons of the serum proteome in three experimental groups: type 2 diabetes patients without microalbuminuria (DM, n = 30), with microalbuminuria (MA, n = 29), and with chronic renal failure (CRF, n = 31). As a result, proteins which were differentially expressed with statistical significance (p < 0.05) in MA and CRF groups as compared to those in DM group were selected and identified by ESI-Q-TOF MS/MS. Among these identified proteins, two proteins which might be useful as diagnostic biomarkers of type 2 diabetics with nephropathy were verified by Western blotting: extracellular glutathione peroxidase (eGPx) and apolipoprotein (ApoE) were found to exhibit a progressive reduction in MA and CRF groups. Notably, eGPx was further verified by ELISA using DM (n = 100) and MA (n = 96) patient samples. Collectively, our results show that the two proteins identified in this study may constitute potential biomarkers for the diagnosis of type 2 diabetics with nephropathy.
引用
收藏
页码:735 / 743
页数:9
相关论文
共 54 条
[1]   Development and progression of nephropathy in type 2 diabetes: The United Kingdom Prospective Diabetes Study (UKPDS 64) [J].
Adler, AI ;
Stevens, RJ ;
Manley, SE ;
Bilous, RW ;
Cull, CA ;
Holman, RR .
KIDNEY INTERNATIONAL, 2003, 63 (01) :225-232
[2]  
Araki T, 1998, J NEUROSCI RES, V53, P7, DOI 10.1002/(SICI)1097-4547(19980701)53:1<7::AID-JNR2>3.0.CO
[3]  
2-F
[4]   HUMAN KIDNEY PROXIMAL TUBULES ARE THE MAIN SOURCE OF PLASMA GLUTATHIONE-PEROXIDASE [J].
AVISSAR, N ;
ORNT, DB ;
YAGIL, Y ;
HOROWITZ, S ;
WATKINS, RH ;
KERL, EA ;
TAKAHASHI, K ;
PALMER, IS ;
COHEN, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02) :C367-C375
[5]  
Aymerich MS, 2001, INVEST OPHTH VIS SCI, V42, P3287
[6]   Prevention of loss of renal function over time in patients with diabetic nephropathy [J].
Barnett, A .
AMERICAN JOURNAL OF MEDICINE, 2006, 119 (05) :40S-47S
[7]  
BENNETT PH, 1995, AM J KIDNEY DIS, V25, P107
[8]  
Bilak MM, 2002, J NEUROSCI, V22, P9378
[9]   Interleukin-6 predicts hypoalbuminemia, hypocholesterolemia, and mortality in hemodialysis patients [J].
Bologa, RM ;
Levine, DM ;
Parker, TS ;
Cheigh, JS ;
Serur, D ;
Stenzel, KH ;
Rubin, AL .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (01) :107-114
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3