Elevation of apolipoprotein A-I and apolipoprotein H levels in the vitreous fluid and overexpression in the retina of diabetic patients

被引:70
作者
Simo, Rafael [1 ,2 ]
Higuera, Monica [1 ]
Garcia-Ramirez, Marta [1 ,2 ]
Canals, Francesc [3 ]
Garcia-Arumi, Jose [4 ]
Hernandez, Cristina [1 ,2 ]
机构
[1] Univ Autonoma Barcelona, Inst Recerca Hosp Univ Vall Hebron, Diabet Res Unit, Barcelona 08035, Spain
[2] Univ Autonoma Barcelona, Inst Recerca Hosp Univ Vall Hebron, CIBERdem, Barcelona 08035, Spain
[3] Univ Autonoma Barcelona, Inst Recerca Hosp Univ Vall Hebron, Med Oncol Res Program, Prote Lab, Barcelona 08035, Spain
[4] Univ Autonoma Barcelona, Inst Recerca Hosp Univ Vall Hebron, Dept Ophthalmol, Barcelona 08035, Spain
关键词
D O I
10.1001/archopht.126.8.1076
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objectives: To determine levels of apolipoprotein (apo) A-I and apo H in the vitreous fluid of patients with proliferative diabetic retinopathy (PDR) and to examine whether apo A-I and apo H messenger RNA (mRNA) levels are overexpressed in the diabetic retina. Methods: Vitreous samples from 4 diabetic patients with PDR and 8 nondiabetic patients with macular hole were selected for proteomic analysis. Fourteen additional samples (7 from patients with PDR and 7 from patients with macular hole) were used for Western blot analysis. Fourteen postmortem eyes (7 from diabetic and 7 from nondiabetic donors) were used to perform quantitative real-time polymerase chain reaction analysis. Results: Intravitreous apo A-I and apo H levels were significantly higher in patients with PDR than in the control group. The apo A-I and apo H mRNA levels obtained from the retinas of diabetic donors were significantly higher than those obtained from nondiabetic donors. Retinal pigment epithelium was the main contributor to the differences. Conclusions: Levels of apo A-I and apo H are elevated in the vitreous fluid of diabetic patients with PDR. In addition, we provide the first evidence, to our knowledge, that a higher expression of apo A-I and apo H mRNAs exists in the diabetic retina. Clinical Relevance: The results of this study may be relevant to new treatment strategies aimed toward reducing the development of diabetic retinopathy.
引用
收藏
页码:1076 / 1081
页数:6
相关论文
共 40 条
[1]   A novel experimental design for comparative two-dimensional gel analysis: Two-dimensional difference gel electrophoresis incorporating a pooled internal standard [J].
Alban, A ;
David, SO ;
Bjorkesten, L ;
Andersson, C ;
Sloge, E ;
Lewis, S ;
Currie, I .
PROTEOMICS, 2003, 3 (01) :36-44
[2]   Recruitment of beta-2-glycoprotein 1 to cell surfaces in extrinsic and intrinsic apoptosis [J].
Balasubramanian, K ;
Maiti, SN ;
Schroit, AJ .
APOPTOSIS, 2005, 10 (02) :439-446
[3]   COMPLETE PRIMARY STRUCTURE OF BOVINE BETA-2-GLYCOPROTEIN .1. LOCALIZATION OF THE DISULFIDE BRIDGES [J].
BENDIXEN, E ;
HALKIER, T ;
MAGNUSSON, S ;
SOTTRUPJENSEN, L ;
KRISTENSEN, T .
BIOCHEMISTRY, 1992, 31 (14) :3611-3617
[4]   BETA-2-GLYCOPROTEIN-I IS A MAJOR PROTEIN ASSOCIATED WITH VERY RAPIDLY CLEARED LIPOSOMES IN-VIVO, SUGGESTING A SIGNIFICANT ROLE IN THE IMMUNE CLEARANCE OF NON-SELF PARTICLES [J].
CHONN, A ;
SEMPLE, SC ;
CULLIS, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) :25845-25849
[5]   Serum apolipoprotein H and its relationship to blood pressure, serum lipids, fasting plasma glucose and insulin in normal individuals [J].
Crook, M ;
Ch'ng, SI ;
Lumb, P ;
Reid, F .
ANNALS OF CLINICAL BIOCHEMISTRY, 2001, 38 :494-498
[6]  
Curcio CA, 2001, INVEST OPHTH VIS SCI, V42, P265
[7]   EXPRESSION OF RAT APOLIPOPROTEIN-A-IV AND APOLIPOPROTEIN-A-I GENES - MESSENGER-RNA INDUCTION DURING DEVELOPMENT AND IN RESPONSE TO GLUCOCORTICOIDS AND INSULIN [J].
ELSHOURBAGY, NA ;
BOGUSKI, MS ;
LIAO, WSL ;
JEFFERSON, LS ;
GORDON, JI ;
TAYLOR, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (23) :8242-8246
[8]  
FAIRBANKS VF, 1992, CLIN CHEM, V38, P132
[9]   Proteomic analysis of human vitreous fluid by fluorescence-based difference gel electrophoresis (DIGE):: a new strategy for identifying potential candidates in the pathogenesis of proliferative diabetic retinopathy [J].
Garcia-Ramirez, M. ;
Canals, F. ;
Hernandez, C. ;
Colome, N. ;
Ferrer, C. ;
Carrasco, E. ;
Garcia-Arumi, J. ;
Simo, R. .
DIABETOLOGIA, 2007, 50 (06) :1294-1303
[10]  
Gerl VB, 2002, INVEST OPHTH VIS SCI, V43, P1104