Oxidative stress causes membrane phospholipid rearrangement and shedding from RBC membranes-An NMR study

被引:41
作者
Freikman, Inna [2 ]
Amer, Johnny [1 ]
Cohen, Jack S. [2 ]
Ringel, Israel [2 ]
Fibach, Eitan [1 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr, Dept Hematol, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Sch Pharm, Dept Pharmacol, IL-91905 Jerusalem, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2008年 / 1778卷 / 10期
关键词
Membrane phospholipids; Oxidative stress; Thalassemia; RBC; NMR;
D O I
10.1016/j.bbamem.2008.06.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear Magnetic Resonance (NMR) spectroscopy was used to investigate the relationship between oxidative stress experienced by RBCs and their phospholipid content and shedding. Using H-1-NMR, we demonstrated a higher lactate/pyruvate ratio, an indicator of oxidative stress, in normal RBCs treated with oxidants (t-butylhydroxyperoxide and H2O2) as well as in beta-thalassemic RBCs. Using P-31-NMR, we found 30% more phosphatidylcholine (PC), and unexpectedly, 35% less phosphatidylserine (PS) in the thalassemic RBCs. PS was decreased by treatment with oxidants and increased by anti-oxidants (vitamin C and N-acetyl cysteine); PC showed the opposite behavior. Thalassemic RBCs incubated in phosphate buffered saline produced more PS in the supernatant than normal RBCs. Anti-oxidants reduced the PS in the supernatant while oxidants increased it. Plasma of thalassemic patients contained 2.6-fold and 1.8-fold more PS and PC, respectively, than normal plasma. These results indicate that the decreased PS in RBCs resulted from increased shedding. The nature of the shed PS was studied by purifying and analyzing membranous microparticles from the plasma and RBC supernatants. More PS was found in microparticles purified from thalassemic plasma and RBC supernatants (5.6- and 4.8-fold, respectively) than in their normal counterparts. However, the bulk (80-90%) of the shed PS was not associated with microparticles. The significance of PS shedding for RBC survival needs further clarification. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2388 / 2394
页数:7
相关论文
共 46 条
[1]   Oxidative status of platelets in normal and thalassemic blood [J].
Amer, J ;
Fibach, E .
THROMBOSIS AND HAEMOSTASIS, 2004, 92 (05) :1052-1059
[2]   Flow cytometric analysis of the oxidative status of normal and thalassemic red blood cells [J].
Amer, J ;
Goldfarb, A ;
Fibach, E .
CYTOMETRY PART A, 2004, 60A (01) :73-80
[3]   N-acetylcysteine amide (AD4) attenuates oxidative stress in beta-thalassemia blood cells [J].
Amer, Johnny ;
Atlas, Daphne ;
Fibach, Eitan .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (02) :249-255
[4]  
BORENSTAINBENYASHAR V, 1993, AM J HEMATOL, V44, P63
[5]   Antioxidant defense status of red blood cells of patients with β-thalassemia and Eβ-thalassemia [J].
Chakraborty, D ;
Bhattacharyya, M .
CLINICA CHIMICA ACTA, 2001, 305 (1-2) :123-129
[6]   Interaction of antioxidants and their implication in genetic anemia [J].
Chan, AC ;
Chow, CK ;
Chiu, D .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 222 (03) :274-282
[7]   Apoptosis is associated with an inhibition of aminophospholipid translocase (APTL) in CNS-derived HN2-5 and HOG cells and phosphatidylserine is a recognition molecule in microglial uptake of the apoptotic HN2-5 cells [J].
Das, P ;
Estephan, R ;
Banerjee, P .
LIFE SCIENCES, 2003, 72 (23) :2617-2627
[8]   Biomarkers of free radical damage applications in experimental animals and in humans [J].
De Zwart, LL ;
Meerman, JHN ;
Commandeur, JNM ;
Vermeulen, NPE .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (1-2) :202-226
[9]   The hypercoagulable state in thalassemia [J].
Eldor, A ;
Rachmilewitz, EA .
BLOOD, 2002, 99 (01) :36-43
[10]   Differences in platelet growth factor release and leucocyte kinetics during autologous platelet gel formation [J].
Everts, P. A. M. ;
Hoffmann, J. ;
Weibrich, G. ;
Mahoney, C. B. ;
Schonberger, J. P. A. M. .
TRANSFUSION MEDICINE, 2006, 16 (05) :363-368