Membrane Skeletal Protein S-Glutathionylation in Human Red Blood Cells as Index of Oxidative Stress

被引:16
|
作者
Giustarini, Daniela [1 ]
Dalle-Donne, Isabella [2 ]
Milzani, Aldo [2 ]
Braconi, Daniela [1 ]
Santucci, Annalisa [1 ]
Rossi, Ranieri [1 ]
机构
[1] Univ Siena, Dept Biotechnol Chem & Pharm, Dept Excellence 2018 2022, Via A Moro 2, I-53100 Siena, Italy
[2] Univ Milan, Dept Biosci, Dept Excellence 2018 2022, Via Celoria 26, I-20133 Milan, Italy
关键词
GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; HEMOGLOBIN; BIOMARKERS; DISULFIDE; ERYTHROCYTES; QUANTITATION; SPECTRIN;
D O I
10.1021/acs.chemrestox.8b00408
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glutathione (GSH) is one of the most well-studied biomarkers of oxidative stress. Under oxidizing conditions, GSH is transformed into its disulfide forms, glutathione disulfide (GSSG) and S-glutathionylated proteins (PSSG), which are considered to be reliable biomarkers of oxidative stress. In red blood cells (RBCs), the main targets of S-glutathionylation are hemoglobin and membrane-associated skeletal proteins, but S-glutathionylated hemoglobin (HbSSG) has been more thoroughly studied as a biomarker of oxidative stress than S-glutahionylated RBC membrane skeletal proteins. Here, we have investigated whether and how all these biomarkers are altered in human RBCs treated with a slow and cyclically intermittent flux of the oxidant tert-butyl hydroperoxide. To this aim, a new device for sample treatment and collection was developed. During and at the end of the treatment, GSH, GSSG, and PSSG (discriminating between HbSSG and membrane PSSG) were measured by the use of spectrophotometer (for GSSG) and HPLC (for GSH, HbSSG, and membrane PSSG). The main results of our study are as follows: (i) GSH decreased and GSSG increased, but only in the presence of the oxidant, and recovered their initial values at the end of the infusion; (ii) the increase in total PSSG concentration was lower than that of GSSG, but it kept on throughout the experiments; (iii) membrane skeletal proteins did not recover their initial values, whereas HbSSG levels recovered their initial values similarly to GSH and GSSG; (d) membrane skeletal PSSG were more stable and also more abundant than HbSSG. Western blot analysis indicated spectrin, ankyrin, and bands 3, 4.1, and 4.2 as the proteins most susceptible to S-glutathionylation in RBC membrane. These results suggest that S-glutathionylated membrane skeletal proteins can be considered as a suitable biomarker of oxidative stress. Mostly when the oxidant insult is slight and intermittent, PSSG in RBC membranes are worth measuring in addition to GSSG by virtue of their greater stability.
引用
收藏
页码:1096 / 1102
页数:7
相关论文
共 50 条
  • [1] Membrane skeletal protein S-glutathionylation and hemolysis in human red blood cells
    Rossi, Ranieri
    Giustarini, Daniela
    Milzani, Aldo
    Dalle-Donne, Isabella
    BLOOD CELLS MOLECULES AND DISEASES, 2006, 37 (03) : 180 - 187
  • [2] S-Glutathionylation of metallothioneins by nitrosative/oxidative stress
    Casadei, Manuela
    Persichini, Tiziana
    Polticelli, Fabio
    Musci, Giovanni
    Colasanti, Marco
    EXPERIMENTAL GERONTOLOGY, 2008, 43 (05) : 415 - 422
  • [3] Protein S-glutathionylation in human platelets
    Giustarini, D
    Dalle-Donne, I
    Aldini, G
    Ceciliani, F
    Colombo, R
    Milzani, A
    Rossi, R
    FASEB JOURNAL, 2005, 19 (04): : A817 - A817
  • [4] Oxidative Stress Promotes Protein Tyrosine Nitration and S-Glutathionylation Impairing Motility and Capacitation in Human Spermatozoa
    Morielli, Tania
    O'Flaherty, Cristian
    FREE RADICAL BIOLOGY AND MEDICINE, 2012, 53 : S137 - S137
  • [5] Stress-induced protein S-glutathionylation in Arabidopsis
    Dixon, DP
    Skipsey, M
    Grundy, NM
    Edwards, R
    PLANT PHYSIOLOGY, 2005, 138 (04) : 2233 - 2244
  • [6] Oxidative Stress Inhibits Vascular KATP Channels by S-Glutathionylation
    Yang, Yang
    Shi, Weiwei
    Cui, Ningren
    Wu, Zhongying
    Jiang, Chun
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (49) : 38641 - 38648
  • [7] Interplay among Oxidative Stress, Methylglyoxal Pathway and S-Glutathionylation
    de Bari, Lidia
    Scire, Andrea
    Minnelli, Cristina
    Cianfruglia, Laura
    Kalapos, Miklos Peter
    Armeni, Tatiana
    ANTIOXIDANTS, 2021, 10 (01) : 1 - 17
  • [8] S-Glutathionylation Enhances Human Cystathionine β-Synthase Activity Under Oxidative Stress Conditions
    Niu, Wei-Ning
    Yadav, Pramod Kumar
    Adamec, Jiri
    Banerjee, Ruma
    ANTIOXIDANTS & REDOX SIGNALING, 2015, 22 (05) : 350 - 361
  • [9] Evidence by chromatography and mass spectrometry that inorganic nitrite induces S-glutathionylation of hemoglobin in human red blood cells
    Boehmer, Anke
    Pich, Andreas
    Schmidt, Mario
    Haghikia, Arash
    Tsikas, Dimitrios
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2016, 1019 : 72 - 82
  • [10] S-Glutathionylation of buccal mucosal cell proteins as biomarkers of oxidative stress
    Grek, Christina L.
    Manevich, Yefim
    Townsend, Danyelle M.
    Tew, Kenneth D.
    CANCER RESEARCH, 2013, 73 (08)