Mechanism of hypoxia-induced damage to the mechanical property in human erythrocytes-band 3 phosphorylation and sulfhydryl oxidation of membrane proteins

被引:1
|
作者
Yang, Qinqin [1 ]
Chen, Dong [1 ]
Li, Chungong [1 ]
Liu, Runjing [1 ]
Wang, Xiang [1 ]
机构
[1] Chongqing Univ, Coll Bioengn, Key Lab Biorheol Sci & Technol, Minist Educ, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
resveratrol; band; 3; crosslinking; hypoxia; phosphorylation; erythrocyte deformability; TYROSINE PHOSPHORYLATION; KINASE-C; RESVERATROL; DEFORMABILITY; STRESS; WINE; RESPONSES; OXIDASE; MARKERS; STORAGE;
D O I
10.3389/fphys.2024.1399154
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Introduction: The integrity of the erythrocyte membrane cytoskeletal network controls the morphology, specific surface area, material exchange, and state of erythrocytes in the blood circulation. The antioxidant properties of resveratrol have been reported, but studies on the effect of resveratrol on the hypoxia-induced mechanical properties of erythrocytes are rare.Methods: In this study, the effects of different concentrations of resveratrol on the protection of red blood cell mor-phology and changes in intracellular redox levels were examined to select an appropriate concentration for further study. The Young's modulus and surface roughness of the red blood cells and blood viscosity were measured via atomic force microsco-py and a blood rheometer, respectively. Flow cytometry, free hemoglobin levels, and membrane lipid peroxidation levels were used to characterize cell membrane damage in the presence and absence of resveratrol after hypoxia. The effects of oxida-tive stress on the erythrocyte membrane proteins band 3 and spectrin were further investigated by immunofluorescent label-ing and Western blotting.Results and discussion: Resveratrol changed the surface roughness and Young's modulus of the erythrocyte mem-brane, reduced the rate of eryptosis in erythrocytes after hypoxia, and stabilized the intracellular redox level. Further data showed that resveratrol protected the erythrocyte membrane proteins band 3 and spectrin. Moreover, resistance to band 3 pro-tein tyrosine phosphorylation and sulfhydryl oxidation can protect the stability of the erythrocyte membrane skeleton net-work, thereby protecting erythrocyte deformability under hypoxia. The results of the present study may provide new insights into the roles of resveratrol in the prevention of hypoxia and as an antioxidant.
引用
收藏
页数:14
相关论文
共 5 条
  • [1] Nitric oxide inhibits hypoxia-induced impairment of human RBC deformability through reducing the cross-linking of membrane protein band 3
    Zhao, Yajin
    Wang, Xiang
    Wang, Ruofeng
    Chen, Dong
    Noviana, Milody
    Zhu, Hongliang
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (01) : 305 - 320
  • [2] Modifications of band 3 and oxidation level of membrane proteins in senescent erythrocytes
    Rucci, Angel
    Alejandra Ensinck, Maria
    Mufarrege, Nicolas
    Cotorruelo, Carlos
    Garcia Borras, Silvia
    Racca, Liliana
    Biondi, Claudia
    Racca, Amelia
    CLINICAL BIOCHEMISTRY, 2010, 43 (13-14) : 1171 - 1173
  • [3] Peroxynitrite signaling in human erythrocytes: Synergistic role of hemoglobin oxidation and band 3 tyrosine phosphorylation
    Metere, Alessio
    Iorio, Egidio
    Pietraforte, Donatella
    Podo, Franca
    Minetti, Maurizio
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 484 (02) : 173 - 182
  • [4] Particle Simulation of Oxidation Induced Band 3 Clustering in Human Erythrocytes
    Shimo, Hanae
    Arjunan, Satya Nanda Vel
    Machiyama, Hiroaki
    Nishino, Taiko
    Suematsu, Makoto
    Fujita, Hideaki
    Tomita, Masaru
    Takahashi, Koichi
    PLOS COMPUTATIONAL BIOLOGY, 2015, 11 (06)
  • [5] Mancozeb-induced cytotoxicity in human erythrocytes: enhanced generation of reactive species, hemoglobin oxidation, diminished antioxidant power, membrane damage and morphological changes
    Quds, Ruhul
    Iqbal, Zarmin
    Arif, Amin
    Mahmood, Riaz
    PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2023, 193