Anion exchanger and the resistance against thermal haemolysis

References

• Lang F, Lang KS, Lang PA, Huber SM, Wieder T. Mechanisms and significance of eryptosis. Antioxid Redox Signal 2006; 8: 1183–1192
   PubMed Web of Science ®Google Scholar
• Coakley WT, Bater AJ, Crum LA, Deeley JOT. Morphological changes, haemolysis and microvesiculation of heated human erythrocytes. J Therm Biol 1979; 4: 85–95
   Web of Science ®Google Scholar
• Juckett DA, Rosenberg B. The kinetics and thermodynamics of lysis of young and old sheep red blood cells. Mech Ageing Dev 1982; 18: 33–45
   PubMedGoogle Scholar
• Gershfeld RE, Murayama M. Thermal instability of red blood cell membrane bilayers: Temperature dependence of thermohaemolysis. J Membr Biol 1988; 101: 67–72
   PubMed Web of Science ®Google Scholar
• Chernitskii EA, Iamaikina I. Thermohaemolysis of erythrocytes. Biofizika 1988; 33: 319–322, (in Russian)
   PubMedGoogle Scholar
• Lepock JR, Frey HE, Bayne H, Markus J. Relationship of hyperthermia-induced hemolysis of human erythrocytes to the thermal denaturation of membrane proteins. Biochim Biophys Acta 1989; 980: 191–201
   PubMed Web of Science ®Google Scholar
• Iamaikina IV, Chernitskii EA. Denaturation of hemoglobin – The first stage of erythrocyte thermohemolysis. Biofizika 1989; 34: 656–659, (in Russian)
   PubMedGoogle Scholar
• Coakley WT, Owen J, Deeley T. Effects of ionic strength, serum protein and surface charge on membrane movements and vesicle production in heated erythrocytes. Biochim Biophys Acta 1980; 602: 355–375
   PubMedGoogle Scholar
• Prinsze C, Tijssen K, Dubbelman TM, Van Stevenick J. Potentiation of hyperthermia-induced haemolysis of human erythrocytes by photodynamic treatment. Evidence for the involvement of the anion transporter in this synergistic interaction. Biochem J 1991; 277: 183–188
   PubMedGoogle Scholar
• Marton LS, Garvin LE. Subunit structure of the major human erythrocytes glycoprotein: Depolymerization by heating ghosts with sodium dodecyl sulphate. Biochem Biophys Res Commun 1973; 52: 1457–1462
   PubMedGoogle Scholar
• Brandts JF, Erickson L, Lysko K, Schwartz AT, Taverna RD. Calorimetric studies of the structural transitions of the human erythrocyte membrane. The involvement of spectrin in the A transition. Biochemistry 1977; 16: 3450–3454
   PubMed Web of Science ®Google Scholar
• Snow JW, Brandts JF, Low PS. The effects of anion transport inhibitors on the structural transitions in erythrocyte membranes. Biochim Biophys Acta 1978; 512: 579–591
   PubMedGoogle Scholar
• Ivanov IT, Benov LC. Thermohemolysis of human erythrocytes in isotonic NaCl/sucrose media during transient heating. J Therm Biology 1992; 17: 381–389
   Web of Science ®Google Scholar
• Ivanov IT. Thermohaemolysis of human erythrocytes in sucrose containing isotonic media. J Therm Biol 1992; 17: 375–379
   Web of Science ®Google Scholar
• Iamaikina IV, Chernitskii EA. Possible role of spectrin in thermohemolysis of erythrocytes. Biofizika 1988; 33: 626–628, (in Russian)
   PubMedGoogle Scholar
• Borisova AB, Goryunov AS. Thermal hemolysis of red blood cells differing in affinity of hemoglobin to oxygen. J Evol Biochem Physiol 1997; 33: 126–130
   Google Scholar
• Ivanov IT, Brähler M, Georgieva R, Bäumler H. Role of membrane proteins in thermal damage and necrosis of red blood cells. Thermochim Acta 2007; 456: 7–12
   Google Scholar
• Alper SL. The band 3-related anion exchanger (AE) gene family. Annu Rev Physiol 1991; 53: 549–564
   PubMed Web of Science ®Google Scholar
• Wilbrandt W. Osmotische Natur sogenannter nicht-osmotischer Hemolysen. (Kolloidosmotische Hemolyse), Arch Ges Physiol (Pflagers) 1941; 245: 22–52, [Wilbrandt W. Osmotic Nature of the so called not-osmotic Hemolysis. (Colloid-osmotic Hemolysis), Arch ges Physiol (Pflügers Arch) 1941;245:22–52]
   Google Scholar
• Ivanov IT. Thermohaemolysis of mammalian erythrocytes. J Therm Biol 1993; 18: 177–183
   Web of Science ®Google Scholar
• Ivanov IT. Allometric dependence of the life span of mammal erythrocytes on thermal stability and sphingomyelin content of plasma membranes. Comp Biochem Physiol Part A. 2007; 147: 876–884
   PubMedGoogle Scholar
• Back JF, Oakenfull D, Smith MB. Increased thermal stability of proteins by sugars and polyols. Biochemistry 1979; 18: 5191–5196
   PubMed Web of Science ®Google Scholar
• Santoro MM, Liu Y, Khan SM, Hou LX, Bolen DW. Increased thermal stability of proteins in the presence of naturally occurring osmolytes. Biochemistry 1992; 31: 5278–5283
   PubMed Web of Science ®Google Scholar
• Gordon J. The protective action of some amino-acids against the effect of heat on compliment. J Hyg 1953; 51: 140–144
   PubMedGoogle Scholar
• Li GC, Fisher GA, Hahn GM. Induction of thermotolerance and evidence for a well-defined thermotropic cooperative process. Radiat Res 1982; 89: 361–368
   PubMed Web of Science ®Google Scholar
• Alexandrov VYa. Cell Reactivity and Proteins. Science Publishing House, St Peterburg 1985
   Google Scholar
• Okoli CO, Akah PA. Mechanisms of the anti-inflammatory activity of the leaf extracts of Culcasia scandens P. Beauv (Araceae). Pharmacol Biochem Behav 2004; 79: 473–481
   PubMed Web of Science ®Google Scholar
• Cabantchik Z, Rothstein A. Membrane proteins related to anion permeability of human red blood cells. Localization of disulfonic stilbene binding sites in proteins involved in permeation. J Membr Biol 1974; 15: 207–226
   PubMed Web of Science ®Google Scholar
• Cabantchik ZI, Greger R. Chemical probes for anion transporters of mammalian cell membranes. Am J Physiol 1992; 262: C803–C827
   Google Scholar
• Macey R, Adorante JS, Orme FW. Erythrocyte membrane potentials determined by hydrogen ion distribution. Biochim Biophys Acta 1978; 512: 284–295
   PubMedGoogle Scholar
• Ivanov IT. Incorporation of sphingomyelin increases thermostability of human erythrocyte membrane and resistance of erythrocytes against thermal hemolysis. J Therm Biol 2002; 27: 285–289
   Google Scholar
• Ivanov IT. Impedance spectroscopy of human erythrocyte membrane: Effect of frequency at the spectrin denaturation transition temperature. Bioelectrochemistry 2010; 78: 181–185
   PubMedGoogle Scholar
• Hardin RB, Eakes DJ, Sibley JL, Gilliam CH, Keever GJ. Root membrane thermostability of Cornus florida L. provenances. J Therm Biol 1999; 24: 237–240
   Google Scholar
• Ivanov IT, Boytcheva S, Mihailova G. Parallel study of thermal resistance and permeability barrier stability of Enterococcus faecalis as affected by salt composition, growth temperature and pre-incubation temperature. J Therm Biol 1999; 24: 217–227
   Google Scholar
• Shortley G, Williams D. Elements of Physics5th. Prentice-Hall, Englewood Cliffs, NJ 1971; 534
   Google Scholar
• Kim JH. Modification of thermal effects: Chemical modifiers. Hyperthermia and Oncology. Thermal effects on cells and tissues, M Urano, EB Douple. VSP, Utrecht, Netherlands and TokyoJapan 1988; 1: 99–119
   Google Scholar
• Wenzel M. Protection of erythrocytes in D2O against damage by hyperthermy and freezing. J Clin Chem Clin Biochem 1976; 14: 185–188
   PubMedGoogle Scholar
• Lutz HU, von Däniken A, Semenza G, Bächi T. Glycophorin-enriched vesicles obtained by a selective extraction of human erythrocyte membranes with a non-ionic detergent. Biochim Biophys Acta 1979; 552: 262–280
   PubMedGoogle Scholar
• Wyse JW, Butterfield DA. Electron spin resonance and biochemical studies of the interaction of the polyamine, spermine, with the skeletal network of proteins in human erythrocyte membranes. Biochim Biophys Acta 1988; 941: 141–149
   PubMedGoogle Scholar
• Kłopocka J. Flow cytometric analysis of eosin-5-maleimide binding to protein of band 3 and Rh-related proteins in diagnosis of hereditary spherocytosis. New Medicine 2008; 1: 13–15
   Google Scholar
• Taylor AM, Zhu QS, Casey JR. Cysteine-directed cross-linking localizes regions of the human erythrocyte anion-exchange protein (AE1) relative to the dimeric interface. Biochem J 2001; 359: 661–668
   PubMedGoogle Scholar
• Corbett JD, Agre P, Palek J, Golan DE. Differential control of band 3 lateral and rotational mobility in intact red cells. J Clin Invest 1994; 94: 683–688
   PubMedGoogle Scholar
• Berliner LJ. The spin-labeled approach to labeling membrane protein sulfhydryl groups. Ann NY Acad Sci 1983; 414: 153–161
   PubMed Web of Science ®Google Scholar
• Jozwiak Z, Watała C. Changes induced by chlorpromazine and heat in erythrocyte membranes. J Therm Biol 1993; 18: 83–89
   Google Scholar
• Szwarocka A, Robak T, Krykowski E, Jozwiak Z. Interaction of anthracyclines with human erythrocytes at hyperthermic temperature. Int J Pharmaceutics 1996; 135: 167–176
   Google Scholar
• Wang YY, Li XJ, Xin WJ. Changes of the human erythrocyte membrane protein SH-binding site property with exposure to fluoride and three strong mutagens. Fluoride 1995; 28: 193–200
   Google Scholar
• Ivanov IT. Involvement of erythrocyte membrane proteins in temperature-induced disturbances of the permeability barrier. Membr Cell Biol 1997; 11: 45–56
   PubMedGoogle Scholar
• Maneri LR, Low PS. Structural stability of the erythrocyte membrane anion transporter, band 3, in different lipid environment. J Biol Chem 1988; 263: 16170–16178
   PubMedGoogle Scholar
• Sami M, Malik S, Watts A. Structural stability of the erythrocyte anion transporter, band 3, in native membranes and in detergent micelles. Biochim Biophys Acta 1992; 1105: 148–154
   PubMedGoogle Scholar
• Brandts JF, Taverna RD, Sadasivan E, Lysko KA. Calorimetric studies of the structural transitions of the human erythrocyte membrane. Studies of the B and C transitions. Biochim Biophys Acta 1978; 512: 566–578
   PubMedGoogle Scholar
• Senisterra GA, Lepock JR. Thermal destabilization of transmembrane proteins by local anaesthetics. Int J Hyperthermia 2000; 16: 1–17
   PubMedGoogle Scholar
• Zavodnik IB, Lapshina EA, Stepuro II. Thermostability of erythrocyte membrane in the presence of ethanol. Biofizika 1994; 39: 470–474, (in Russian)
   PubMedGoogle Scholar
• Miller TL, Smith RJ. Thermotropic properties of human erythrocyte membrane proteins as affected by hydroxychloroaromatic compounds. Arch Biochem Biophys 1986; 250: 128–138
   PubMedGoogle Scholar
• Ivanov IT. Investigation into the membrane alteration relevant to the mechanism of thermohaemolysis. J Therm Biol 1996; 21: 205–212
   Web of Science ®Google Scholar
• Ivanov IT, Todorova R, Zlatanov I. Spectrofluorometric and microcalorimetric study of the thermal poration relevant to the mechanism of thermohemolysis. Int J Hyperthermia 1999; 15: 29–43
   PubMed Web of Science ®Google Scholar
• Reithmeier RAF, Chan SL, Popov M. Structure of the erythrocyte band 3 anion exchanger. Handbook of Biological Physics Transport Processes in Eukaryotic and Prokaryotic Organisms, WN Konings, HR Kaback, JS Lolkema. Elsevier Science BV, AmsterdamThe Netherlands 1996; 2. 22: 281–309
   Google Scholar
• Casey JR, Reithmeier RA. Analysis of the oligomeric state of band 3, the anion transport protein of the human erythrocyte membrane, by size exclusion high performance liquid chromatography. Oligomeric stability and origin of heterogeneity. Biol Chem 1991; 266: 15726–15737
   Google Scholar
• Tanner MJ. Molecular and cellular biology of the erythrocyte anion exchanger (AE1). Semin Hematol 1993; 30: 34–57
   PubMed Web of Science ®Google Scholar
• Okubo K, Kang D, Hamasaki N, Jennings ML. Red blood cell band 3. Lysine 539 and lysine 851 react with the same DIDS (4,4′-diisothiocyanodihydrostilbene-2,2′-disulfonic acid) molecule. J Biol Chem 1994; 269: 1918–1926
   PubMed Web of Science ®Google Scholar
• Blackman SM, Piston DW, Beth AH. Oligomeric state of human erythrocyte band 3 measured by fluorescence resonance energy homotransfer. Biophys J 1998; 75: 1117–1130
   PubMed Web of Science ®Google Scholar
• Avigad LS, Bernheimer AW. Inhibition by zinc of hemolysis induced by bacterial and other cytolytic agents. Infect Immunity 1976; 13: 1378–1381
   PubMed Web of Science ®Google Scholar
• Ando K, Kikugawa K, Beppu M. Induction of band 3 aggregation in erythrocytes results in anti-band 3 autoantibody binding to the carbohydrate epitopes of band 3. Arch Biochem Biophys 1997; 339: 250–257
   PubMedGoogle Scholar
• Bosman GJ, Were JM, Willekens FL, Novotný VM. Erythrocyte ageing in vivo and in vitro: Structural aspects and implications for transfusion. Transfus Med 2008; 18: 335–347
   PubMed Web of Science ®Google Scholar
• Turrini F, Arese P, Yuan J, Low PS. Clustering of integral membrane proteins of the human erythrocyte membrane stimulates autologous IgG binding, complement deposition, and phagocytosis. J Biol Chem 1991; 266: 23611–23617
   PubMed Web of Science ®Google Scholar