Anion conductance of the human red cell is carried by a maxi-anion channel

Blood Cells, Molecules, and Diseases

Volumn 44, Issue 4, 2010, Pages 243-251

  Glogowska, Edyta ^a   Dyrda, Agnieszka ^a   Cueff, Anne ^a   Bouyer, Guillaume ^a   Egée, Stéphane ^a   Bennekou, Poul ^b   Thomas, Serge L Y ^a  

^a CNRS   (France)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Human red blood cell; Maxi anion channels; Membrane; Serum

Indexed keywords

ANION CHANNEL; CHLORIDE CHANNEL;

ANION TRANSPORT; ARTICLE; CELL ADHESION; CELL MEMBRANE DEPOLARIZATION; CELL MEMBRANE PERMEABILITY; CELL MEMBRANE POTENTIAL; CHANNEL GATING; CONTROLLED STUDY; ERYTHROCYTE; ERYTHROCYTE MEMBRANE; HUMAN; HUMAN CELL; PATCH CLAMP; PRIORITY JOURNAL;

ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; CHLORIDE CHANNELS; CHLORIDES; CULTURE MEDIA, SERUM-FREE; ERYTHROCYTES; HUMANS; ION CHANNEL GATING; NITROBENZOATES; PATCH-CLAMP TECHNIQUES; SERUM; THIOCYANATES; UP-REGULATION;

EID: 77950299991     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2010.02.014     Document Type: Article

References (58)

1. Tosteson D.C. Halide transport in red cells. Acta Physiol. Scand. 1959, 46:19-41.
2. Funder J., Wieth J.O. Chloride and hydrogen ion distribution between human red cells and plasma. Acta Physiol. Scand. 1966, 68:234-245.
3. Van Slyke D.D., Wu H., McLean F.C. Studies of gas and electrolyte equilibria in the blood. J. Biol. Chem. 1923, 56:765-849.
4. Warburg A. Studies on carbonic acid compounds and hydrogen ion activities in blood and salt solutions. Biochem. J. 1922, 16:153-340.
5. Manninen V. Movements of sodium and potassium ions and their tracers in propranolol-treated red cells and diaphragm muscle. Acta Physiol. Scand. 1970, 80:1-76.
6. Donlon J.A., Rothstein A. The cation permeability of erythrocytes in low ionic strength media of various tonicities. J. Membr. Biol. 1969, 1:37-52.
7. Johnson S.L., Woodbury J.W. Membrane resistance of human red cells. J. Gen. Physiol. 1964, 47:827-837.
8. Lassen U.V., Sten-Knudsen O. Direct measurement of membrane potential and membrane resistance of human red cells. J. Physiol. 1968, 195:681-696.
9. Hoffman J.F., Lassen U.V. Plasma membrane potentials in Amphiuma red cells. Abstract, XXV Int. Congr. Physiol. Sci., Munich 1971.
10. Lassen U.V. Membrane potential and membrane resistance of red cells. Alfred Benzon Symposium IV: oxygen affinity of hemoglobin and red cell acid-base status, Munksgaard, Copenhagen 1972, 291-306. M. Rorth, P. Astrup (Eds.).
11. Freedman J.C., Hoffman J.F. The relation between dicarbocyanine dye fluorescence and the membrane potential of human red blood cells set at varying Donnan equilibria. J. Gen. Physiol. 1979, 74:187-212.
12. Hoffman J.F., Laris P.C. Determination of membrane potentials in human and Amphiuma red blood cells by means of a fluorescent probe. J. Physiol. 1974, 239:519-552.
13. Chapell J.B., Crofts A.R. Ion transport and reversible volume changes of isolated mitochondria. Regulation of metabolic processes in mitochondria 1966, 293. Elsevier, Amsterdam. J.M. Tager, S. Papa, E. Quagliariello, E.C. Slater (Eds.).
14. Harris E.J., Pressman B.C. Obligate cation exchanges in red cells. Nature 1967, 216:918-920.
15. Pressman B.C., Heeb M.J. Effect of ionophorous antibiotics on the permeability of erythrocyte ghosts. Biophys. Soc. Abs 1971, 1971:310.
16. Scarpa A., Cecchetto A., Azzone G.F. Permeability of erythrocytes to anions and the regulation of cell volume. Nature 1968, 219:529-531.
17. Scarpa A., Cecchetto A., Azzone G.F. The mechanism of anion translocation and pH equilibration in erythrocytes. Biochim. Biophys. Acta 1970, 219:179-188.
18. Gunn R.B., Dalmark M., Tosteson D.C., Wieth J.O. Characteristics of chloride transport in human red blood cells. J. Gen. Physiol. 1973, 61:185-206.
19. Dalmark M., Wieth J.O. Temperature dependence of chloride, bromide, iodide, thiocyanate and salicylate transport in human red cells. J. Physiol. 1972, 224:583-610.
20. Lassen U.V., Pape L., Vestergaard-Bogind B. Chloride conductance of the Amphiuma red cell membrane. J. Membr. Biol. 1978, 39:27-48.
21. Hunter M.J. A quantitative estimate of the non-exchange-restricted chloride permeability of the human red cell. J. Physiol. 1971, 218:49P-50P.
22. Hunter M. Human erythrocyte anion permeabilities measured under conditions of net charge transfer. J. Physiol. 1977, 268:35-49.
23. Hoffman J.F., Kaplan J.H., Callahan T.J., Freedman J.C. Electrical resistance of the red cell membrane and the relation between net anion transport and the anion exchange mechanism. Ann. N. Y. Acad. Sci. 1980, 341:357-360.
24. Cabantchik Z.I., Rothstein A. The nature of the membrane sites controlling anion permeability of human red blood cells as determined by studies with disulfonic stilbene derivatives. J. Membr. Biol. 1972, 10:311-330.
25. Wolosin J.M., Ginsburg H., Cabantchick Z.I. Functional characterization of anion transport system isolated from human erythrocyte membranes. J. Biol. Chem. 1971, 252:2419-2427.
26. Knauf P., Fuhrmann G.F. Determination of chloride and sulphate conductance in human red blood cells. Fed. Proc. 1974, 33:1591.
27. Knauf P.A., Law F.Y., Marchant P.J. Relationship of net chloride flow across the human erythrocyte membrane to the anion exchange mechanism. J. Gen. Physiol. 1983, 81:95-126.
28. Bennekou P., Stampe P. The effect of ATP, intracellular calcium and the anion exchange inhibitor DIDS on conductive anion fluxes across the human red cell membrane. Biochim. Biophys. Acta 1988, 942:179-185.
29. Gasbjerg P.K., Funder J., Brahm J. Kinetics of residual chloride transport in human red blood cells after maximum covalent 4, 4′-diisothiocyanostilbene-2, 2′-disulfonic acid binding. J. Gen. Physiol. 1993, 101:715-732.
30. Kaplan J.H., Pring M., Passow H. Band-3 protein-mediated anion conductance of the red cell membrane. Slippage vs ionic diffusion. FEBS Lett. 1983, 156:175-179.
31. Vestergaard-Bogind B. and U.V. Lassen. Comparative biochemistry and physiology of transport 1974, 346-353. Elsevier, New-york. L. Bolis, K. Bloch, S.E. Luria, F. Lynen (Eds.).
32. Frölich O. Chloride net transport of the human erythrocyte at low extracellular chloride concentrations. Biophys. J. 1981, 33:2a.
33. Alper S.L., Darman R.B., Chernova M.N., Dahl N.K. The AE gene family of Cl/HCO3- exchangers. J. Nephrol. 2002, 15(Suppl 5):S41-S53.
34. Schwarz W., Gryorczyk R., Hof D. Recording single-channel currents from human red cells. Methods Enzymol. 1989, 173:112-121.
35. Desai S.A., Bezrukov S.M., Zimmerberg J. A voltage-dependent channel involved in nutrient uptake by red blood cells infected with the malaria parasite. Nature 2000, 406:1001-1005.
36. Egee S., Lapaix F., Decherf G., Staines H.M., et al. A stretch-activated anion channel is up-regulated by the malaria parasite Plasmodium falciparum. J. Physiol. 2002, 542:795-801.
37. Bouyer G., Egee S., Thomas S.L. Three types of spontaneously active anionic channels in malaria-infected human red blood cells. Blood Cells Mol. Dis. 2006, 36:248-254.
38. Bouyer G., Egee S., Thomas S.L. Toward a unifying model of malaria-induced channel activity. Proc. Natl. Acad. Sci. U. S. A. 2007, 104:11044-11049.
39. Decherf G., Bouyer G., Egee S., Thomas S.L. Chloride channels in normal and cystic fibrosis human erythrocyte membrane. Blood Cells Mol. Dis. 2007, 39:24-34.
40. Decherf G., Egee S., Staines H.M., Ellory J.C., et al. Anionic channels in malaria-infected human red blood cells. Blood Cells Mol. Dis. 2004, 32:366-371.
41. Verloo P., Kocken C.H., Van Der Wel A., Tilly B.C., et al. Plasmodium falciparum-activated chloride channels are defective in erythrocytes from cystic fibrosis patients. J. Biol. Chem. 2004, 279:103216-110322.
42. + channels and muscarinic and purinergic receptors identified in human erythroid progenitor cells and red blood cell ghosts. Proc. Natl. Acad. Sci. U. S. A. 2004, 101:12370-12374.
43. Schwiebert E.M., Flotte T., Cutting G.R., Guggino W.B. Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents. Am. J. Physiol. 1994, 266:C1464-C1477.
44. Schwiebert E.M., Gruenert D.C., Guggino W.B., Stanton B.A. G protein G alpha i-2 inhibits outwardly rectifying chloride channels in human airway epithelial cells. Am. J. Physiol. 1995, 269:C451-C456.
45. Tabcharani J.A., Hanrahan J.W. On the activation of outwardly rectifying anion channels in excised patches. Am. J. Physiol. 1991, 261:G992-G999.
46. Duranton C., Huber S.M., Lang F. Oxidation induces a Cl(-)-dependent cation conductance in human red blood cells. J. Physiol. 2002, 539:847-855.
47. Huber S.M., Duranton C., Henke G., Van De Sand C., et al. Plasmodium induces swelling-activated ClC-2 anion channels in the host erythrocyte. J. Biol. Chem. 2004, 279:41444-41452.
48. Staines H.M., Powell T., Ellory J.C., Egee S., et al. Modulation of whole-cell currents in Plasmodium falciparum-infected human red blood cells by holding potential and serum. J. Physiol. 2003, 552:177-183.
49. Duranton C., Tanneur V., Lang C., Brand V.B., et al. A high specificity and affinity interaction with serum albumin stimulates an anion conductance in malaria-infected erythrocytes. Cell. Physiol. Biochem. 2008, 22:395-404.
50. Parker J.C. Hemolytic action of potassium salts on dog red blood cells. Am. J. Physiol. 1983, 244:C313-C317.
51. Tiffert T., Daw N., Perdomo D., Lew V.L. A fast and simple screening test to search for specific inhibitors of the plasma membrane calcium pump. J. Lab. Clin. Med. 2001, 137:199-207.
52. Bathori G., Szabo I., Schmehl I., Tombola F., et al. Novel aspects of the electrophysiology of mitochondrial porin. Biochem. Biophys. Res. Commun. 1998, 243:258-263.
53. Decherf G., Egee S., Lapaix F., Staines H., et al. Chloride channels in human red blood cell membrane, 14th Meeting of the European Association for Red Cell Research, Roscoff, France 2003.
54. Payne J.A., Lytle C., McManus T.J. Foreign anion substitution for chloride in human red blood cells: effect on ionic and osmotic equilibria. Am. J. Physiol. 1990, 259:C819-C827.
55. Kakhniashvili D.G., Bulla L.A., Goodman S.R. The human erythrocyte proteome. Mol. Cell. Proteomics 2004, 3:501-509.
56. Veenman L., Papadopoulos V., Gavish M. Channel-like functions of the 18-kDa translocator protein (TSPO): regulation of apoptosis and steroidogenesis as part of the host-defense response. Curr. Pharm. Des. 2007, 13:2385-2405.
57. Olson J.M., Ciliax B.J., Mancini W.R., Young A.B. Presence of peripheral-type benzodiazepine binding sites on human erythrocyte membranes. Eur. J. Pharmacol. 1988, 152:47-53.
58. Canat X., Carayon P., Bouaboula M., Cahard D., et al. Distribution profile and properties of peripheral-type benzodiazepine receptors on human hemopoietic cells. Life Sci. 1993, 52:107-118.