The plasmodial surface anion channel is functionally conserved in divergent malaria parasites

Eukaryotic Cell

Volumn 4, Issue 12, 2005, Pages 2153-2159

  Lisk, Godfrey ^a   Desai, Sanjay A ^a  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANION; ION CHANNEL; TRITIUM;

ANIMAL; ARTICLE; CELL MEMBRANE PERMEABILITY; CELL MEMBRANE POTENTIAL; CHANNEL GATING; CHEMISTRY; COMPARATIVE STUDY; DRUG EFFECT; ELECTROPHYSIOLOGY; ERYTHROCYTE; ERYTHROCYTE MEMBRANE; GENETICS; HUMAN; KINETICS; MACACA; MALARIA; MALARIA FALCIPARUM; METABOLISM; OSMOTIC FRAGILITY; PARASITOLOGY; PATCH CLAMP; PHYSIOLOGY; PLASMODIUM FALCIPARUM; PLASMODIUM KNOWLESI;

ANIMALS; ANIONS; CELL MEMBRANE PERMEABILITY; ELECTROPHYSIOLOGY; ERYTHROCYTE MEMBRANE; ERYTHROCYTES; HUMANS; ION CHANNEL GATING; ION CHANNELS; KINETICS; MACACA MULATTA; MALARIA; MALARIA, FALCIPARUM; MEMBRANE POTENTIALS; OSMOTIC FRAGILITY; PATCH-CLAMP TECHNIQUES; PLASMODIUM FALCIPARUM; PLASMODIUM KNOWLESI; TRITIUM;

MACACA MULATTA; PLASMODIUM FALCIPARUM; PLASMODIUM KNOWLESI;

EID: 29144503753     PISSN: 15359778     EISSN: None     Source Type: Journal    
DOI: 10.1128/EC.4.12.2153-2159.2005     Document Type: Article

References (40)

1. Aley, S. B., J. A. Sherwood, and R. J. Howard. 1984. Knob-positive and knob-negative Plasmodium falciparum differ in expression of a strain-specific malarial antigen on the surface of infected erythrocytes. J. Exp. Med. 160:1585-1590.
2. Alkhalil, A., J. V. Cohn, M. A. Wagner, J. S. Cabrera, T. Rajapandi, and S. A. Desai. 2004. Plasmodium falciparum likely encodes the principal anion channel on infected human erythrocytes. Blood 104:4279-4286.
3. Ancelin, M. L., M. Parant, M. J. Thuet, J. R. Philippot, and H. J. Vial. 1991. Increased permeability to choline in simian erythrocytes after Plasmodium knowlesi infection. Biochem. J. 273:701-709.
4. Biagini, G. A., E. M. Pasini, R. Hughes, H. P. De Koning, H. J. Vial, P. M. O'Neill, S. A. Ward, and P. G. Bray. 2004. Characterization of the choline carrier of Plasmodium falciparum: a route for the selective delivery of novel antimalarial drugs. Blood 104:3372-3377.
5. + exclusion. Mol. Biochem. Parasitol. 132:27-34.
6. Desai, S. A. 2005. Open and closed states of the plasmodial surface anion channel. Nanomed. Nanotechnol. Biol. Med. 1:58-66.
7. Desai, S. A., A. Alkhalil, M. Kang, U. Ashfaq, and M. L. Nguyen. 2005. PSAC-independent phloridzin resistance in Plasmodium falciparum. J. Biol. Chem. 280:16861-16867.
8. Desai, S. A., S. M. Bezrukov, and J. Zimmerberg. 2000. A voltage-dependent channel involved in nutrient uptake by red blood cells infected with the malaria parasite. Nature 406:1001-1005.
9. Desai, S. A., D. J. Krogstad, and E. W. McCleskey. 1993. A nutrient-permeable channel on the intraerythrocytic malaria parasite. Nature 362:643-646.
10. Desai, S. A., and R. L. Rosenberg. 1997. Pore size of the malaria parasite's nutrient channel. Proc. Natl. Acad. Sci. USA 94:2045-2049.
11. 2+ entry matches active extrusion in human erythrocytes. J. Gen. Physiol. 98:349-364.
12. Egee, S., F. Lapaix, G. Decherf, H. M. Staines, J. C. Ellory, C. Doerig, and S. L. Thomas. 2002. A stretch-activated anion channel is up-regulated by the malaria parasite Plasmodium falciparum. J. Physiol. 542:795-801.
13. Elliott, J. L., K. J. Saliba, and K. Kirk. 2001. Transport of lactate and pyruvate in the intraerythrocytic malaria parasite, Plasmodium falciparum. Biochem. J. 355:733-739.
14. Escalante, A. A., and F. J. Ayala. 1994. Phylogeny of the malarial genus Plasmodium, derived from rRNA gene sequences. Proc. Natl. Acad. Sci. USA 91:11373-11377.
15. Escalante, A. A., O. E. Cornejo, D. E. Freeland, A. C. Poe, E. Durrego, W. E. Collins, and A. A. Lal. 2005. A monkey's tale: the origin of Plasmodium vivax as a human malaria parasite. Proc. Natl. Acad. Sci. USA 102:1980-1985.
16. Gati, W. P., A. N. Lin, T. I. Wang, J. D. Young, and A. R. Paterson. 1990. Parasite-induced processes for adenosine permeation in mouse erythrocytes infected with the malarial parasite Plasmodium yoelii. Biochem. J. 272:277-280.
17. Ginsburg, H., S. Kutner, M. Krugliak, and Z. I. Cabantchik. 1985. Characterization of permeation pathways appearing in the host membrane of Plasmodium falciparum infected red blood cells. Mol. Biochem. Parasitol. 14:313-322.
18. Goldman, D. E. 1943. Potential, impedance, and rectification in membranes. J. Gen. Physiol. 27:37-60.
19. Homewood, C. A., and K. D. Neame. 1974. Malaria and the permeability of the host erythrocyte. Nature 252:718-719.
20. Huber, S. M., C. Duranton, G. Henke, C. Van De Sand, V. Heussler, E. Shumilina, C. D. Sandu, V. Tanneur, V. Brand, R. S. Kasinathan, K. S. Lang, P. G. Kremsner, C. A. Hubner, M. B. Rust, K. Dedek, T. J. Jentsch, and F. Lang. 2004. Plasmodium induces swelling-activated ClC-2 anion channels in the host erythrocyte. J. Biol. Chem. 279:41444-41452.
21. - channels of human erythrocytes by membrane oxidation. EMBO J. 21:22-30.
22. Kang, M., G. Lisk, S. Hollingworth, S. M. Baylor, and S. A. Desai. 2005. Malaria parasites are rapidly killed by dantrolene derivatives specific for the plasmodial surface anion channel. Mol. Pharmacol. 68:34-40.
23. Kirk, K., H. A. Horner, B. C. Elford, J. C. Ellory, and C. I. Newbold. 1994. Transport of diverse substrates into malaria-infected erythrocytes via a pathway showing functional characteristics of a chloride channel. J. Biol. Chem. 269:3339-3347.
24. Kirk, K., H. A. Horner, D. J. Spillett, and B. C. Elford. 1993. Glibenclamide and meglitinide block the transport of low molecular weight solutes into malaria-infected erythrocytes. FEBS Lett. 323:123-128.
25. Kutner, S., W. V. Breuer, H. Ginsburg, and Z. I. Cabantchik. 1987. On the mode of action of phlorizin as an antimalarial agent in in vitro cultures of Plasmodium falciparum. Biochem. Pharmacol. 36:123-129.
26. Myint, O., W. J. O'Sullivan, and A. M. Gero. 1997, Laboratory and field comparisons of adenosine influx in Plasmodium falciparum and Plasmodium vivax infected erythrocytes with genetic abnormalities from patients in Myanmar. Southeast Asian J. Trop. Med. Public Health 28:22-31.
27. Overman, R. R. 1948. Reversible cellular permeability alterations in disease. In vivo studies on sodium, potassium and chloride concentrations in erythrocytes of the malarious monkey. Am. J. Physiol. 152:113-121.
28. Page, S. L., C. Chiu, and M. Goodman. 1999. Molecular phylogeny of Old World monkeys (Cercopithecidae) as inferred from gamma-globin DNA sequences. Mol. Phylogenet. Evol. 13:348-359.
29. Rager, N., C. B. Mamoun, N. S. Carter, D. E. Goldberg, and B. Ullman. 2001. Localization of the Plasmodium falciparum PfNT1 nucleoside transporter to the parasite plasma membrane. J. Biol. Chem. 276:41095-41099.
30. Rathore, D., A. M. Wahl, M. Sullivan, and T. F. McCutchan. 2001. A phylogenetic comparison of gene trees constructed from plastid, mitochondrial and genomic DNA of Plasmodium species. Mol. Biochem. Parasitol. 114:89-94.
31. Rich, S. M., M. C. Licht, R. R. Hudson, and F. J. Ayala. 1998. Malaria's Eve: evidence of a recent population bottleneck throughout the world populations of Plasmodium falciparum. Proc. Natl. Acad. Sci. USA 95:4425-4430.
32. Staines, H. M., E. M. Godfrey, F. Lapaix, S. Egee, S. Thomas, and J. C. Ellory. 2002. Two functionally distinct organic osmolyte pathways in Plasmodium gaffinaceum-infected chicken red blood cells. Biochim. Biophys. Acta 1561:98-108.
33. Staines, H. M., and K. Kirk. 1998. Increased choline transport in erythrocytes from mice infected with the malaria parasite Plasmodium vinckei vinckei. Biochem. J. 334:525-530.
34. Staines, H. M., T. Powell, J. C. Ellory, S. Egee, F. Lapaix, G. Decherf, S. L. Thomas, C. Duranton, F. Lang, and S. M. Huber. 2003. Modulation of whole-cell currents in Plasmodium falciparum-infected human red blood cells by holding potential and serum. J. Physiol. 552:177-183.
35. Thierry, B., E. Andre, and P. Imbs. 2000. Hematologic and plasma biochemical values for Tonkean macaques (Macaca tonkeana). J. Zoo Wildl. Med. 31:179-184.
36. Thomas, S. L., S. Egee, F. Lapaix, L. Kaestner, H. M. Staines, and J. C. Ellory. 2001, Malaria parasite Plasmodium gallinaceum up-regulates host red blood cell channels. FEBS Lett. 500:45-51.
37. Verloo, P., C. H. Kocken, A. van der Wel, B. C. Tilly, B. M. Hogema, M. Sinaasappel, A. W. Thomas, and H. R. De Jonge. 2004. Plasmodium falciparum-activated chloride channels are defective in erythrocytes from cystic fibrosis patients. J. Biol. Chem. 279:10316-10322.
38. Wagner, M. A., B. Andemariam, and S. A. Desai. 2003. A two-compartment model of osmotic lysis in Plasmodium falciparum-infected erythrocytes. Biophys. J. 84:116-123.
39. Woodrow, C. J., J. I. Penny, and S. Krishna. 1999. Intraerythrocytic Plasmodium falciparum expresses a high affinity facilitative hexose transporter. J. Biol. Chem. 274:7272-7277.
40. Wright, E. M., and J. M. Diamond. 1977. Anion selectivity in biological systems. Physiol. Rev. 57:109-156.