Intracellular localization of ClC chloride channels and their ability to form hetero-oligomers

Journal of Cellular Physiology

Volumn 206, Issue 3, 2006, Pages 792-798

  Suzuki, Tatsunori ^a   Rai, Tatemitsu ^a   Hayama, Atsushi ^a   Sohara, Eisei ^a   Suda, Shin ^a   Itoh, Tomohiro ^a   Sasaki, Sei ^a   Uchida, Shinichi ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL; CLC CHLORIDE CHANNEL; OLIGOMER; PROTEIN; PROTEIN CLC 3; PROTEIN CLC 4; PROTEIN CLC 5; PROTEIN CLC 6; PROTEIN CLC 7; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CELL MEMBRANE; CELL ORGANELLE; CELL STRAIN HEK293; CELL TYPE; CONTROLLED STUDY; EMBRYO; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE TEST; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; RAT; STATISTICAL SIGNIFICANCE;

BIOLOGICAL MARKERS; CELL LINE; CELL MEMBRANE; CHLORIDE CHANNELS; ENDOSOMES; EPITOPES; FLUORESCENT ANTIBODY TECHNIQUE; HUMANS; IMMUNOPRECIPITATION; MODELS, BIOLOGICAL; ORGANELLES; PEPTIDES; TRANSFECTION;

ANIMALIA;

EID: 31944449588     PISSN: 00219541     EISSN: None     Source Type: Journal    
DOI: 10.1002/jcp.20516     Document Type: Article

References (32)

1. Brandt S, Jentsch TJ. 1995. ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family. FEBS Lett 377(1):15-20.
2. Britton FC, Hatton WJ, Rossow CF, Duan D, Hume JR, Horowitz B. 2000. Molecular distribution of volume-regulated chloride channels (ClC-2 and ClC-3) in cardiac tissues. Am J Physiol Heart Circ Physiol 279(5):H2225-H2233.
3. Dutzler R, Campbell EB, Cadene M, Chait BT, MacKinnon R. 2002. X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity. Nature 415(6869):287-294.
4. Fisher SE, Black GC, Lloyd SE, Hatchwell E, Wrong O, Thakker RV, Craig IW. 1994. Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). Hum Mol Genet 3(11):2053-2059.
5. Friedrich T, Breiderhoff T, Jentsch TJ. 1999. Mutational analysis demonstrates that ClC-4 and ClC-5 directly mediate plasma membrane currents. J Biol Chem 274(2):896-902.
6. Gentzsch M, Cui L, Mengos A, Chang XB, Chen JH, Riordan JR. 2003. The PDZ-binding chloride channel ClC-3B localizes to the Golgi and associates with cystic fibrosis transmembrane conductance regulator-interacting PDZ proteins. J Biol Chem 278(8):6440-6449.
7. Gong W, Xu H, Shimizu T, Morishima S, Tanabe S, Tachibe T, Uchida S, Sasaki S, Okada Y. 2004. ClC-3-independent, PKC-dependent activity of volume-sensitive Cl channel in mouse ventricular cardiomyocytes. Cell Physiol Biochem 14(4-6):213-224.
8. Gunther W, Luchow A, Cluzeaud F, Vandewalle A, Jentsch TJ. 1998. ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells. Proc Natl Acad Sci USA 95(14):8075-8080.
9. Hara-Chikuma M, Yang B, Sonawane ND, Sasaki S, Uchida S, Verkman AS. 2004. ClC-3 chloride channels facilitate endosomal acidification and chloride accumulation. J Biol Chem 280(2):1241-1247.
10. 2+/ calmodulin-dependent protein kinase. J Biol Chem 276(23):20093-20100.
11. Jentsch TJ, Gunther W, Pusch M, Schwappach B. 1995. Properties of voltage-gated chloride channels of the ClC gene family. J Physiol 482:19S-25S.
12. Jentsch TJ, Stein V, Weinreich F, Zdebik AA. 2002. Molecular structure and physiological function of chloride channels. Physiol Rev 82(2):503-568.
13. Kawasaki M, Uchida S, Monkawa T, Miyawaki A, Mikoshiba K, Marumo F, Sasaki S. 1994. Cloning and expression of a protein kinase C-regulated chloride channel abundantly expressed in rat brain neuronal cells. Neuron 12(3):597-604.
14. Kida Y, Uchida S, Miyazaki H, Sasaki S, Marumo F. 2001. Localization of mouse CLC-6 and CLC-7 mRNA and their functional complementation of yeast CLC gene mutant. Histochem Cell Biol 115(3):189-194.
15. Kornak U, Kasper D, Bosl MR, Kaiser E, Schweizer M, Schulz A, Friedrich W, Delling G, Jentsch TJ. 2001. Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man. Cell 104(2):205-215.
16. Li X, Wang T, Zhao Z, Weinman SA. 2002. The ClC-3 chloride channel promotes acidification of lysosomes in CHO-K1 and Huh-7 cells. Am J Physiol Cell Physiol 282(6):C1483-C1491.
17. Lloyd SE, Pearce SH, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SP, Wrong O, Jentsch TJ, Craig IW, Thakker RV. 1996. A common molecular basis for three inherited kidney stone diseases. Nature 379(6564):445-449.
18. Ludewig U, Pusch M, Jentsch TJ. 1996. Two physically distinct pores in the dimeric ClC-0 chloride channel. Nature 383(6598):340-343.
19. Middleton RE, Pheasant DJ, Miller C. 1996. Homodimeric architecture of a ClC-type chloride ion channel. Nature 383(6598):337-340.
20. Mindell JA, Maduke M, Miller C, Grigorieff N. 2001. Projection structure of a ClC-type chloride channel at 6.5 A resolution. Nature 409(6817):219-223.
21. Mohammad-Panah R, Ackerley C, Rommens J, Choudhury M, Wang Y, Bear CE. 2002. The chloride channel ClC-4 co-localizes with cystic fibrosis transmembrane conductance regulator and may mediate chloride flux across the apical membrane of intestinal epithelia. J Biol Chem 277(1):566-574.
22. Mohammad-Panah R, Harrison R, Dhani S, Ackerley C, Huan LJ, Wang Y, Bear CE. 2003. The chloride channel ClC-4 contributes to endosomal acidification and trafficking. J Biol Chem 278(31):29267-29277.
23. Obermuller N, Gretz N, Kriz W, Reilly RF, Witzgall R. 1998. The swelling-activated chloride channel ClC-2, the chloride channel ClC-3, and ClC-5, a chloride channel mutated in kidney stone disease, are expressed in distinct subpopulations of renal epithelial cells. J Clin Invest 101(3):635-642.
24. - channel disruption impairs endocytosis in a mouse model for Dent's disease. Nature 408(6810):369-373.
25. - channels. J Biol Chem 271(17):10210-10216.
26. Salazar G, Love R, Styers ML, Werner E, Peden A, Rodriguez S, Gearing M, Wainer BH, Faundez V. 2004. AP-3-dependent mechanisms control the targeting of a chloride channel (ClC-3) in neuronal and non-neuronal cells. J Biol Chem 279(24):25430-25439.
27. Shimada K, Li X, Xu G, Nowak DE, Showalter LA, Weinman SA. 2000. Expression and canalicular localization of two isoforms of the ClC-3 chloride channel from rat hepatocytes. Am J Physiol Gastrointest Liver Physiol 279(2):G268-G276.
28. Steinmeyer K, Lorenz C, Pusch M, Koch MC, Jentsch TJ. 1994. Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen). Embo J 13(4):737-743.
29. Stobrawa SM, Breiderhoff T, Takamori S, Engel D, Schweizer M, Zdebik AA, Bosl MR, Ruether K, Jahn H, Draguhn A, Jahn R, Jentsch TJ. 2001. Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus. Neuron 29(1):185-196.
30. van Slegtenhorst MA, Bassi MT, Borsani G, Wapenaar MC, Ferrero GB, de Conciliis L, Rugarli EI, Grillo A, Franco B, Zoghbi HY, et al. 1994. A gene from the Xp22.3 region shares homology with voltage-gated chloride channels. Hum Mol Genet 3(4):547-552.
31. Weinreich F, Jentsch TJ. 2001. Pores formed by single subunits in mixed dimers of different CLC chloride channels. J Biol Chem 276(4):2347-2353.
32. Yoshikawa M, Uchida S, Ezaki J, Rai T, Hayama A, Kobayashi K, Kida Y, Noda M, Koike M, Uchiyama Y, Marumo F, Kominami E, Sasaki S. 2002. CLC-3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis. Genes Cells 7(6):597-605.