Characterization of ion channel and transporter mRNA expressions in isolated gill chloride and pavement cells of seawater acclimating eels

Biochemical and Biophysical Research Communications

Volumn 346, Issue 4, 2006, Pages 1181-1190

  Tse, William K F ^a   Au, Doris W T ^b   Wong, Chris K C ^a  

^a HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

^b CITY UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); AQUAPORIN 3; CHLORIDE; ION CHANNEL; MESSENGER RNA; SEA WATER; SODIUM PROTON EXCHANGE PROTEIN 1;

ACCLIMATIZATION; ANIMAL CELL; ARTICLE; CELL COUNT; CELL SIZE; CHLORIDE TRANSPORT; CONTROLLED STUDY; EEL; GENE EXPRESSION; GILL; IMMUNOCYTOCHEMISTRY; IMMUNOREACTIVITY; NONHUMAN; NUCLEOTIDE SEQUENCE; POTASSIUM TRANSPORT; PRIORITY JOURNAL; PROTEIN EXPRESSION; SODIUM TRANSPORT; STAINING; STATISTICAL SIGNIFICANCE; UPREGULATION;

ACCLIMATIZATION; ANIMALS; BLOTTING, WESTERN; CELLS, CULTURED; CHLORIDES; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EELS; GILLS; IMMUNOHISTOCHEMISTRY; NA(+)-K(+)-EXCHANGING ATPASE; POTASSIUM CHANNELS, INWARDLY RECTIFYING; SEAWATER; SODIUM-POTASSIUM-CHLORIDE SYMPORTERS;

ANGUILLA JAPONICA; TELEOSTEI;

EID: 33745381216     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.06.028     Document Type: Article

References (29)

1. Evans D.H., Piermarini P.M., and Choe K.P. The multifunctional fish gill: dominant site of gas exchange, osmoregulation, acid-base regulation, and excretion of nitrogenous waste. Physiol. Rev. 85 (2005) 97-177
2. Hirose S., Kaneko T., Naito N., and Takei Y. Molecular biology of major components of chloride cells. Comp. Biochem. Physiol. B. Biochem. Mol. Biol. 136 (2003) 593-620
3. Perry S.F. The chloride cell: structure and function in the gills of freshwater fishes. Annu. Rev. Physiol. 59 (1997) 325-347
4. Pisam M., Sardet C., and Maetz J. Polysaccharidic material in chloride cell of teleostean gill: modifications according to salinity. Am. J. Physiol. 238 (1980) R213-R218
5. Pisam M. Membranous systems in the "chloride cell" of teleostean fish gill; their modifications in response to the salinity of the environment. Anat. Rec. 200 (1981) 401-414
6. Pisam M., Prunet P., Boeuf G., and Rambourg A. Ultrastructural features of chloride cells in the gill epithelium of the Atlantic salmon, Salmo salar, and their modifications during smoltification. Am. J. Anat. 183 (1988) 235-244
7. Pisam M., Boeuf G., Prunet P., and Rambourg A. Ultrastructural features of mitochondria-rich cells in stenohaline freshwater and seawater fishes. Am. J. Anat. 187 (1990) 21-31
8. Shirai N., and Utida S. Development and degeneration of the chloride cell during seawater and freshwater adaptation of the japanese eel, Anguilla japonica. Z. Zellforsch. Mikrosk. Anat. 103 (1970) 247-264
9. Scott G.R., Richards J.G., Forbush B., Isenring P., and Schulte P.M. Changes in gene expression in gills of the euryhaline killifish Fundulus heteroclitus after abrupt salinity transfer. Am. J. Physiol. Cell Physiol. 287 (2004) C300-C309
10. Cutler C.P., and Cramb G. Branchial expression of an aquaporin 3 (AQP-3) homologue is downregulated in the European eel Anguilla anguilla following seawater acclimation. J. Exp. Biol. 205 (2002) 2643-2651
11. Katoh F., and Kaneko T. Short-term transformation and long-term replacement of branchial chloride cells in killifish transferred from seawater to freshwater, revealed by morphofunctional observations and a newly established 'time-differential double fluorescent staining' technique. J. Exp. Biol. 206 (2003) 4113-4123
12. Katoh F., Hyodo S., and Kaneko T. Vacuolar-type proton pump in the basolateral plasma membrane energizes ion uptake in branchial mitochondria-rich cells of killifish Fundulus heteroclitus, adapted to a low ion environment. J. Exp. Biol. 206 (2003) 793-803
13. Lignot J.H., Cutler C.P., Hazon N., and Cramb G. Immunolocalisation of aquaporin 3 in the gill and the gastrointestinal tract of the European eel Anguilla anguilla (L.). J. Exp. Biol. 205 (2002) 2653-2663
14. Marshall W.S., Lynch E.M., and Cozzi R.R. Redistribution of immunofluorescence of CFTR anion channel and NKCC cotransporter in chloride cells during adaptation of the killifish Fundulus heteroclitus to sea water. J. Exp. Biol. 205 (2002) 1265-1273
15. McCormick S.D., Sundell K., Bjornsson B.T., Brown C.L., and Hiroi J. Influence of salinity on the localization of Na+/K+-ATPase, Na+/K+/2Cl- cotransporter (NKCC) and CFTR anion channel in chloride cells of the Hawaiian goby (Stenogobius hawaiiensis). J. Exp. Biol. 206 (2003) 4575-4583
16. Suzuki Y., Itakura M., Kashiwagi M., Nakamura N., Matsuki T., Sakuta H., Naito N., Takano K., Fujita T., and Hirose S. Identification by differential display of a hypertonicity-inducible inward rectifier potassium channel highly expressed in chloride cells. J. Biol. Chem. 274 (1999) 11376-11382
17. Watanabe S., Kaneko T., and Aida K. Aquaporin-3 expressed in the basolateral membrane of gill chloride cells in Mozambique tilapia Oreochromis mossambicus adapted to freshwater and seawater. J. Exp. Biol. 208 (2005) 2673-2682
18. Wilson J.M., Laurent P., Tufts B.L., Benos D.J., Donowitz M., Vogl A.W., and Randall D.J. NaCl uptake by the branchial epithelium in freshwater teleost fish: an immunological approach to ion-transport protein localization. J. Exp. Biol. 203 Pt 15 (2000) 2279-2296
19. Kelly S.P., and Wood C.M. Effect of cortisol on the physiology of cultured pavement cell epithelia from freshwater trout gills. Am. J. Physiol. Regul. Integr. Comp. Physiol. 281 (2001) R811-R820
20. Zhou B., Kelly S.P., Ianowski J.P., and Wood C.M. Effects of cortisol and prolactin on Na+ and Cl- transport in cultured branchial epithelia from FW rainbow trout. Am. J. Physiol. Regul. Integr. Comp. Physiol. 285 (2003) R1305-R1316
21. Wong C.K., and Chan D.K. Chloride cell subtypes in the gill epithelium of Japanese eel Anguilla japonica. Am. J. Physiol. 277 (1999) R517-R522
22. Wong C.K., and Chan D.K. Isolation of viable cell types from the gill epithelium of Japanese eel Anguilla japonica. Am. J. Physiol. 276 (1999) R363-R372
23. Wong C.K., and Chan D.K. Effects of cortisol on chloride cells in the gill epithelium of Japanese eel, Anguilla japonica. J. Endocrinol. 168 (2001) 185-192
24. Goss G.G., Adamia S., and Galvez F. Peanut lectin binds to a subpopulation of mitochondria-rich cells in the rainbow trout gill epithelium. Am. J. Physiol. Regul. Integr. Comp. Physiol. 281 (2001) R1718-R1725
25. Reid S.D., Hawkings G.S., Galvez F., and Goss G.G. Localization and characterization of phenamil-sensitive Na+ influx in isolated rainbow trout gill epithelial cells. J. Exp. Biol. 206 (2003) 551-559
26. Galvez F., Reid S.D., Hawkings G., and Goss G.G. Isolation and characterization of mitochondria-rich cell types from the gill of freshwater rainbow trout. Am. J. Physiol. Regul. Integr. Comp. Physiol. 282 (2002) R658-R668
27. Van Lieburg A.F., Knoers N.V., and Deen P.M. Discovery of aquaporins: a breakthrough in research on renal water transport. Pediatr. Nephrol. 9 (1995) 228-234
28. Claiborne J.B., Blackston C.R., Choe K.P., Dawson D.C., Harris S.P., Mackenzie L.A., and Morrison-Shetlar A.I. A mechanism for branchial acid excretion in marine fish: identification of multiple Na+/H+ antiporter (NHE) isoforms in gills of two seawater teleosts. J. Exp. Biol. 202 (1999) 315-324
29. Key A.B., and Willmer E.N. Chloride-secreting cells in the gills of fishes, with special reference to the common eel. J. Physiol. (Lond.) 76 (1932) 368-378