Chloride transport in NCL-SG3 sweat gland cells: Channels involved

Experimental and Molecular Pathology

Volumn 83, Issue 1, 2007, Pages 47-53

  Servetnyk, Z ^a   Roomans, G M ^a  

^a UPPSALA UNIVERSITY   (Sweden)

Author keywords

Ca2+ activated chloride channel; Chloride transport; Cystic fibrosis transmembrane conductance regulator; Sweat gland

Indexed keywords

4,4' DIISOTHIOCYANATODIHYDROSTILBENE 2,2' DISULFONIC ACID; ADENOSINE TRIPHOSPHATE; CALCIUM ACTIVATED CHLORIDE CHANNEL; CALCIUM IONOPHORE; CHLORIDE; CHLORIDE CHANNEL; FORSKOLIN; GADOLINIUM; ISOBUTYLMETHYLXANTHINE; NIFLUMIC ACID; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; URIDINE TRIPHOSPHATE;

ARTICLE; CELL CULTURE; CELL IMMORTALIZATION; CELL INTERACTION; CHLORIDE TRANSPORT; CONTROLLED STUDY; EFFUSION; FLOW CYTOMETRY; FLUORESCENCE; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; IN VITRO STUDY; PROTEIN EXPRESSION; SWEAT GLAND;

BIOLOGICAL MARKERS; CALCIUM; CELL LINE; CHLORIDE CHANNELS; CHLORIDES; EPITHELIAL CELLS; HUMANS; IMMUNOHISTOCHEMISTRY; ION CHANNEL GATING; ION TRANSPORT; MICROSCOPY, ELECTRON, TRANSMISSION; SWEAT GLANDS;

EID: 34249804786     PISSN: 00144800     EISSN: 10960945     Source Type: Journal    
DOI: 10.1016/j.yexmp.2007.02.003     Document Type: Article

References (42)

1. Anderson M.P., Rich D.P., et al. Generation of cAMP-activated chloride currents by expression of CFTR. Science 251 4994 (1991) 679-682
2. Anderson M.P., Sheppard D.N., et al. Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia. Am. J. Physiol. 263 1 Pt 1 (1992) L1-L14
3. Bell C.L., Reddy M.M., et al. Reversed anion selectivity in cultured cystic fibrosis sweat duct cells. Am. J. Physiol. 262 1 Pt 1 (1992) C32-C38
4. Buchanan J.A., Yeger H., et al. Transformed sweat gland and nasal epithelial cell lines from control and cystic fibrosis individuals. J. Cell Sci. 95 Pt 1 (1990) 109-123
5. Chu C.S., Trapnell B.C., et al. Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium. Embo J. 10 6 (1991) 1355-1363
6. Cohn J.A., Melhus O., et al. CFTR: development of high-affinity antibodies and localization in sweat gland. Biochem Biophys Res. Commun. 181 1 (1991) 36-43
7. Eggermont J. Calcium-activated chloride channels: (un)known, (un)loved?. Proc. Am. Thorac. Soc. 1 1 (2004) 22-27
8. - current activated by cell swelling in rabbit portal vein vascular smooth muscle cells. Am. J. Physiol. 275 5 Pt 2 (1998) H1524-H1532
9. Jackson P.S., Morrison R., et al. The volume-sensitive organic osmolyte-anion channel VSOAC is regulated by nonhydrolytic ATP binding. Am. J. Physiol. 267 5 Pt 1 (1994) C1203-C1209
10. Jentsch T.J., Stein V., et al. Molecular structure and physiological function of chloride channels. Physiol. Rev. 82 2 (2002) 503-568
11. Jentsch T.J., Maritzen T., et al. Chloride channel diseases resulting from impaired transepithelial transport or vesicular function. J. Clin Invest 115 8 (2005) 2039-2046
12. Jones C.J., Bell C.L., et al. Different physiological signatures of sweat gland secretory and duct cells in culture. Am. J. Physiol. 255 1 Pt 1 (1988) C102-C111
13. Junqueira L.C., C.J., and Kelly R. Basic Histology (1998), Lange, New York
14. Kartner N., Augustinas O., et al. Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland. Nat. Genet 1 5 (1992) 321-327
15. Krouse M.E., Hagiwara G., et al. Ion channels in normal human and cystic fibrosis sweat gland cells. Am. J. Physiol. 257 1 Pt 1 (1989) C129-C140
16. Langbein L., Rogers M.A., et al. Characterization of a novel human type II epithelial keratin K1b, specifically expressed in eccrine sweat glands. J. Invest Dermatol. 125 3 (2005) 428-444
17. Lee C.M., and Dessi J. NCL-SG3: a human eccrine sweat gland cell line that retains the capacity for transepithelial ion transport. J. Cell Sci. 92 Pt 2 (1989) 241-249
18. Ma T., Thiagarajah J.R., et al. Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion. J. Clin Invest 110 11 (2002) 1651-1658
19. Mork A.C., and Roomans G.M. X-ray microanalysis of cAMP-induced ion transport in NCL-SG3 sweat gland cells. Scanning Microsc. 7 4 (1993) 1233-1239
20. Mork A.C., Hongpaisan J., et al. Ion transport in primary cultures from human sweat gland coils studied with X-ray microanalysis. Cell Biol. Int. 19 2 (1995) 151-159
21. Mork A.C., von Euler A., et al. cAMP-induced chloride transport in NCL-SG3 sweat gland cells. Acta Physiol Scand 157 1 (1996) 21-32
22. Munkonge F., Alton E.W., et al. Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicators. J. Cyst. Fibros. 3 2 (2004) 171-176
23. Novak I., Pedersen P.S., et al. Chloride and potassium conductances of cultured human sweat ducts. Pflugers Arch 422 2 (1992) 151-158
24. - channels in human epithelial cells. Jpn. J. Physiol. 44 Suppl. 2 (1994) S77-S79
25. Puljak L., and Kilic G. Emerging roles of chloride channels in human diseases. Biochim Biophys Acta 1762 4 (2006) 404-413
26. - impermeability in cystic fibrosis sweat duct epithelium. Am. J. Physiol. 257 4 Pt 1 (1989) C727-C735
27. - conductance in both cell membranes of an absorptive epithelium. J. Membr Biol. 130 1 (1992) 49-62
28. Reddy M.M., and Quinton P.M. Deactivation of CFTR-Cl conductance by endogenous phosphatases in the native sweat duct. Am. J. Physiol. 270 2 Pt 1 (1996) C474-C480
29. Reddy M.M., and Quinton P.M. Bumetanide blocks CFTR GCl in the native sweat duct. Am. J. Physiol. 276 1 Pt 1 (1999) C231-C237
30. Reddy M.M., Bell C.L., et al. Evidence of two distinct epithelial cell types in primary cultures from human sweat gland secretory coil. Am. J. Physiol. 262 4 Pt 1 (1992) C891-C898
31. Reddy M.M., Bell C.L., et al. Cystic fibrosis affects specific cell type in sweat gland secretory coil. Am. J. Physiol. 273 2 Pt 1 (1997) C426-C433
32. Ring A., Mork A.C., et al. Calcium-activated chloride fluxes in cultured NCL-SG3 sweat gland cells. Cell Biol. Int. 19 4 (1995) 265-278
33. Roland C.R., Nakafusa Y., et al. Gadolinium chloride inhibits lipopolysaccharide-induced mortality and in vivo prostaglandin E2 release by splenic macrophages. J. Gastrointest Surg 3 3 (1999) 301-307
34. Roomans G.M. Pharmacological approaches to correcting the ion transport defect in cystic fibrosis. Am. J. Respir Med. 2 5 (2003) 413-431
35. Sato K., Ohtsuyama M., et al. Whole cell K and Cl currents in dissociated eccrine secretory coil cells during stimulation. J. Membr. Biol. 134 2 (1993) 93-106
36. Sato F., Soos G., et al. Cystic fibrosis transport regulator and its mRNA are expressed in human epidermis. J. Invest Dermatol. 119 6 (2002) 1224-1230
37. Sorscher E.J., Kirk K.L., et al. Antisense oligodeoxynucleotide to the cystic fibrosis gene inhibits anion transport in normal cultured sweat duct cells. Proc. Natl. Acad Sci. U. S. A. 88 17 (1991) 7759-7762
38. Trapnell B.C., Chu C.S., et al. Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis. Proc. Natl. Acad Sci. U. S. A. 88 15 (1991) 6565-6569
39. Trapnell B.C., Zeitlin P.L., et al. Down-regulation of cystic fibrosis gene mRNA transcript levels and induction of the cystic fibrosis chloride secretory phenotype in epithelial cells by phorbol ester. J. Biol. Chem. 266 16 (1991) 10319-10323
40. - conductance in human sweat ducts. Exp. Physiol. 89 4 (2004) 417-425
41. Wilson S.M., Whiteford M.L., et al. The regulation of membrane 125I- and 86Rb+ permeability in a virally transformed cell line (NCL-SG3) derived from the human sweat gland epithelium. Exp. Physiol. 79 3 (1994) 445-459
42. Wilson S.M., Ko W.H., et al. Calcium-dependent regulation of membrane ion permeability in a cell line derived from the equine sweat gland epithelium. Comp. Biochem Physiol. A Physiol. 111 2 (1995) 215-221