CFTR-dependent membrane insertion is linked to stimulation of the CFTR chloride conductance

American Journal of Physiology - Cell Physiology

Volumn 271, Issue 6 40-6, 1996, Pages

  Takahashi, Akira ^a   Watkins, Simon C ^a   Howard, Marybeth ^a   Frizzell, Raymond A ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

adenosine 3',5' cyclic monophosphate; capacitance; cystic fibrosis transmembrane conductance regulator; endocytosis; exocytosis

Indexed keywords

COMPLEMENTARY RNA; CYCLIC AMP; FORSKOLIN; ISOBUTYLMETHYLXANTHINE; MUTANT PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ANIMAL CELL; ARTICLE; CELL STIMULATION; CELL STRUCTURE; CELL SURFACE; CHLORIDE CONDUCTANCE; CHLORIDE CURRENT; CONTROLLED STUDY; MORPHOMETRICS; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; XENOPUS LAEVIS;

EID: 0030460582     PISSN: 03636143     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpcell.1996.271.6.c1887     Document Type: Article

References (39)

1. Anderson, M. P., H. A. Berger, D. P. Rich, R. J. Gregory, A. E. Smith, and M. J. Welsh. Nucleoside triphosphatases are required to open the CFTR chloride channel. Cell 67: 775-784, 1991.
2. Anderson, M. P., D. P. Rich, R. J. Gregory, A. E. Smith, and M. J. Welsh. Generation of cAMP-activated chloride currents by expression of CFTR. Science Wash. DC 251: 679-682, 1991.
3. Biwerski, J., and A. S. Verkman. Functional CFTR in endosomal compartment of CFTR-expressing fibroblasts and T84 cells. Am. J. Physiol. 266 (Cell Physiol. 35): C149-C156, 1994.
4. Boat, T. F., M. J. Welsh, and A. L. Beaudet. Cystic fibrosis. In: The Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1989, p. 2649-2680.
5. Bradbury, N. A., and R. J. Bridges. Role of membrane trafficking in plasma membrane solute transport. Am. J. Physiol. 267 (Cell Physiol. 36): C1-C24, 1994.
6. Bradbury, N. A., J. A. Cohn, C. J. Venglarik, and R. J. Bridges. Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles. J. Biol. Chem. 269: 8296-8302, 1994.
7. Bradbury, N. A., T. Jilling, G. Berta, E. J. Sorscher, R. J. Bridges, and K. L. Kirk. Regulation of plasma membrane recycling by CFTR. Science Wash. DC 256: 444-445, 1992.
8. + pumps in turtle-bladder luminal membrane: role of cell pH and calcium. Nature Lond. 314: 443-446, 1985.
9. Cheng, S. H., D. P. Rich, J. Marshall, R. J. Gregory, M. J. Welsh, and A. E. Smith. Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel. Cell 66: 1027-1036, 1991.
10. Corey, J. L., N. Davidson, H. A. Lester, N. Brecha, and M. W. Quick. Protein kinase C modulates the activity of a cloned γ-aminobutyric acid transporter expressed in Xenopus oocytes via regulated subcellular redistribution of the transporter. J. Biol. Chem. 269: 14759-14767, 1994.
11. Cunningham, S. A., R. T. Worrell, D. J. Benos, and R. A. Frizzell. cAMP-stimulated ion currents in Xenopus oocytes expressing CFTR cRNA. Am. J. Physiol. 262 (Cell Physiol. 31): C783-C788, 1992.
12. Deen, P. M. T., H. Croes, R. A. M. H. Van-Aubel, L. A. Ginsel, and C. H. Van-Os. Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing. J. Clin. Invest. 95: 2291-2296, 1995.
13. Dho, S., S. Grinstein, and J. Foskett. Plasma membrane recycling in CFTR-expressing CHO cells. Biochim. Biophys. Acta 225: 78-82, 1993.
14. Dersch, M. A., W. M. Bernent, C. A. Larabell, M. D. Mecca, and D. G. Capco. Cortical membrane-trafficking during the meiotic resumption of Xenopus laevis oocyte. Cell Tissue Res. 263: 375-383, 1991.
15. Drumm, M. L., D. L. Wilkinson, L. S. Smit, R. T. Worrell, T. V. Strong, R. A. Frizzell, D. C. Dawson, and F. S. Collins. Chloride conductance expressed by ΔF508 and other mutant CFTRs in Xenopus oocytes. Science Wash. DC 254: 1797-1799, 1991.
16. Fuller, C. M., H. H. Deetjen, A. Piper, and I. Schulz. Secretagogue and second messenger-activated Cl permeability in isolated pancreatic zymogen granules. Pfluegers Arch. 415: 29-36, 1989.
17. - conductance in HT29 cells. Pfluegers Arch. 424: 329-334, 1993.
18. Gregory, R. J., S. H. Cheng, D. P. Rich, J. Marshall, S. Paul, K. Hehir, L. Ostedgaard, K. W. Klinger, M. J. Welsh, and A. E. Smith. Expression and characterization of the cystic fibrosis transmembrane conductance regulator. Nature Lond. 347: 382-386, 1990.
19. Gurdon, J. B., and M. P. Wickens. The use of Xenopus oocytes for the expression of cloned genes. Methods Enzymol. 101: 370-386, 1983.
20. Hirst, B. H., and J. G. Forte. Redistribution and characterization of H/K-ATPase membranes from resting and stimulated gastric parietal cells. Biochem. J. 231: 641-649, 1985.
21. Howard, M., M. D. DuVall, D. C. Devor, J.-Y. Dong, K. Henze, and R. A. Frizzell. Epitope tagging permits cell surface detection of functional CFTR. Am. J. Physiol. 269 (Cell Physiol. 38): C1565-C1576, 1995.
22. Kuwahara, M., K. F. Kiyohide, Y. Terada, L. Bai, M. Fumiaki, and S. Sasaki. cAMP-dependent phosphorylation stimu-lates water permeability of aquaporin-collecting duct water channel protein expressed in Xenopus oocytes. J. Biol. Chem. 270: 10384-10387, 1995.
23. Lukacs, G. L., X. B. Chang, N. Kartner, O. D. Rotstein, J. R. Riordan, and S. Grinstein. The cystic fibrosis transmembrane conductance regulator is present and functional in endosomes: role as a determinant of endosomal pH. J. Biol. Chem. 267: 14568-14572, 1992.
24. Neher, E., and A. Marty. Discrete changes of cell membrane capacitance observed under conditions of enhanced secretion in bovine adrenal chromaffin cells. Proc. Natl. Acad. Sci. USA 79: 6712-6716, 1982.
25. Okada, Y., A. Hazama, A. Hashimoto, Y. Maruyama, and M. Kubo. Exocytosis upon osmotic swelling in human epithelial cells. Biochim. Biophys. Acta 1107: 201-205, 1992.
26. Peres, A., and G. Bernardini. The effective membrane capacity of Xenopus eggs: its relations with membrane conductance and cortical granule exocytosis. Pfluegers Arch. 404: 266-272, 1985.
27. Prat, A. G., Y. F. Xiao, D. A. Ausiello, and H. F. Cantiello. cAMP-independent regulation of CFTR by the actin cytoskel-eton. Am. J. Physiol. 268 (Cell Physiol. 37): C1552-C1561, 1995.
28. Prince, L. S., A. Tousson, and R. B. Marchase. Cell surface labeling of CFTR in T84 cells. Am. J. Physiol. 264 (Cell Physiol. 33): C491-C498, 1993.
29. Quinton, P. M., and M. M. Reddy. Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding. Nature. Lond. 360: 79-81, 1992.
30. Riordan, J. R., J. M. Rommens, B. Kerem, N. Alon, R. Rozmahel, Z. Grzelczak, J. Zielenski, S. Lok, N. Plavsic, and J. L. Chou. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science Wash. DC 245: 1066-1073, 1989.
31. Sadler, S. E., and J. L. Maller. In vivo regulation of cyclic AMP phosphodiesterase in Xenopus oocytes. Stimulation by insulin and insulin-like growth factor 1. J. Biol. Chem. 262: 10644-10650, 1987.
32. Santos, G. F., and W. W. Reenstra. Activation of the cystic fibrosis transmembrane regulator by cyclic AMP is not correlated with inhibition of endocytosis. Biochim. Biophys. Acta 1195: 96-102, 1994.
33. Stiefel, P., J. Peronine, and K. Simons. N-glycans as apical sorting signals in epithelial cells. Nature Lond. 378: 96-98, 1995.
34. Schwiebert, E. M., F. Gesek, L. Ercolani, C. Wjasow, D. C. Gruenert, K. Katherine, and B. A. Stanton. Heterotrimeric G proteins, vesicle trafficking, and CFTR Cl channels. Am. J. Physiol. 267 (Cell Physiol. 36): C272-C281, 1994.
35. Shibasaki, Y., T. Asano, J. L. Lin, K. Tsukuda, H. Katagiri, H. Ishihara, Y. Yazaki, and Y. Oka. Two glucose transporter isoforms are sorted differentially and are expressed in distinct cellular compartments. Biochem. J. 281: 829-834, 1992.
36. Sorscher, E. J., C. A. Fuller, R. J. Bridges, A. Tousson, R. B. Marchase, B. R. Brinkley, R. A. Frizzell, and D. J. Benos. Identification of a membrane protein from T84 cells using antibodies made against a DIDS-binding peptide. Am. J. Physiol. 262 (Cell Physiol. 31): C136-C147, 1992.
37. Suzuki, K., and T. Kono. Evidence that insulin causes translocation of glucose transport activity to the plasma membrane from an intracellular storage site. Proc. Natl. Acad. Sci. USA 114: 1113-1124, 1980.
38. Tabcharani, J. A., X. B. Chang, J. R. Riordan, and J. W. Hanrahan. Phosphorylation regulated Cl channel in CHO cells stably expressing the cystic fibrosis gene. Nature Lond. 352: 628-631, 1991.
39. Webster, P., L. Vanacore, A. Nairn, and C. R. Marino. Subcellular localization of CFTR to endosomes in a ductal epithelium. Am. J. Physiol. 267 (Cell Physiol. 36): C340-C348, 1994.