Related Content
Search Google Scholar for:
|
|
Science 23 June 1989: Vol. 244. no. 4911, pp. 1472 - 1475 DOI: 10.1126/science.2472008
|
|
Articles
Science, Vol 244, Issue 4911, 1472-1475
Copyright © 1989 by American Association for the Advancement of Science
Persistence of abnormal chloride conductance regulation in transformed cystic fibrosis epithelia
AM Jetten,
Yankaskas JR,
MJ Stutts,
NJ Willumsen,
and
RC Boucher
National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
An airway epithelial cell line (CF/T43) was developed by infecting cultured airway epithelial cells from patients with cystic fibrosis (CF) with the pZIPneoSV(X)1/SV40T retrovirus and selecting for G418 resistance and ion transport properties. The distinctive chloride secretory phenotypes of the CF cell line CF/T43 and a normal cell line (NL/T4) were not perturbed by SV40T-induced cell transformation. Epithelial cell lines generated from CF cells with the SV40T gene can be used to test candidate CF genes and to evaluate the molecular mechanisms responsible for the CF phenotype.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
- Generation and phenotype of cell lines derived from CF and non-CF mice that carry the H-2Kb-tsA58 transgene.
- M. Takacs-Jarrett, W. E. Sweeney, E. D. Avner, and C. U. Cotton (2001)
Am J Physiol Cell Physiol
280, C228-C236
| Abstract »
| Full Text »
| PDF »
- Reduced Interleukin-8 Production by Cystic Fibrosis Airway Epithelial Cells.
- A.R. D. Massengale, F. Quinn Jr., J. Yankaskas, D. Weissman, W. Thomas McClellan, C. Cuff, and S. C. Aronoff (1999)
Am. J. Respir. Cell Mol. Biol.
20, 1073-1080
| Abstract »
| Full Text »
- Enhanced Efficiency of Lactosylated Poly-L-Lysine-Mediated Gene Transfer into Cystic Fibrosis Airway Epithelial Cells.
- W. J. W. Kollen, F. M. Schembri, G. J. Gerwig, J. F. G. Vliegenthart, M. C. Glick, and T. F. Scanlin (1999)
Am. J. Respir. Cell Mol. Biol.
20, 1081-1086
| Abstract »
| Full Text »
- CFTR Is a Conductance Regulator as well as a Chloride Channel.
- E. M. SCHWIEBERT, D. J. BENOS, M. E. EGAN, M. J. STUTTS, and W. B. GUGGINO (1999)
Physiol Rev
79, 145-166
| Abstract »
| Full Text »
| PDF »
- Factors Influencing Adeno-Associated Virus-Mediated Gene Transfer to Human Cystic Fibrosis Airway Epithelial Cells: Comparison with Adenovirus Vectors.
- S. Teramoto, J. S. Bartlett, D. McCarty, X. Xiao, R. J. Samulski, and R. C. Boucher (1998)
J. Virol.
72, 8904-8912
| Abstract »
| Full Text »
| PDF »
- Morphological and functional characterization of a conditionally immortalized collecting tubule cell line.
- M. Takacs-Jarrett, W. E. Sweeney, E. D. Avner, and C. U. Cotton (1998)
Am J Physiol Renal Physiol
275, F802-F811
| Abstract »
| Full Text »
| PDF »
- Bioelectric Properties of Gerbil Middle Ear Epithelia.
- L. M. de Serres, M. R. Van Scott, H. C. Pillsbury, and J. Prazma (1991)
Arch Otolaryngol Head Neck Surg
117, 416-421
| Abstract »
| PDF »
- Cell cycle dependence of chloride permeability in normal and cystic fibrosis lymphocytes.
- J. Bubien, K. Kirk, T. Rado, and R. Frizzell (1990)
Science
248, 1416-1419
| Abstract »
| PDF »
- Identification of the cystic fibrosis gene: chromosome walking and jumping.
- J. Rommens, M. Iannuzzi, B Kerem, M. Drumm, G Melmer, M Dean, R Rozmahel, J. Cole, D Kennedy, N Hidaka, et al. (1989)
Science
245, 1059-1065
| Abstract »
| PDF »
- The basic defect in cystic fibrosis.
- I. Levitan (1989)
Science
244, 1423
| PDF »
|
|