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| MOLECULAR-BASIS OF DEFECTIVE ANION TRANSPORT IN L-CELLS EXPRESSING RECOMBINANT FORMS OF CFTR |
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| Author(s): YANG YP, DEVOR DC, ENGELHARDT JF, ERNST SA, STRONG TV, COLLINS FS, COHN JA, FRIZZELL RA, WILSON JM |
| Source: HUMAN MOLECULAR GENETICS Volume: 2 Issue: 8 Pages: 1253-1261 Published: AUG 1993 |
| Times Cited: 55 References: 34 |
| Abstract: Cystic fibrosis (CF) is caused by mutations in the gene encoding a chloride channel called the CF transmembrane conductance regulator (CFTR). A single mutation in this gene, deletion of three nucleotides that leads to the absence of phenylalanine 508 (i.e., DELTAF508), is found on 70% of all CF chromosomes. To explore the molecular mechanism(s) responsible for defective chloride transport in patients with CF, we have studied the processing, localization, and function of wild type (W.T.), DELTAF508 and G551D CFTR (a G-->D missense mutation at position 551) in retrovirus transduced L cells. Cell transduced with W.T. CFTR expressed a 170 kd CFTR protein that was endoglycosidase H (Endo H) resistant, localized to the plasma membrane, and generated a cAMP-mediated anion conductance (G(Cl)) when stimulated with standard concentrations of forskolin (5 muM), cpt cAMP (400 muM) and IBMX (100 muM). The G551D CFTR was indistinguishable from W.T. CFTR with respect to post-translational processing and localization, but it did not produce a cAMP-activated G(Cl) in response to the standard stimulation cocktail. However, raising the IBMX concentration to 4 mM produced G(Cl) in G551D expressing cells. Cells transduced with DELTAF508 CFTR expressed an Endo H sensitive CFTR protein (approximately 140 kd) that was found in a cytosolic, perinuclear location. These cells did not respond to the standard cocktail, but approximately 20% of cells increased G(Cl) when the cocktail contained 4 mM IBMX. Incubation of cells at 26-degrees-C for 48 hours prior to analysis elicited responses in DELTAF508 expressing cells at low IBMX concentrations, but had no effect on the responses of cells expressing W.T. or G551D CFTR. The response of DELTAF508 to 26-degrees-C was associated with plasma membrane localization of CFTR protein. These results suggest that there are two mechanisms whereby CFTR mutations lead to loss of cAMP-responsive G(Cl). First, shown by G551D CFTR, the protein can be processed and targeted to the plasma membrane correctly, but lack full responsiveness to stimulation by cAMP. Second, as examplified by DELTAF508 CFTR, a partially functional protein which is not targeted to its correct cellular location can also lead to loss of the cAMP-responsive G(Cl). |
| Document Type: Article |
| Language: English |
Addresses:
1. UNIV MICHIGAN, DEPT INTERNAL MED, ANN ARBOR, MI 48109 USA
2. UNIV MICHIGAN, DEPT BIOL CHEM, ANN ARBOR, MI 48109 USA
3. UNIV MICHIGAN, DEPT ANAT & CELL BIOL, ANN ARBOR, MI 48109 USA
4. UNIV MICHIGAN, DEPT HUMAN GENET, ANN ARBOR, MI 48109 USA
5. DUKE UNIV, DEPT MED, DURHAM, NC 27706 USA
6. VET ADM MED CTR, DURHAM, NC 27705 USA
7. UNIV ALABAMA, DEPT PHYSIOL & BIOPHYS, BIRMINGHAM, AL 35294 USA |
| Publisher: OXFORD UNIV PRESS UNITED KINGDOM, WALTON ST JOURNALS DEPT, OXFORD, ENGLAND OX2 6DP |
| Subject Category: Biochemistry & Molecular Biology; Genetics & Heredity |
| IDS Number: LV836 |
| ISSN: 0964-6906 |
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