Literature DB >> 7680028

CFTR targeting in epithelial cells.

A P Morris1, S A Cunningham, R A Frizzell.   

Abstract

We used polarized and nonpolarized colonic cell lines (HT-29) to correlate CFTR function and expression with epithelial cell morphogenesis. Unpolarized cells express levels of CFTR mRNA and protein that are equivalent to those observed in polarized cells, and the extent of CFTR glycosylation is also similar. Despite these similarities in CFTR expression, the polarized cells secreted Cl in response to cAMP, but there was no cAMP-stimulated Cl conductance response in the unpolarized cells. In the polarized cells, CFTR is localized in the apical membrane domain, but in unpolarized cells the protein is retained at a perinuclear location. These findings indicate that a peripheral targeting mechanism, distal to the Golgi cisternae, controls the progression of N-linked glycoproteins like CFTR to the apical membrane. This targeting process does not become active until epithelial cells polarize. It may determine whether mutant forms of CFTR are targeted to the apical membrane.

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Year:  1993        PMID: 7680028     DOI: 10.1007/bf00768064

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  16 in total

1.  Intracellular accumulation and oligosaccharide processing of alkaline phosphatase under disassembly of the Golgi complex caused by brefeldin A.

Authors:  N Takami; K Oda; T Fujiwara; Y Ikehara
Journal:  Eur J Biochem       Date:  1990-12-27

2.  The cystic fibrosis gene has a "housekeeping"-type promoter and is expressed at low levels in cells of epithelial origin.

Authors:  K Yoshimura; H Nakamura; B C Trapnell; W Dalemans; A Pavirani; J P Lecocq; R G Crystal
Journal:  J Biol Chem       Date:  1991-05-15       Impact factor: 5.157

3.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

4.  Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Authors:  D P Rich; M P Anderson; R J Gregory; S H Cheng; S Paul; D M Jefferson; J D McCann; K W Klinger; A E Smith; M J Welsh
Journal:  Nature       Date:  1990-09-27       Impact factor: 49.962

5.  Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

Authors:  R J Gregory; S H Cheng; D P Rich; J Marshall; S Paul; K Hehir; L Ostedgaard; K W Klinger; M J Welsh; A E Smith
Journal:  Nature       Date:  1990-09-27       Impact factor: 49.962

6.  Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.

Authors:  M L Drumm; H A Pope; W H Cliff; J M Rommens; S A Marvin; L C Tsui; F S Collins; R A Frizzell; J M Wilson
Journal:  Cell       Date:  1990-09-21       Impact factor: 41.582

7.  In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator.

Authors:  A E Trezise; M Buchwald
Journal:  Nature       Date:  1991-10-03       Impact factor: 49.962

Review 8.  Cystic fibrosis: molecular biology and therapeutic implications.

Authors:  F S Collins
Journal:  Science       Date:  1992-05-08       Impact factor: 47.728

9.  Regulation of plasma membrane recycling by CFTR.

Authors:  N A Bradbury; T Jilling; G Berta; E J Sorscher; R J Bridges; K L Kirk
Journal:  Science       Date:  1992-04-24       Impact factor: 47.728

10.  Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR).

Authors:  C E Bear; C H Li; N Kartner; R J Bridges; T J Jensen; M Ramjeesingh; J R Riordan
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

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