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Title: Cystic fibrosis gene expression is not correlated with rectifying Cl sup minus channels

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America; (United States)
; ; ;  [1];  [2]
  1. Stanford Univ., CA (United States)
  2. Univ. of California, San Francisco (United States)

Cystic fibrosis (CF) involves a profound reduction of Cl{sup {minus}} permeability in several exocrine tissues. A distinctive, outwardly rectifying, depolarization-induced Cl{sup {minus}} channel (ORDIC channel) has been proposed to account for the Cl{sup {minus}} conductance that is defective in CF. The recently identified CF gene is predicted to code for a 1480-amino acid integral membrane protein termed the CF transmembrane conductance regulator (CFTR). The CFTR shares sequence similarity with a superfamily of ATP-binding membrane transport proteins such as P-glycoprotein and STE6, but it also has features consistent with an ion channel function. It has been proposed that the CFTR might be an ORDIC channel. To determine if CFTR and ORDIC channel expression are correlated, the authors surveyed various cell lines for natural variation in CFTR and ORDIC channel expression. In four human epithelial cell lines (T84, CaCo2, PANC-1, and 9HTEo-/S) that encompass the full observed range of CFTR mRNA levels and ORDIC channel density the authors found no correlation.

OSTI ID:
6101184
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America; (United States), Vol. 88:12; ISSN 0027-8424
Country of Publication:
United States
Language:
English