Cystic fibrosis (CF) is characterized by defective Cl⁻ and enhanced Na⁺ conductance, both due to malfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) protein in airway epithelial cells. In the present study we examined whether expression of CFTR mRNA (CFTR messenger ribonucleic acid) is different in airway epithelia derived from either CF patients or healthy volunteers. Moreover, we tried to correlate differences in epithelial Cl⁻ and Na⁺ conductance with the level of CFTR mRNA expression and studied whether these properties correlate to the clinical phenotype of CF patients. To that end, CFTR mRNA was determined by means of quantitative reverse transcriptase polymerase chain reaction (RT‐PCR) and cyclic adenosine monophosphate (cAMP)‐activated Cl⁻ and epithelial Na⁺ conductances were examined in airway epithelial cells using microelectrode techniques. Complementary in vitro data were obtained from cultured CF and non‐CF airway epithelial cell lines. Genotype and Shwachman score were assessed for each patient.

We found variable levels of CFTR mRNA expression in airway cells of both CF patients and healthy volunteers. As expected, epithelial Na⁺ conductance was enhanced and CFTR Cl⁻ conductance was absent in airway cells from CF patients. However, CFTR mRNA expression did not correlate with either electrophysiological properties or Shwachman scores obtained from CF patients. In addition, CFTR mRNA expression did not correlate to Cl⁻ conductance in cultured CF and non‐CF airway epithelial cells. These results indicate a lack of correlation between levels of CFTR mRNA and CFTR function, and that only small amounts of CFTR are required for expression of the CFTR Cl⁻ conductance. Pediatr Pulmonol. 1999; 27:251–259. © 1999 Wiley‐Liss, Inc.