4.6 Article

Correlating genotype with phenotype using CFTR-mediated whole-cell Cl- currents in human nasal epithelial cells

Journal

JOURNAL OF PHYSIOLOGY-LONDON
Volume 600, Issue 6, Pages 1515-1531

Publisher

WILEY
DOI: 10.1113/JP282143

Keywords

CFTR chloride ion channel; cystic fibrosis; epithelial ion transport; genotype; human nasal epithelial cells; phenotype

Funding

  1. Vertex Innovation Award
  2. Vertex Pharmaceuticals (Europe) Ltd.

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This study investigates the relationship between genotype, phenotype, and CFTR function using human nasal epithelial cells, revealing differences in CFTR-mediated currents based on residual or minimal CFTR function. The findings suggest that CFTR expression and function are not affected by conditional reprogramming culture, and highlight the correlation between CFTR-mediated Cl- currents in hNE cells and sweat Cl- concentration, emphasizing the value of these cells in CFTR research and therapeutic testing.
Dysfunction of the epithelial anion channel cystic fibrosis transmembrane conductance regulator (CFTR) causes a wide spectrum of disease, including cystic fibrosis (CF) and CFTR-related diseases (CFTR-RDs). Here, we investigate genotype-phenotype-CFTR function relationships using human nasal epithelial (hNE) cells from a small cohort of non-CF subjects and individuals with CF and CFTR-RDs and genotypes associated with either residual or minimal CFTR function using electrophysiological techniques. Collected hNE cells were either studied directly with the whole-cell patch-clamp technique or grown as primary cultures at an air-liquid interface after conditional reprogramming. The properties of cAMP-activated whole-cell Cl- currents in freshly isolated hNE cells identified them as CFTR-mediated. Their magnitude varied between hNE cells from individuals within the same genotype and decreased in the rank order: non-CF > CFTR residual function > CFTR minimal function. CFTR-mediated whole-cell Cl- currents in hNE cells isolated from fully differentiated primary cultures were identical to those in freshly isolated hNE cells in both magnitude and behaviour, demonstrating that conditional reprogramming culture is without effect on CFTR expression and function. For the cohort of subjects studied, CFTR-mediated whole-cell Cl- currents in hNE cells correlated well with CFTR-mediated transepithelial Cl- currents measured in vitro with the Ussing chamber technique, but not with those determined in vivo with the nasal potential difference assay. Nevertheless, they did correlate with the sweat Cl- concentration of study subjects. Thus, this study highlights the complexity of genotype-phenotype-CFTR function relationships, but emphasises the value of conditionally reprogrammed hNE cells in CFTR research and therapeutic testing.

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