Gene transfer of CFTR to airway epithelia: low levels of expression are sufficient to correct Cl− transport and overexpression can generate basolateral CFTR
SL Farmen, PH Karp, P Ng, DJ Palmer… - … of Physiology-Lung …, 2005 - journals.physiology.org
American Journal of Physiology-Lung Cellular and Molecular …, 2005•journals.physiology.org
Gene transfer of CFTR cDNA to airway epithelia is a promising approach to treat cystic
fibrosis (CF). Most gene transfer vectors use strong viral promoters even though the
endogenous CFTR promoter is very weak. To learn whether expressing CFTR at a low level
in a fraction of cells would correct Cl− transport, we mixed freshly isolated wild-type and CF
airway epithelial cells in varying proportions and generated differentiated epithelia. Epithelia
with∼ 20% wild-type cells generated∼ 70% the transepithelial Cl− current of epithelia …
fibrosis (CF). Most gene transfer vectors use strong viral promoters even though the
endogenous CFTR promoter is very weak. To learn whether expressing CFTR at a low level
in a fraction of cells would correct Cl− transport, we mixed freshly isolated wild-type and CF
airway epithelial cells in varying proportions and generated differentiated epithelia. Epithelia
with∼ 20% wild-type cells generated∼ 70% the transepithelial Cl− current of epithelia …
Gene transfer of CFTR cDNA to airway epithelia is a promising approach to treat cystic fibrosis (CF). Most gene transfer vectors use strong viral promoters even though the endogenous CFTR promoter is very weak. To learn whether expressing CFTR at a low level in a fraction of cells would correct Cl− transport, we mixed freshly isolated wild-type and CF airway epithelial cells in varying proportions and generated differentiated epithelia. Epithelia with ∼20% wild-type cells generated ∼70% the transepithelial Cl− current of epithelia containing 100% wild-type cells. These data were nearly identical to those previously obtained with CFTR expressed under control of a strong promoter in a CF epithelial cell line. We also tested high level CFTR expression using the very strong cytomegalovirus (CMV) promoter as well as the cytokeratin-18 (K18) promoter. In differentiated airway epithelia, the CMV promoter generated 50-fold more transgene expression than the K18 promoter, but the K18 promoter generated more transepithelial Cl− current at high vector doses. Using functional studies, we found that with marked overexpression, some CFTR channels were present in the basolateral membrane where they shunted Cl− flow, thereby reducing net transepithelial Cl− transport. These results suggest that very little CFTR is required in a fraction of CF epithelial cells to complement Cl− transport because transepithelial Cl− flow is limited at the basolateral membrane. Thus they suggest a broad leeway in promoter strength for correcting the CF gene transfer, although at very high expression levels CFTR may be mislocalized to the basolateral membrane.
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