Species-specific differences in mouse and human airway epithelial biology of recombinant adeno-associated virus transduction

X Liu, Z Yan, M Luo, JF Engelhardt - American journal of respiratory …, 2006 - atsjournals.org
X Liu, Z Yan, M Luo, JF Engelhardt
American journal of respiratory cell and molecular biology, 2006atsjournals.org
Differences in airway epithelial biology between mice and humans have presented
challenges to evaluating gene therapies for cystic fibrosis (CF) using murine models. In this
context, recombinant adeno-associated virus (rAAV) type 2 and rAAV5 vectors have very
different transduction efficiencies in human air–liquid interface (ALI) airway epithelia
(rAAV2≅ rAAV5) as compared with mouse lung (rAAV5>> rAAV2). It is unclear if these
differences are due to species-specific airway biology or limitations of ALI cultures to …
Differences in airway epithelial biology between mice and humans have presented challenges to evaluating gene therapies for cystic fibrosis (CF) using murine models. In this context, recombinant adeno-associated virus (rAAV) type 2 and rAAV5 vectors have very different transduction efficiencies in human air–liquid interface (ALI) airway epithelia (rAAV2 ≅ rAAV5) as compared with mouse lung (rAAV5 >> rAAV2). It is unclear if these differences are due to species-specific airway biology or limitations of ALI cultures to reproduce in vivo airway biology. To this end, we compared rAAV2 and rAAV5 transduction biology in mouse and human ALI cultures, and investigated the utility of murine ΔF508 cystic fibrosis transmembrane conductance regulator (CFTR) ALI epithelia to study CFTR complementation. Our results demonstrate that mouse ALI epithelia retain in vivo preferences for rAAV serotype transduction from the apical membrane (rAAV5 >> rAAV2) not seen in human epithelia (rAAV2 ≅ rAAV5). Viral binding of rAAV2 and rAAV5 to the apical surface of mouse ALI airway epithelia was not significantly different, and proteasome-modulating agents significantly enhanced rAAV2 transduction to a level equivalent to that of rAAV5 in the presence of these agents, suggesting that the ubiquitin/proteasome pathway represents a more significant intracellular block for rAAV2 transduction of mouse airway epithelia. Interestingly, cAMP-inducible chloride currents were enhanced in ΔF508CFTR mouse ALI cultures, making this model incompatible with CFTR complementation studies. These studies emphasize species-specific differences in airway biology between mice and humans that significantly influence the use of mice as surrogate models for rAAV transduction and gene therapy for CF.
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