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Article has an altmetric score of 6

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Referenced in 4 patents
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Research Article Free access | 10.1172/JCI3214

Augmentation of lung liquid clearance via adenovirus-mediated transfer of a Na,K-ATPase beta1 subunit gene.

P Factor, F Saldias, K Ridge, V Dumasius, J Zabner, H A Jaffe, G Blanco, M Barnard, R Mercer, R Perrin, and J I Sznajder

Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Section of Pulmonary and Critical Care Medicine, Michael Reese Hospital, Chicago, Illinois 60616, USA. pfact@aol.com

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Published October 1, 1998 - More info

Published in Volume 102, Issue 7 on October 1, 1998
J Clin Invest. 1998;102(7):1421–1430. https://doi.org/10.1172/JCI3214.
© 1998 The American Society for Clinical Investigation
Published October 1, 1998 - Version history
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Abstract

Previous studies have suggested that alveolar Na,K-ATPases play an important role in active Na+ transport and lung edema clearance. We reasoned that overexpression of Na,K-ATPase subunit genes could increase Na,K-ATPase function in lung epithelial cells and edema clearance in rat lungs. To test this hypothesis we produced replication deficient human type 5 adenoviruses containing cDNAs for the rat alpha1 and beta1 Na,K-ATPase subunits (adMRCMValpha1 and adMRCMVbeta1, respectively). As compared to controls, adMRCMVbeta1 increased beta1 subunit expression and Na,K-ATPase function by 2. 5-fold in alveolar type 2 epithelial cells and rat airway epithelial cell monolayers. No change in Na,K-ATPase function was noted after infection with adMRCMValpha1. Rat lungs infected with adMRCMVbeta1, but not adMRCMValpha1, had increased beta1 protein levels and lung liquid clearance 7 d after tracheal instillation. Alveolar epithelial permeability to Na+ and mannitol was mildly increased in animals infected with adMRCMVbeta1 and a similar Escherichia coli lacZ-expressing virus. Our data shows, for the first time, that transfer of the beta1 Na,K-ATPase subunit gene augments Na,K-ATPase function in epithelial cells and liquid clearance in rat lungs. Conceivably, overexpression of Na,K-ATPases could be used as a strategy to augment lung liquid clearance in patients with pulmonary edema.

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Referenced in 4 patents
20 readers on Mendeley
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