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Targeting the urokinase plasminogen activator receptor enhances gene transfer to human airway epithelia
Paola T. Drapkin, Catherine R. O’Riordan, Su Min Yi, John A. Chiorini, Jonathan Cardella, Joseph Zabner, Michael J. Welsh
Paola T. Drapkin, Catherine R. O’Riordan, Su Min Yi, John A. Chiorini, Jonathan Cardella, Joseph Zabner, Michael J. Welsh
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Article

Targeting the urokinase plasminogen activator receptor enhances gene transfer to human airway epithelia

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Abstract

Developing gene therapy for cystic fibrosis has been hindered by limited binding and endocytosis of vectors by human airway epithelia. Here we show that the apical membrane of airway epithelia express the urokinase plasminogen activator receptor (uPAR). Urokinase plasminogen activator (uPA), or a 7-residue peptide derived from this protein (u7-peptide), bound the receptor and stimulated apical endocytosis. Both ligands enhanced gene transfer by nonspecifically bound adenovirus and adeno-associated virus vectors and by a modified adenovirus vector that had been coupled to the u7-peptide. These data provide the first evidence that targeting an apical receptor can circumvent the two most important barriers to gene transfer in airway epithelia. Thus, the uPA/uPAR system may offer significant advantages for delivering genes and other pharmaceuticals to airway epithelia.

Authors

Paola T. Drapkin, Catherine R. O’Riordan, Su Min Yi, John A. Chiorini, Jonathan Cardella, Joseph Zabner, Michael J. Welsh

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Figure 1

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Expression of uPAR in differentiated human airway epithelia. FACS analys...
Expression of uPAR in differentiated human airway epithelia. FACS analysis of uPAR staining in COS-1 cells (a) and differentiated human airway epithelia (b). (c) Projection of 180-μm thick X-Z series of confocal images. Green is staining from anti-uPAR antibody and red is ethidium bromide fluorescence to identify cells. (d) Western blot for uPAR. Lane A is from MDAMB231 cells, lane B is from H441 cells, and lane C is from human airway epithelia. uPAR migrates at ∼55 kDa.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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