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Airway epithelial integrity is protected by a long-acting beta2-adrenergic receptor agonist.

Abstract : Airway epithelial integrity may be impaired by bacterial exoproducts, which are able to degrade tight junction-associated proteins such as zonula occludens 1 (ZO-1). We have investigated the protective effect of salmeterol, a long-acting beta(2)-adrenergic agonist, on Pseudomonas aeruginosa-induced alteration of the epithelial junctional barrier. We demonstrate in human airway epithelial cells (HAEC) that salmeterol induces a time-dependent increase in ZO-1 protein, although no significant change in ZO-1 transcripts was observed. When HAEC cultures were exposed to P. aeruginosa (PAO1) supernatants, apical expression of ZO-1 protein was maintained in salmeterol-pretreated HAEC cultures, whereas it disappeared after PAO1 exposure in cultures not pretreated with salmeterol. Western blot experiments showed that the 220-kD ZO-1 protein was decreased after PAO1 incubation but was still present in salmeterol-pretreated HAEC extracts. The functional activity of ZO-1 protein was monitored by measuring transepithelial resistance and analyzing the diffusion of a low molecular weight tracer through the intercellular spaces. After PAO1 incubation, the epithelial integrity of HAEC was impaired, as shown by a decrease in transepithelial resistance and increased paracellular permeability, but was not significantly altered after salmeterol preincubation. These results demonstrate that salmeterol may contribute to the protection of the airway epithelium barrier against bacterial virulence factors.
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Contributor : Philippe Birembaut Connect in order to contact the contributor
Submitted on : Monday, May 14, 2007 - 9:04:59 AM
Last modification on : Thursday, October 14, 2021 - 1:10:03 PM




Christelle Coraux, Claire Kileztky, Myriam C. Polette, Jocelyne Hinnrasky, Jean-Marie Zahm, et al.. Airway epithelial integrity is protected by a long-acting beta2-adrenergic receptor agonist.. American Journal of Respiratory Cell and Molecular Biology, American Thoracic Society, 2004, 30 (5), pp.605-12. ⟨10.1165/rcmb.2003-0056OC⟩. ⟨inserm-00145972⟩



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