Published ahead of print on October 23, 2008, doi:10.1165/rcmb.2008-0034OC
© 2009 American Thoracic Society DOI: 10.1165/rcmb.2008-0034OC Inhibition of Na+ Transport in Lung Epithelial Cells by Respiratory Syncytial Virus InfectionDepartments of 1 Anesthesiology, 4 Pediatrics, 5 Physiology and Biophysics, and 2 Pulmonary Injury and Repair Center, University of Alabama at Birmingham, Birmingham, Alabama; and 3 DiscoveryBioMed, LLC, Birmingham, Alabama Correspondence and requests for reprints should be addressed to Sadis Matalon, Ph.D., Department of Anesthesiology, University of Alabama at Birmingham, 224 BMR II, 901 South 19th Street, Birmingham, AL 35205-3703. E-mail: sadis{at}uab.edu
We investigated the mechanisms by which respiratory syncytial virus (RSV) infection decreases vectorial Na+ transport across respiratory epithelial cells. Mouse tracheal epithelial (MTE) cells from either BALB/c or C57BL/6 mice and human airway H441 cells were grown on semipermeable supports under an air–liquid interface. Cells were infected with RSV-A2 and mounted in Ussing chambers for measurements of short-circuit currents (Isc). Infection with RSV for 24 hours (multiplicity of infection = 1) resulted in positive immunofluorescence for RSV antigen in less than 10% of MTE or H441 cells. In spite of the limited number of cells infected, RSV reduced both basal and amiloride-sensitive Isc in both MTE and H441 cells by approximately 50%, without causing a concomitant reduction in transepithelial resistance. Agents that increased intracellular cAMP (forskolin, cpt-CAMP, and IBMX) increased mainly Cl– secretion in MTE cells and Na+ absorption in H441 cells. RSV infection for 24 hours blunted both variables. In contrast, ouabain sensitive Isc, measured across apically permeabilized H441 monolayers, remained unchanged. Western blot analysis of H441 cell lysates demonstrated reductions in
Key Words: short circuit current epithelial Na+ channels H441 cells uridine triphosphate A77-1726
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