help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on October 23, 2008, doi:10.1165/rcmb.2008-0034OC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2008-0034OCv1
40/5/588    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Related articles in AJRCMB
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chen, L.
Right arrow Articles by Matalon, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chen, L.
Right arrow Articles by Matalon, S.
American Journal of Respiratory Cell and Molecular Biology. Vol. 40, pp. 588-600, 2009
© 2009 American Thoracic Society
DOI: 10.1165/rcmb.2008-0034OC

Inhibition of Na+ Transport in Lung Epithelial Cells by Respiratory Syncytial Virus Infection

Lan Chen1, Weifeng Song1,2, Ian C. Davis1,*, Kedar Shrestha1, Erik Schwiebert2,3, Wayne M. Sullender2,4 and Sadis Matalon1,2,5

Departments 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 {alpha}- but not {gamma}-ENaC subunit protein levels at 24 hours after RSV infection. The reduction in amiloride-sensitive Isc in H441 cells was prevented by pretreatment with inhibitors of de novo pyrimidine or purine synthesis (A77-1726 and 6-MP, respectively, 50 µM). Our results suggest that infection of both murine and human respiratory epithelial cells with RSV inhibits vectorial Na+ transport via nucleotide release. These findings are consistent with our previous studies showing reduced alveolar fluid clearance after RSV infection of BALB/c mice.

Key Words: short circuit current • epithelial Na+ channels • H441 cells • uridine triphosphate • A77-1726


CLINICAL RELEVANCE

Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract disease in infants and children worldwide. We have conducted in vitro studies to elucidate the mechanisms by which RSV causes fluid accumulation in the lungs.

 

Related articles in AJRCMB:

Highlights of the May Issue
Kenneth B. Adler and Sadis Matalon
AJRCMB 2009 40: 505-506. [Full Text]  



This article has been cited by other articles:


Home page
Am. J. Respir. Cell Mol. Bio.Home page
K. B. Adler and S. Matalon
Highlights of the September Issue
Am. J. Respir. Cell Mol. Biol., September 1, 2009; 41(3): 249 - 250.
[Full Text] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
K. B. Adler and S. Matalon
Highlights of the May Issue
Am. J. Respir. Cell Mol. Biol., May 1, 2009; 40(5): 505 - 506.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2009 American Thoracic Society.
  CCM abstracts