RT Journal Article
SR Electronic
T1 Adhesion molecule expression on epithelial cells infected with respiratory syncytial virus
JF European Respiratory Journal
JO Eur Respir J
FD European Respiratory Society
SP 358
OP 366
DO 10.1034/j.1399-3003.2000.15b23.x
VO 15
IS 2
A1 SZ Wang
A1 PG Hallsworth
A1 KD Dowling
A1 JH Alpers
A1 JJ Bowden
A1 KD Forsyth
YR 2000
UL http://erj.ersjournals.com/content/15/2/358.abstract
AB Respiratory epithelium is both a target and an effector of airway inflammation. Adhesion molecules on epithelium play an important role in a variety of airway diseases. Respiratory syncytial virus (RSV) is the most important pathogen for airway diseases in infants. The expression of adhesion molecules on epithelium in RSV infection, however, is unclear. The expression of selected adhesion molecules and major histocompatibility complex (MHC) class I and II antigens on a human alveolar type II epithelial cell line (A549) infected with RSV was investigated by means of flow cytometry and immunocytochemistry. The results showed that intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) were expressed on A549 cells at a low level. E-cadherin and MHC class I antigen were constitutively expressed on the cells. RSV infection of A549 cells significantly upregulated the expression of ICAM-1, VCAM-1 and MHC class I and II antigens on these cells. RSV infection also altered the expression of E-cadherin on A549 cells. Immunostaining showed that E-cadherin was mainly upregulated around or in RSV-induced giant cells. These data suggest that respiratory syncytial virus infection of respiratory epithelial cells enhances the expression of adhesion molecules and major histocompatibility complex antigens. These changes may play an important role in the pathophysiology of respiratory syncytial virus disease.