Respiratory syncytial virus infection activates STAT signaling in human epithelial cells

被引:38
|
作者
Kong, XY
San Juang, H
Kumar, M
Behera, AK
Mohapatra, A
Hellermann, GR
Mane, S
Lockey, RF
Mohapatra, SS
机构
[1] Univ S Florida, Coll Med, Dept Internal Med,Div Allergy & Immunol, Joy McCann Culverhouse Airway Dis Ctr, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, Dept Med & Microbiol Immunobiol, H Lee Moffitt Canc Ctr, Tampa, FL 33682 USA
[3] VA Hosp, Tampa, FL USA
[4] Univ S Florida, H Lee Moffitt Canc Ctr, Coll Med, Funct Genom Core, Tampa, FL 33682 USA
关键词
respiratory syncytial virus; microarray; STAT; gene expression; signal transduction; transcription factors;
D O I
10.1016/S0006-291X(03)01008-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acute respiratory syncytial virus (RSV) infection causes airway inflammation and exacerbates asthma, but the mechanism of inflammation is poorly understood. The role of the STAT-signaling pathway in RSV infection in epithelial cells was examined in this study. DNA microarray analyses of RSV-infected human alveolar type II (A549) epithelial cells identified several genes whose expression was altered from -5.5 to +56.4-fold. Four of the highly expressed genes contained STAT-binding elements. In A549 and normal human bronchial epithelial cells (NHBE), RSV induced phosphorylation and nuclear translocation of STAT-1alpha that was abrogated when RSV attachment was blocked. Treatment with a JAK-2 inhibitor or transfection with dominant-negative STAT-1alpha blocked STAT-1alpha activation and RSV infection. RSV also activated STAT-3 and IL-6 specific antibodies blocked this activation. Thus, activation of the STAT-1alpha and STAT-3 pathways play a role in RSV infection. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:616 / 622
页数:7
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