Activation of vascular endothelial cells by IL-1α released by epithelial cells infected with respiratory syncytial virus

被引:29
作者
Chang, CH [1 ]
Huang, Y [1 ]
Anderson, R [1 ]
机构
[1] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4H7, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0008-8749(03)00058-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although pulmonary inflammation is a serious, sometimes life-threatening, consequence of respiratory syncytial virus (RSV) infection, the mechanisms involved are not well understood. Since the process of inflammation is initiated by a complex series of events including the activation of specific adhesion molecules on vascular endothelium, we searched for endothelial cell-activating factors released from RSV-infected epithelial cells. We demonstrate here that vascular endothelial cells exposed to culture supernatants from RSV-infected pulmonary epithelial A549 cells are activated to express increased cell surface ICAM-1, and to a lesser extent, VCAM-1 and E-selectin. IL-1alpha was identified as the predominant endothelial cell-activating factor by pretreating epithelial cell supernatants with anti-IL-1alpha antibody. The preferential upregulation of endothelial ICAM-1 (relative to VCAM-1 and E-selectin) by RSV-infected epithelia] cell supernatants was replicated by recombinant IL-1alpha thus confirming IL-1alpha as a major endothelial cell-activating cytokine released by RSV-infected epithelial cells. II-1alpha mediated endothelial cell activation is thus a likely contributory event in the initiation of leukocyte inflammation associated with RSV infection. Crown Copyright (C) 2003 Published by Elsevier Science (USA). All rights reserved.
引用
收藏
页码:37 / 41
页数:5
相关论文
共 31 条
[1]   Activation of endothelial cells via antibody-enhanced dengue virus infection of peripheral blood monocytes [J].
Anderson, R ;
Wang, SL ;
Osiowy, C ;
Issekutz, AC .
JOURNAL OF VIROLOGY, 1997, 71 (06) :4226-4232
[2]  
ARNOLD R, 1994, IMMUNOLOGY, V82, P126
[3]   EXPRESSION OF ADHESION MOLECULES (ICAM-1, LFA-3) ON HUMAN EPITHELIAL-CELLS (A549) AFTER RESPIRATORY SYNCYTIAL VIRUS-INFECTION [J].
ARNOLD, R ;
WERCHAU, H ;
KONIG, W .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (1-3) :392-393
[4]   INTERLEUKIN-8 EXPRESSION IN NORMAL NASAL EPITHELIUM AND ITS MODULATION BY INFECTION WITH RESPIRATORY SYNCYTIAL VIRUS AND CYTOKINES TUMOR-NECROSIS-FACTOR, INTERLEUKIN-1, AND INTERLEUKIN-6 [J].
BECKER, S ;
KOREN, HS ;
HENKE, DC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1993, 8 (01) :20-27
[5]  
BEVILACQUA MP, 1993, ANNU REV IMMUNOL, V11, P767, DOI 10.1146/annurev.iy.11.040193.004003
[6]   ULTRASTRUCTURAL FEATURES OF LESIONS IN BRONCHIOLAR EPITHELIUM IN INDUCED RESPIRATORY SYNCYTIAL VIRUS PNEUMONIA OF CALVES [J].
BRYSON, DG ;
PLATTEN, MF ;
MCCONNELL, S ;
MCNULTY, MS .
VETERINARY PATHOLOGY, 1991, 28 (04) :293-299
[7]  
CARLOS TM, 1994, BLOOD, V84, P2068
[8]   Interleukin-1α released from epithelial cells after adenovirus type 37 infection activates intercellular adhesion molecule 1 expression on human vascular endothelial cells [J].
Chang, CH ;
Huang, Y ;
Issekutz, AC ;
Griffith, M ;
Lin, KH ;
Anderson, R .
JOURNAL OF VIROLOGY, 2002, 76 (01) :427-431
[9]  
Couch Robert B., 1997, American Journal of Medicine, V102, P2, DOI 10.1016/S0002-9343(97)00003-X
[10]   Respiratory syncytial virus is an important cause of community-acquired lower respiratory infection among hospitalized adults [J].
Dowell, SF ;
Anderson, LJ ;
Gary, HE ;
Erdman, DD ;
Plouffe, JF ;
File, TM ;
Marston, BJ ;
Breiman, RF .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (03) :456-462