Rhinovirus induction of the CXC chemokine epithelial-neutrophil activating peptide-78 in bronchial epithelium

被引:55
作者
Donninger, H
Glashoff, R
Haitchi, HM
Syce, JA
Ghildyal, R
van Rensburg, E
Bardin, PG
机构
[1] Univ Stellenbosch, Lung & Allergy Unit, Cape Town, South Africa
[2] Monash Med Ctr & Univ, Dept Resp & Sleep Med, Melbourne, Vic, Australia
关键词
D O I
10.1086/375246
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epithelial-neutrophil activating peptide-78 (ENA-78) induces neutrophil migration, an early response to viral infection. Rhinovirus serotype 16 (RV16) was used to infect primary bronchial epithelial cells and a cell line (BEAS-2B). Release of ENA-78 protein was measured by enzyme-linked immunosorbent assay, ENA-78 mRNA production was quantified by reverse-transcription polymerase chain reaction, and ENA-78 promoter activity was assessed by use of a promoter construct. After infection with RV16, ENA-78 protein and mRNA increased significantly, and RV16 induced 3-fold increases in ENA-78 gene transcription. Nasal ENA-78 measured in patients with asthma with and without RV infection was more elevated in patients with RV infection present. Our study demonstrates that ENA-78 is produced in bronchial epithelial cells in response to RV16 infection. With other chemokines, it may be an important initiator of neutrophil airway inflammation during RV common colds and thus may play a role in the development of virus-associated airway pathologies.
引用
收藏
页码:1809 / 1817
页数:9
相关论文
共 36 条
[1]   DETECTION OF RHINOVIRUS INFECTION OF THE NASAL-MUCOSA BY OLIGONUCLEOTIDE IN-SITU HYBRIDIZATION [J].
BARDIN, PG ;
JOHNSTON, SL ;
SANDERSON, G ;
ROBINSON, BS ;
PICKETT, MA ;
FRAENKEL, DJ ;
HOLGATE, ST .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (02) :207-213
[2]   Receptor binding specificity and pulmonary gene expression of the neutrophil-activating peptide ENA-78 [J].
Bozic, CR ;
Gerard, NP ;
Gerard, C .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (03) :302-308
[3]  
CHEN CA, 1988, BIOTECHNIQUES, V6, P632
[4]   RHINOVIRUS INHALATION CAUSES LONG-LASTING EXCESSIVE AIRWAY NARROWING IN RESPONSE TO METHACHOLINE IN ASTHMATIC SUBJECTS IN-VIVO [J].
CHEUNG, D ;
DICK, EC ;
TIMMERS, MC ;
DEKLERK, EPA ;
SPAAN, WJM ;
STERK, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (05) :1490-1496
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]   Interleukin-11: Stimulation in vivo and in vitro by respiratory viruses and induction of airways hyperresponsiveness [J].
Einarsson, O ;
Geba, GP ;
Zhu, Z ;
Landry, M ;
Elias, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) :915-924
[7]   Rhinovirus is associated with severe asthma exacerbations and raised nasal interleukin-12 [J].
Ferreira, A ;
Williams, Z ;
Donninger, H ;
van Schalkwyk, EM ;
Bardin, PG .
RESPIRATION, 2002, 69 (02) :136-142
[8]   Quantitative comparison of C-X-C chemokines produced by endotoxin-stimulated human alveolar macrophages [J].
Goodman, RB ;
Strieter, RM ;
Frevert, CW ;
Cummings, CJ ;
Tekamp-Olson, P ;
Kunkel, SL ;
Walz, A ;
Martin, TR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 275 (01) :L87-L95
[9]   Role of p38 mitogen-activated protein kinase in rhinovirus-induced cytokine production by bronchial epithelial cells [J].
Griego, SD ;
Weston, CB ;
Adams, JL ;
Tal-Singer, R ;
Dillon, SB .
JOURNAL OF IMMUNOLOGY, 2000, 165 (09) :5211-5220
[10]  
Grunberg K, 1997, AM J RESP CRIT CARE, V156, P609