Transcription in response to physical stress -: clues to the molecular mechanisms of exercise-induced asthma

被引:32
作者
Hilberg, T
Deigner, HP
Möller, E
Claus, RA
Ruryk, A
Gläser, D
Landre, JBP
Brunkhorst, FM
Reinhart, K
Gabriel, HHW
Russwurm, S
机构
[1] Univ Jena, Sch Chem Sci, D-07749 Jena, Germany
[2] Univ Jena, Dept Sports Med, Wollnitzerstr 42, D-07749 Jena, Germany
[3] SIRS Lab GmbH, Jena, Germany
[4] Univ Hosp Jena, Dept Anesthesiol & Intens Care Med, Jena, Germany
关键词
microarray; leukotriene; acute-phase response; gene expression;
D O I
10.1096/fj.04-3063fje
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
To clarify stress-induced immunological reactions and molecular events during exercise and the potential relevance to exercise-induced bronchoconstriction, transcriptional responses to standardized physical stress were determined. Six healthy, young volunteers underwent an endurance exercise of 90% of their individual anaerobic threshold for 90 min. Time-dependent alterations in the expression pattern of leukocytes from healthy, trained subjects were analyzed by DNA microarrays before and 2 h and 6 h after exercise. Starting out from a large collection of cDNA library clones comprising more than 70,000 human expressed sequence tags, we selected, designed, and immobilized oligonucleotide probes (60-70mers) for transcripts of 5000 stress and inflammation-relevant genes. Exercise-induced stress provoked changes in the expression of 433 gene activities 2 h and/or 6 h after exercise, which could be grouped into six clusters. The most prominent feature was an enhanced transcription of two genes, coding for 5-lipoxygenase (ALOX5) and ALOX5-activating protein. Moreover, enhanced levels of leukotriene B-4 (LTB4) and LTC4 (P < 0.05) were detected in plasma after exercise. Our data demonstrate that exercise alters the activities of a distinct number of genes. In particular, they possibly provide novel insights into the molecular mechanisms of exercise-induced bronchoconstriction and suggest that enhanced transcription of ALOX5 and its activating protein together with a present predisposition of the subject critically contribute to exercise-induced asthma.
引用
收藏
页码:1492 / +
页数:20
相关论文
共 46 条
[1]  
[Anonymous], 2003, Design and Analysis of DNA Microarray Investigations
[2]  
[Anonymous], 2003, STAT APPL GENET MOL
[3]   ENHANCED GENERATION OF LEUKOTRIENE-B4 BY NEUTROPHILS STIMULATED BY UNOPSONIZED ZYMOSAN AND BY CALCIUM IONOPHORE AFTER EXERCISE-INDUCED ASTHMA [J].
ARM, JP ;
HORTON, CE ;
HOUSE, F ;
CLARK, TJH ;
SPUR, BW ;
LEE, TH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 138 (01) :47-53
[4]  
Ball CA, 2002, SCIENCE, V298, P539
[5]   Interleukin-6 is an essential, corticotropin-releasing hormone-independent stimulator of the adrenal axis during immune system activation [J].
Bethin, KE ;
Vogt, SK ;
Muglia, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :9317-9322
[6]   Strenuous exercise increases plasmatic and urinary leukotriene E4 in cyclists [J].
Caillaud, C ;
Le Creff, C ;
Legros, P ;
Denjean, A .
CANADIAN JOURNAL OF APPLIED PHYSIOLOGY-REVUE CANADIENNE DE PHYSIOLOGIE APPLIQUEE, 2003, 28 (06) :793-806
[7]   Interleukin-6 production by human neutrophils after Fc-receptor cross-linking or exposure to granulocyte colony-stimulating factor [J].
Ericson, SG ;
Zhao, Y ;
Gao, HL ;
Miller, KL ;
Gibson, LF ;
Lynch, JP ;
Landreth, KS .
BLOOD, 1998, 91 (06) :2099-2107
[8]  
Febbraio MA, 2003, EXERC IMMUNOL REV, V9, P34
[9]  
Fehrenbach E, 2003, EXERC IMMUNOL REV, V9, P58
[10]   TUMOR-NECROSIS-FACTOR - CHARACTERIZATION AT THE MOLECULAR, CELLULAR AND INVIVO LEVEL [J].
FIERS, W .
FEBS LETTERS, 1991, 285 (02) :199-212