5-lipoxygenase products are necessary for ovalbumin-induced airway responsiveness in mice

被引:122
作者
Irvin, CG
Tu, YP
Sheller, JR
Funk, CD
机构
[1] VANDERBILT UNIV, DEPT MED, NASHVILLE, TN 37232 USA
[2] VANDERBILT UNIV, DEPT PHARMACOL, NASHVILLE, TN 37232 USA
[3] NATL JEWISH CTR IMMUNOL & RESP MED, DEPT MED, DENVER, CO 80206 USA
关键词
eosinophil; immunoglobulin; leukotrienes;
D O I
10.1152/ajplung.1997.272.6.L1053
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To determine the role of 5-lipoxygenase products in the development of airway reactivity that follows antigen exposure, we sensitized mice by intraperitoneal injection of ovalbumin and aluminum hydroxide and serial exposure to aerosols of ovalbumin. Mice lacking a functioning B-lipoxygenase enzyme were produced by targeted gene disruption. They and their wild-type controls had measurements of lung resistance (R-L) made in response to intravenous methacholine; bronchoalveolar lavage fluid cell counts and serum immunoglobulin concentrations were also measured. Wildtype mice developed striking increases in cholinergic responsiveness; 5-lipoxygenase-deficient mice manifested minimal alterations in methacholine responsiveness (R-L at the highest methacholine dose was 9.9 +/- 2.4 cmH(2)O . ml(-1).s(-1) under control conditions vs. 27.6 +/- 4.6 cmH(2)O . ml(-1).s(-1) after ovalbumin in wild-type mice; 5.9 +/- 0.9 vs. 7.01 +/- 2.2 cmH(2)O . ml(-1).s(-1) in 5-lipoxygenase-deficient mice). Ovalbumin provoked airway eosinophilia and increased immunoglobulins in wild-type mice, which were present to a significantly lesser degree in 5-lipoxygenase-deficient mice. We conclude that 5-lipoxygenase products are essential for the production of nonspecific airway reactivity in mice and suggest that 5-lipoxygenase products may be important in immunoglobulin formation.
引用
收藏
页码:L1053 / L1058
页数:6
相关论文
共 29 条
[1]  
BOUSHEY HA, 1980, AM REV RESPIR DIS, V121, P389
[2]   ATTENUATION OF ALLERGIC AIRWAY INFLAMMATION IN IL-4 DEFICIENT MICE [J].
BRUSSELLE, GG ;
KIPS, JC ;
TAVERNIER, JH ;
VANDERHEYDEN, JG ;
CUVELIER, CA ;
PAUWELS, RA ;
BLUETHMANN, H .
CLINICAL AND EXPERIMENTAL ALLERGY, 1994, 24 (01) :73-80
[3]   CDNA CLONING, EXPRESSION, MUTAGENESIS, INTRACELLULAR-LOCALIZATION, AND GENE CHROMOSOMAL ASSIGNMENT OF MOUSE 5-LIPOXYGENASE [J].
CHEN, XS ;
NAUMANN, TA ;
KURRE, U ;
JENKINS, NA ;
COPELAND, NG ;
FUNK, CD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17993-17999
[4]   ROLE OF LEUKOTRIENES REVEALED BY TARGETED DISRUPTION OF THE 5-LIPOXYGENASE GENE [J].
CHEN, XS ;
SHELLER, JR ;
JOHNSON, EN ;
FUNK, CD .
NATURE, 1994, 372 (6502) :179-182
[5]   Interleukin 4, but not interleukin 5 or eosinophils, is required in a murine model of acute airway hyperreactivity [J].
Corry, DB ;
Folkesson, HG ;
Warnock, ML ;
Erle, DJ ;
Matthay, MA ;
WienerKronish, JP ;
Locksley, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :109-117
[6]  
CROSFILL ML, 1961, J PHYSIOL-LONDON, V158, P1, DOI 10.1113/jphysiol.1961.sp006750
[7]   PEPTIDO-LEUKOTRIENES ARE POTENT AGONISTS OF VON-WILLEBRAND-FACTOR SECRETION AND P-SELECTIN SURFACE EXPRESSION IN HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS [J].
DATTA, YH ;
ROMANO, M ;
JACOBSON, BC ;
GOLAN, DE ;
SERHAN, CN ;
EWENSTEIN, BM .
CIRCULATION, 1995, 92 (11) :3304-3311
[8]   QUANTITATIVE LOCUS ANALYSIS OF AIRWAY HYPERRESPONSIVENESS IN A/J AND C57BL/6J MICE [J].
DESANCTIS, GT ;
MERCHANT, M ;
BEIER, DR ;
DREDGE, RD ;
GROBHOLZ, JK ;
MARTIN, TR ;
LANDER, ES ;
DRAZEN, JM .
NATURE GENETICS, 1995, 11 (02) :150-154
[9]   TREATMENT OF CHRONIC STABLE ASTHMA WITH DRUGS ACTIVE ON THE 5-LIPOXYGENASE PATHWAY [J].
DRAZEN, JM ;
ISRAEL, E .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (1-3) :319-320
[10]   Sorting out the cytokines of asthma [J].
Drazen, JM ;
Arm, JP ;
Austen, KF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (01) :1-5