Expression of nitric oxide synthase 2 and tumor necrosis factor α in swine naturally infected with Actinobacillus pleuropneumoniae

被引:19
作者
Cho, WS
Chae, C [2 ]
机构
[1] Seoul Natl Univ, Sch Agr Biotechnol, Suwon 441744, South Korea
[2] Seoul Natl Univ, Coll Vet Med, Dept Vet Pathol, Suwon 441744, South Korea
关键词
Actinobacillus pleuropneumoniae; inflammation; in situ hybridization; nitric oxide synthase 2; pigs; pneumonia; polymerase chain reaction; tumor necrosis factor alpha;
D O I
10.1354/vp.39-1-27
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Nitric oxide synthase 2 (NOS2) and tumor necrosis factor alpha (TNF-alpha) were detected and localized in 15 pigs with naturally occurring pleuropneumonia by use of in situ hybridization with a nonradioactive digoxigenin-labeled cDNA probe. Two cDNA probes 491 and 219 base pairs for NOS2 and TNF-alpha, respectively, were generated by reverse transcription polymerase chain reaction. All 15 pigs infected with Actinobacillus pleuropneumoniae had distinct positive hybridization signals for NOS2 and TNF-alpha. Strong hybridization signals for both NOS2 and TNF-alpha were evident in degenerate alveolar leukocytes bordering zones of coagulative necrosis and in alveolar spaces. NOS2 nucleic acids were detected in neutrophils and macrophages. In situ hybridization of serial sections of lung tissue revealed numerous cells positive for NOS2 and TNF-alpha, suggesting that NOS2 and TNF-alpha expression may play a role in the pathophysiology of pleuropneumonia.
引用
收藏
页码:27 / 32
页数:6
相关论文
共 31 条
[21]   Nitric oxide and macrophage function [J].
MacMicking, J ;
Xie, QW ;
Nathan, C .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :323-350
[22]   NITRIC-OXIDE SYNTHASE IN CIRCULATING VS EXTRAVASATED POLYMORPHONUCLEAR LEUKOCYTES [J].
MILES, AM ;
OWENS, MW ;
MILLIGAN, S ;
JOHNSON, GG ;
FIELDS, JZ ;
ING, TS ;
KOTTAPALLI, V ;
KESHAVARZIAN, A ;
GRISHAM, MB .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 58 (05) :616-622
[23]   Detection and distribution of DNA of Actinobacillus pleuropneumoniae in the lungs of naturally infected pigs by in-situ hybridization [J].
Min, K ;
Chae, C .
JOURNAL OF COMPARATIVE PATHOLOGY, 1998, 119 (02) :169-175
[24]  
MONCADA S, 1991, PHARMACOL REV, V43, P109
[25]   NITRIC-OXIDE AS A SECRETORY PRODUCT OF MAMMALIAN-CELLS [J].
NATHAN, C .
FASEB JOURNAL, 1992, 6 (12) :3051-3064
[26]   INFLAMMATION, IMMUNOREGULATION, AND INDUCIBLE NITRIC-OXIDE SYNTHASE [J].
NUSSLER, AK ;
BILLIAR, TR .
JOURNAL OF LEUKOCYTE BIOLOGY, 1993, 54 (02) :171-178
[27]   Inducible nitric oxide synthase expression in porcine immune cells [J].
Pampusch, MS ;
Bennaars, AM ;
Harsch, S ;
Murtaugh, MP .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 61 (2-4) :279-289
[28]   NITRIC-OXIDE SYNTHASE - MESSENGER-RNA EXPRESSION OF DIFFERENT ISOFORMS IN HUMAN MONOCYTES/MACROPHAGES [J].
REILING, N ;
ULMER, AJ ;
DUCHROW, M ;
ERNST, M ;
FLAD, HD ;
HAUSCHILDT, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (08) :1941-1944
[29]   PURIFICATION AND CHARACTERIZATION OF THE CYTOKINE-INDUCED MACROPHAGE NITRIC-OXIDE SYNTHASE - AN FAD-CONTAINING AND FMN-CONTAINING FLAVOPROTEIN [J].
STUEHR, DJ ;
CHO, HJ ;
KWON, NS ;
WEISE, MF ;
NATHAN, CF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7773-7777
[30]  
STUEHR DJ, 1992, ADV ENZYMOL RELAT AR, V65, P287