Cytokine profiles following interaction between bovine alveolar macrophages and Pasteurella haemolytica

被引:34
作者
Morsey, MA [1 ]
Van-Kessel, AG [1 ]
Mori, Y [1 ]
Popowych, Y [1 ]
Godson, D [1 ]
Campos, M [1 ]
Babiuk, LA [1 ]
机构
[1] Pfizer Inc, Groton, CT 06340 USA
基金
英国医学研究理事会;
关键词
Pasteurella haemolytica; shipping fever; cytokine; pathogenesis;
D O I
10.1006/mpat.1999.0274
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pasteurella haemolytica is a Gram negative bacterium frequently isolated from the lungs of calves suffering from a fibrinous pneumonic condition known as shipping fever. To understand the pathogenesis of this disease, we investigated the induction of cytokin gene expression in cultures of bovine alveolar macrophages (BAM) stimulated with heat-killed Fl haemolytica. Northern blot analysis of total RNA showed that P. haemolytica induced early, abundant, and consistent synthesis of IL-1, TNF-alpha, and IL-8 mRNA. Cytokine mRNAs were detected within 1 hr post-stimulation with heat-killed P. haemolytica. IL-1 and IL-8 mRNA accumulated to high levels with increase in stimulation time, whereas TNF-alpha mRNA clearly declined by 4 and 8 h post stimulation. IL-1,TNF-alpha, and IL-8 proteins were also secreted into the culture medium of BAM stimulated with heat-killed P. haemolytica. All three proteins were detected at high levels 8 and 12 h post stimulation with P. haemolytica. BAM cells treated with bovine interferon-alpha and then stimulated with Fl haemolytica produced higher amounts of IL-1, IL-8 and TNF-alpha proteins compared to BAM stimulated with P. haemolytica alone. These findings demonstrate the powerful and selective induction of cytokine mRNA and protein synthesis in BAM stimulated with heat-killed P. haemolytica and may explain certain aspects of shipping fever pathogenesis. (C) 1999 Academic Press.
引用
收藏
页码:325 / 331
页数:7
相关论文
共 18 条
[1]  
ANGUS T, 1991, CYTOKINE HDB
[2]   EFFECT OF BOVINE ALPHA-1-INTERFERON ON BOVINE HERPESVIRUS TYPE-1-INDUCED RESPIRATORY-DISEASE [J].
BABIUK, LA ;
OHMANN, HB ;
GIFFORD, G ;
CZARNIECKI, CW ;
SCIALLI, VT ;
HAMILTON, EB .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 (NOV) :2383-2394
[3]  
CHANG YF, 1986, AM J VET RES, V47, P716
[4]  
CONFER AW, 1990, CAN J VET RES, V54, pS48
[5]  
DULK D, 1981, METHODS STUDYING MON, P258
[6]  
DYER RM, 1982, COMPEND CONTIN EDU, V4, P296
[7]   CAPTURE IMMUNOASSAY FOR RUMINANT TUMOR-NECROSIS-FACTOR-ALPHA - COMPARISON WITH BIOASSAY [J].
ELLIS, JA ;
GODSON, D ;
CAMPOS, M ;
SILEGHEM, M ;
BABIUK, LA .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1993, 35 (3-4) :289-300
[8]   BOVINE ALVEOLAR MACROPHAGE .1. ISOLATION, IN-VITRO CULTIVATION, ULTRASTRUCTURE, AND PHAGOCYTOSIS [J].
FOX, ML .
CANADIAN JOURNAL OF MICROBIOLOGY, 1973, 19 (10) :1207-&
[9]   RE-EXAMINATION AND FURTHER DEVELOPMENT OF A PRECISE AND RAPID DYE METHOD FOR MEASURING CELL-GROWTH CELL KILL [J].
HANSEN, MB ;
NIELSEN, SE ;
BERG, K .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 119 (02) :203-210
[10]  
KAY J, 1984, J IMMUNOL, V133, P1339