Innate resistance to experimental African trypanosomiasis:: Differences in cytokine (TNF-α, IL-6, IL-10 and IL-12) production by bone marrow-derived macrophages from resistant and susceptible mice

被引:50
作者
Kaushik, RS [1 ]
Uzonna, JE [1 ]
Zhang, Y [1 ]
Gordon, JR [1 ]
Tabel, H [1 ]
机构
[1] Univ Saskatchewan, Western Coll Vet Med, Dept Vet Microbiol, Saskatoon, SK S7N 5B4, Canada
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
cytokines; macrophage; resistance; Trypanosoma;
D O I
10.1006/cyto.2000.0685
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
Resistance to African trypanosomiasis is under multigenic control. BaLB/c mice are highly susceptible while C57Bl/6 mice are relatively resistant. Macrophages eliminate opsonized trypanosomes from the bloodstream and are involved in immunosuppression. We therefore investigated the production of a number of cytokines (IL-10, IL-6, TNF-alpha and IL-12) by bone marrow-derived macrophages (BMDM) from C57Bl/6 and BALB/c mice following challenge with either Trypanosoma congolense or Trypanosoma brucei. BMDM from C57BI/6 mice, upon challenge with whole cell extracts (WCE) of T. congolense or T. brucei, produced significantly more TNF-alpha and IL-12 than those from BALB/c mice, The production of these cytokines was significantly enhanced by pretreatment of the cells with IFN-gamma, BMDM from BALB/c mice, however, produced significantly more IL-6 and IL-10 than those from C57Bl/6 mice. In contrast to LPS stimulation, simultaneous treatment of cells with WCE and IFN-gamma enhanced IL-10 synthesis by BMDM from BALB/c mice. These results indicate that cytokine genes are differentially regulated in macrophages from trypanosome-susceptible and -resistant mice and are consistent with our previous findings wherein retrovirus-immortalized macrophage cell lines from BALB/c and C57Bl/6 mice produce differential amounts of cytokines after phagocytosis of trypanosomes. (C) 1000 Academic Press.
引用
收藏
页码:1024 / 1034
页数:11
相关论文
共 59 条
[1]  
ASKONAS BA, 1985, CURR TOP MICROBIOL, V117, P119
[2]   THE BIOLOGY OF CACHECTIN/TNF - A PRIMARY MEDIATOR OF THE HOST RESPONSE [J].
BEUTLER, B ;
CERAMI, A .
ANNUAL REVIEW OF IMMUNOLOGY, 1989, 7 :625-655
[3]  
BLACKETT A, 1983, INT J CLIN PHARM RES, V3, P5
[4]  
Clayton C E, 1979, Parasite Immunol, V1, P241, DOI 10.1111/j.1365-3024.1979.tb00709.x
[5]   GENETICS OF RESISTANCE TO THE AFRICAN TRYPANOSOMES .4. RESISTANCE OF RADIATION CHIMERAS TO TRYPANOSOMA-RHODESIENSE INFECTION [J].
DEGEE, ALW ;
MANSFIELD, JM .
CELLULAR IMMUNOLOGY, 1984, 87 (01) :85-91
[6]  
DEMPSEY WL, 1983, J IMMUNOL, V130, P405
[7]  
DESCOTEAUX A, 1990, J IMMUNOL, V145, P846
[8]  
DESCOTEAUX A, 1992, J IMMUNOL, V149, P3008
[9]  
FIORENTINO DF, 1991, J IMMUNOL, V147, P3815
[10]  
FORTIER AH, 1994, CURR PROT IMMUNOL