Mycoplasma arginini enhances cytotoxicity of thioglycollate-elicited murine macrophages toward YAC-1 tumor cells through production of NO

被引:20
作者
Ribeiro-Dias, F
Russo, M
Barbuto, JAM
do Nascimento, FRF
Timenetsky, J
Jancar, S
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05580900 Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Microbiol, BR-05580900 Sao Paulo, Brazil
关键词
cytotoxicity; prostaglandin E-2;
D O I
10.1002/jlb.65.6.808
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bacterial products stimulate macrophage tumoricidal activity through release of tumor necrosis factor (TNF) and nitric oxide (NO). We show here that thioglycollate-elicited macrophages acquire cytotoxic activity when cocultured with Mycoplasma arginini-infected YAC-1 tumor cells and release TNF and NO. Fixed mycoplasma-infected cells, supernatants from infected-cell cultures, or purified heat-killed mycoplasma obtained from cell-free cultures were all able to induce TNF and NO production. Thus, the mycoplasma per se and not a product of infected cells induce the release of these molecules. Addition of prostaglandin E-2 (PGE(2)) to the cocultures, which reduced TNF release, or antibodies to TNF, did not affect macrophage cytotoxicity nor NO release. Inhibition of NO production by L-NAME or aminoguanidine reduced the cytotoxicity, and treatment with a NO donor was toxic to YAC-1 cells, These results indicate that M. arginini activates thioglycollate-elicited murine macrophages for NO and TNF release increasing their cytotoxic activity toward YAC-1 cells and that this activity is dependent on NO but not TNF release.
引用
收藏
页码:808 / 814
页数:7
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