Gamma interferon-induced nitric oxide production in mouse CD5+ B1-like cell line and its association with apoptotic cell death

被引:17
|
作者
Koide, N
Sugiyama, T
Mu, MM
Mori, I
Yoshida, T
Hamano, T
Yokochi, T [1 ]
机构
[1] Aichi Med Univ, Dept Microbiol & Immunol, Aichi 4801195, Japan
[2] Aichi Med Univ, Res Ctr Infect Dis, Div Bacterial Toxin, Aichi 4801195, Japan
[3] Hyogo Med Univ, Dept Med, Nishinomiya, Hyogo 6638501, Japan
关键词
IFN-gamma; B1; cell; nitric oxide; apoptosis;
D O I
10.1111/j.1348-0421.2003.tb03430.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The in vitro effect of gamma interferon (IFN-gamma) on nitric oxide (NO) production in a mouse CD5(+) B1-like cell line, TH2.52, was studied. The TH2.52 cell line is the hybridoma line between mouse B lymphoma line and mouse splenic B cells and expresses a series of B1 markers. IFN-gamma induced a marked NO production in TH2.52 cells through the expression of an inducible type of NO synthase (iNOS). IFN-gamma-induced NO production was triggered by the Janus tyrosine kinase (JAK)/signal transducer and activator of transcription (STAT) pathway since it was inhibited by AG490, a JAK2 inhibitor. The growth of TH2.52 cells significantly was inhibited in the presence of IFN-gamma. A significant number of cells underwent apoptotic cell death, accompanied by the DNA fragmentation, annexin V binding, and caspase 3 activation. N(G)-monomethyl-L-arginine, an iNOS inhibitor, prevented IFN-gamma-induced cell death. Therefore, IFN-gamma-induced NO production was possible in causing cell death in TH2.52 cells. Further, IFN-gamma-induced NO production and cell death significantly were prevented by interleukin-4, a representative Th2 cytokine. The immunological significance of IFN-gamma-induced NO production in a mouse B1-like cell line is discussed.
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页码:669 / 679
页数:11
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