TY - JOUR
T1 - Gamma interferon-induced nitric oxide production in mouse CD5+ B1-like cell line and its association with apoptotic cell death
AU - Koide, Naoki
AU - Sugiyama, Tsuyoshi
AU - Mu, Mya Mya
AU - Mori, Isamu
AU - Yoshida, Tomoaki
AU - Hamano, Teruaki
AU - Yokochi, Takashi
PY - 2003
Y1 - 2003
N2 - The in vitro effect of gamma interferon (IFN-γ) 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-γ induced a marked NO production in TH2.52 cells through the expression of an inducible type of NO synthase (iNOS). IFN-γ 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-γ. 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-γ-induced cell death. Therefore, IFN-γ-induced NO production was possible in causing cell death in TH2.52 cells. Further, IFN-γ-induced NO production and cell death significantly were prevented by interleukin-4, a representative Th2 cytokine. The immunological significance of IFN-γ-induced NO production in a mouse B1-like cell line is discussed.
AB - The in vitro effect of gamma interferon (IFN-γ) 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-γ induced a marked NO production in TH2.52 cells through the expression of an inducible type of NO synthase (iNOS). IFN-γ 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-γ. 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-γ-induced cell death. Therefore, IFN-γ-induced NO production was possible in causing cell death in TH2.52 cells. Further, IFN-γ-induced NO production and cell death significantly were prevented by interleukin-4, a representative Th2 cytokine. The immunological significance of IFN-γ-induced NO production in a mouse B1-like cell line is discussed.
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U2 - 10.1111/j.1348-0421.2003.tb03430.x
DO - 10.1111/j.1348-0421.2003.tb03430.x
M3 - Article
C2 - 14584614
AN - SCOPUS:0141480292
SN - 0385-5600
VL - 47
SP - 669
EP - 679
JO - MICROBIOLOGY and IMMUNOLOGY
JF - MICROBIOLOGY and IMMUNOLOGY
IS - 9
ER -