Trichosanthin inhibits antigen-specific T cell expansion through nitric oxide-mediated apoptosis pathway

被引:29
作者
Li, F
Mei, YH
Wang, Y
Chen, CH
Tu, JL
Xiao, BG
Xu, LY [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Joint Immunol Lab, Inst Hlth Sci, Shanghai 200025, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Biol Sci, Joint Immunol Lab, Shanghai Inst Immunol, Shanghai 200025, Peoples R China
[3] Shanghai Med Univ 2, Shanghai 200025, Peoples R China
[4] Fudan Univ, Neurol Inst, Shanghai, Peoples R China
基金
上海市自然科学基金;
关键词
trichosanthin; antigen-specific T lymphocytes; inducible nitric oxide synthase; nitric oxide; apoptosis;
D O I
10.1016/j.cellimm.2005.04.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trichosanthin (TCS) has been found to exhibit inflammation-suppressing effect but the underlying mechanisms are not clear. In this study, we found that TCS inhibited OVA-specific T cell proliferation in a dose-dependent manner. Such inhibition was correlated with enhanced cell death. At the same time, inducible nitric oxide synthase (iNOS) mRNA expression and protein levels were found increased in cells treated with TCS, and nitric oxide (NO) production by cells was elevated in the presence of TCS. When L-NIL, the specific inhibitor of iNOS, was added to suppress NO production induced by TCS, OVA-specific cell death was significantly inhibited, meanwhile, thymidine incorporation of cells was rescued towards normal levels. These results indicate that TCS could inhibit antigen-specific T cell activation via NO-mediated apoptosis pathway. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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