Differential effects of N-acetyl-L-cysteine on IL-2-vs IL-12-driven proliferation of a T cell clone: Implications for distinct signalling pathways

被引:4
作者
Park, CS
Park, WR
Sugimoto, N
Nakahira, M
Ahn, HJ
Hamaoka, T
Ohta, T
Kurimoto, M
Fujiwara, H
机构
[1] Osaka Univ, Grad Sch Med, Biomed Res Ctr, Dept Oncol, Suita, Osaka 5650871, Japan
[2] Fujisaki Inst, Hayashibara Biochem Labs, Okayama, Japan
关键词
N-acetylcysteine; T cell proliferation; signal transduction; interleukin 2 (IL-2); interleukin 12 (IL-12);
D O I
10.1006/cyto.2000.0722
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
Using a T cell clone (2D6) capable of responding to IL-2 and IL-12, we compared the effects of NAC on IL-2 and IL-12-driven T cell proliferation. Addition of N-acetylcysteine (NAC) to 2D6 cultures did not affect IL-2 stimulated proliferation, but strikingly inhibited IL-12 stimulated proliferation. These differential NAC effects did not correlate with the patterns of the mitogen-activated protein kinase (MAPK) activation following cytokine stimulation and its regulation by NAC, Although a p38 MAPK inhibitor downregulated both IL-2- and IL-12-induced proliferation, this effect was seen at drug concentrations one order higher than those reportedly used to specifically inhibit p38 MAPK. The results suggest the existence of distinct signalling pathways and a common, indispensable signalling molecule in IL-2- and IL-12 driven T cell proliferation. (C) 2000 Academic Press.
引用
收藏
页码:1419 / 1422
页数:4
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