IL-18 enhances SCF production of melanoma cells by regulating ROI and p38 MAPK activity

被引:22
作者
Hue, J
Kim, A
Song, H
Choi, I
Park, H
Kim, T
Lee, WJ
Kang, H
Cho, D
机构
[1] Sookmyung Womens Univ, Dept Life Sci, Seoul, South Korea
[2] Sookmyung Womens Univ, Coll Pharm, Seoul, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Immunol Lab, Seoul, South Korea
[4] Catholic Univ, Dept Dermatol, St Marys Hosp, Seoul, South Korea
[5] Chonnam Natl Univ, Coll Pharm, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Anat & Tumor Immunity, Med Res Ctr, Seoul, South Korea
[7] Chonnam Natl Univ, Sch Biol Sci & Technol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
IL-18; SCF melanoma; ROI; p38; MAPK;
D O I
10.1016/j.imlet.2004.08.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been reported that interleukin-18 (IL-18) is secreted by B16 murine melanoma cells and that this endogenous IL-18 is involved in the immune escape of murine melanoma cells. The present study investigated whether interleukin (IL)-18 can regulate stem cell factor (SCF) expression, known to be associated with melanocyte proliferation, in B16F10 murine melanoma cells. SCF expression was examined by RT-PCR, intracellular FACS analysis, and ELISA in IL-18 antisense transfectants. Transfection with IL-18 antisense cDNA reduced SCF expression and the expression was enhanced by addition of exogenous IL-18. In addition, the effect of IL-18 was blocked by the antioxidant, N-acetyl-L-cysteine (NAC), indicating that IL-18 regulates ROI production, which is involved in SCF production. Furthermore, inhibitors of p38 mitogen-activated protein kinase (MAPK), such as SB203580, blocked enhanced SCF expression, indicating that p38 MAPK activity is required for IL-18-enhanced SCF production. Taken together, these results suggest that IL-18 plays a critical role as a regulatory factor of SCF expression via ROI and p38 MAPK activity in B16F10 murine melanoma cells. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 217
页数:7
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