IL-2/IL-18 prevent the down-modulation of NKG2D by TGF-β in NK cells via the c-Jun N-terminal kinase (JNK) pathway

被引:46
作者
Song, Hyunkeun
Hur, Dae Young
Kim, Kyung-Eun
Park, Hyunjeong
Kim, Taesung
Kim, Chul-woo
Bang, Saic
Cho, Dae-Ho
机构
[1] Sookmyung Womens Univ, Dept Life Sci, Seoul 140742, South Korea
[2] Inje Univ, Coll Med, Dept Anat, Pusan 614735, South Korea
[3] Catholic Univ Korea, St Marys Hosp, Dept Dermatol, Seoul 150713, South Korea
[4] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
[6] Seoul Natl Univ, Coll Med, Tumor Immun Med Res Ctr, Seoul 110799, South Korea
[7] Sungkyunkwan Univ, Coll Med, Dept Plast Surg, Seoul 110745, South Korea
关键词
NK cells; NKG2D; TGF-beta; IL-2; IL-18;
D O I
10.1016/j.cellimm.2006.09.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
TGF-beta is known to play a major role for the reduced NKG2D expression seen in cancer patients. However, the mechanisms for reduced TGF-beta-induced down-regulation of NKG2D are unclear. In this study, we observed that IL-2/IL-18 increased the NKG2D expression in the TGF-beta treated NK cell line in a dose-dependent manner. Incubation with the JNK inhibitor SP600125 inhibited the NKG2D expression induced by IL-2/IL-18 in the TGF-beta treated human NK cell line. Moreover, the NK cytotoxicity assay showed that the reduced NK cytotoxicity by TGF-beta was recovered by IL-2/IL-18 treatment. The results indicate that IL-2/IL-18 strongly prevented the TGF-beta-induced NKG2D down-regulation in NK cells via the JNK pathway. Taken together, the protected expression of NKG2D by IL-2/IL-18 provides insight into the mechanism of NKG2D regulation and it also supplied useful information for creating a novel therapeutic approach to treat TGF-beta-secreting cancer cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
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