Induction of RANTES by TWEAK/Fn14 interaction in human keratinocytes

被引:62
|
作者
Jin, L
Nakao, A
Nakayama, M
Yamaguchi, N
Kojima, Y
Nakano, N
Tsuboi, R
Okumura, K
Yagita, H
Ogawa, H
机构
[1] Univ Yamanashi, Fac Med, Dept Immunol, Yamanashi 4093898, Japan
[2] Juntendo Univ, Sch Med, Atopy Allergy Res Ctr, Tokyo 113, Japan
[3] Tokyo Med Univ, Dept Dermatol, Tokyo, Japan
[4] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 113, Japan
[5] Juntendo Univ, Sch Med, Dept Dermatol, Tokyo 113, Japan
[6] Juntendo Univ, Sch Med, Div Pathol, Cent Lab Med Sci, Tokyo 113, Japan
关键词
keratinocytes; RANTES; TGF-beta; TWEAK;
D O I
10.1111/j.0022-202X.2004.22419.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
TNF-like weak inducer of apoptosis (TWEAK), a member of the tumor necrosis factor (TNF) family, is a multifunctional cytokine that regulate cellular proliferation, angiogenesis, inflammation, and apoptosis. In this study, we investigated the effect of TWEAK on human keratinocytes. Primary cultured normal human keratinocytes constitutively expressed a TWEAK receptor, fibroblast growth factor-inducible 14 (Fn14), and produced regulated on activation, normal T expressed and secreted (RANTES) upon TWEAK stimulation in a concentration-dependent manner. The TWEAK-induced RANTES production was abrogated by anti-Fn14 antibody, and synergistically augmented by simultaneous stimulation with transforming growth factor-beta. In addition, human keratinocytes differentiated in vitro with high Ca2+-containing medium showed enhanced production of RANTES upon TWEAK stimulation. Furthermore, TWEAK induced rapid phosphorylation of IkappaB-alpha in human keratinocytes. Collectively, TWEAK acts on human keratinocytes as an inducer of RANTES via Fn14. Because RANTES has been implicated in inflammation, TWEAK/Fn14 interaction in human keratinocytes may be involved in the pathophysiology of inflammatory skin disorders.
引用
收藏
页码:1175 / 1179
页数:5
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