TWEAK, a member of the TNF superfamily, is a multifunctional cytokine that binds the TweakR/Fn14 receptor

被引:249
作者
Wiley, SR [1 ]
Winkles, JA
机构
[1] Amgen Corp, Seattle, WA 98101 USA
[2] Amer Red Cross, Jerome H Holland Lab Biomed Sci, Vasc Biol Dept, Rockville, MD 20855 USA
[3] George Washington Univ, Med Ctr, Inst Biomed Sci, Dept Biochem & Mol Biol, Washington, DC 20037 USA
关键词
TWEAK; TweakR; Fn14; TNF; TRAF;
D O I
10.1016/S1359-6101(03)00019-4
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
The cytokine tumor necrosis factor-like weak inducer of apoptosis (TWEAK) was initially described as a member of the tumor necrosis factor (TNF) superfamily in 1997. TWEAK is a cell surface-associated type 11 transmembrane protein, but a smaller, biologically active form can also be shed into the extracellular milieu. There is one receptor currently known to bind TWEAK with physiological affinity, and it is a type I transmembrane protein that is referred to in the literature as either TWEAK receptor (TweakR) or fibroblast growth factor-inducible 14 (1704). TweakR/Fn14 is the smallest member of the TNF receptor (TNFR) superfamily described to date, and it appears to signal via recruitment of several different TNFR-associated factors. TWEAK has multiple biological activities, including stimulation of cell growth and angiogenesis, induction of inflammatory cytokines, and under some experimental conditions, stimulation of apoptosis. In this report, we summarize the results from recent studies focused on the TWEAK cytokine. Although these studies have contributed a significant amount of new information, numerous questions still remain regarding the role of TWEAK in both normal physiology and the pathogenesis of human disease. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:241 / 249
页数:9
相关论文
共 46 条
[11]   Down-regulated expression of TWEAK mRNA in acute and chronic inflammatory pathologies [J].
Chicheportiche, Y ;
Fossati-Jimack, L ;
Moll, S ;
Ibnou-Zekri, N ;
Izui, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 279 (01) :162-165
[12]   The Fn14 immediate-early response gene is induced during liver regeneration and highly expressed in both human and murine hepatocellular carcinomas [J].
Feng, SLY ;
Guo, Y ;
Factor, VM ;
Thorgeirsson, SS ;
Bell, DW ;
Testa, JR ;
Peifley, KA ;
Winkles, JA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (04) :1253-1261
[13]  
Han HY, 2002, CANCER RES, V62, P2890
[14]   Tumor necrosis factor receptor-associated factor (TRAF) family: Adapter proteins that mediate cytokine signaling [J].
Inoue, J ;
Ishida, T ;
Tsukamoto, N ;
Kobayashi, N ;
Naito, A ;
Azuma, S ;
Yamamoto, T .
EXPERIMENTAL CELL RESEARCH, 2000, 254 (01) :14-24
[15]  
Jakubowski A, 2002, J CELL SCI, V115, P267
[16]   TRAIL (Apo2 ligand) and TWEAK (Apo3 ligand) mediate CD4+ T cell killing of antigen-presenting macrophages [J].
Kaplan, MJ ;
Ray, D ;
Mo, RR ;
Yung, RL ;
Richardson, BC .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :2897-2904
[17]   The apoptotic ligands TRAIL, TWEAK, and Fas ligand mediate monocyte death induced by autologous lupus T cells [J].
Kaplan, MJ ;
Lewis, EE ;
Shelden, EA ;
Somers, E ;
Pavlic, R ;
McCune, WJ ;
Richardson, BC .
JOURNAL OF IMMUNOLOGY, 2002, 169 (10) :6020-6029
[18]   Studies on the interaction between TWEAK and the death receptor WSL-1/TRAMP (DR3) [J].
Kaptein, A ;
Jansen, M ;
Dilaver, G ;
Kitson, J ;
Dash, L ;
Wang, E ;
Owen, MJ ;
Bodmer, JL ;
Tschopp, J ;
Farrow, SN .
FEBS LETTERS, 2000, 485 (2-3) :135-141
[19]   Fibroblasts in mechanically stressed collagen lattices assume a "synthetic" phenotype [J].
Kessler, D ;
Dethlefsen, S ;
Haase, I ;
Plomann, M ;
Hirche, F ;
Krieg, T ;
Eckes, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36575-36585
[20]   The TNF and TNF receptor superfamilies: Integrating mammalian biology [J].
Locksley, RM ;
Killeen, N ;
Lenardo, MJ .
CELL, 2001, 104 (04) :487-501