The TAK1-TRAF6 signalling pathway

被引:230
作者
Landstrom, Marene [1 ]
机构
[1] Uppsala Univ, Dept Genet & Pathol, Rudbeck Lab, SE-75124 Uppsala, Sweden
基金
英国医学研究理事会;
关键词
Inflammation; Kinase activation; Transforming growth factor-beta; Ubiquitination; I-KAPPA-B; TGF-BETA; TAK1-BINDING PROTEIN-1; TAK1; ACTIVATION; TAB1; TRAF6; TRANSDUCTION; MAPKKK; FAMILY;
D O I
10.1016/j.biocel.2009.12.023
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
Cellular responses to pathogens, growth factors, cytokines, extra- or intra-cellular stress, is a prerequisite for the cell to adapt to novel and potentially dangerous situations. If the changes in the extra- or intra-cellular milieu causes DNA-damage or revoke a signalling pathway utilized during morphogenesis, the epithelial cells might be forced to undergo programmed cell death (apoptosis) in the benefit for the whole organism or transform to a mesenchymal cell type (epithelial to mesenchymal transition; EMT), in respond to a specific stimuli. An overview is presented over the current knowledge for the key components in signal transduction in homeostasis, inflammation and cancer. A handful of transcription factors are crucial for the determination of the specific cellular responses, where the transforming growth factor-beta (TGF-beta) is an important factor as discussed in this review. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:585 / 589
页数:5
相关论文
共 26 条
[1]   Ubiquitin-mediated activation of TAK1 and IKK [J].
Adhikari, A. ;
Xu, M. ;
Chen, Z. J. .
ONCOGENE, 2007, 26 (22) :3214-3226
[2]  
CHENG H, 2009, CELL SIGNAL, V2, pRA35
[3]   TAK1-binding protein 1 is a pseudophosphatase [J].
Conner, Sarah H. ;
Kular, Gursant ;
Peggie, Mark ;
Shepherd, Sharon ;
Schuttelkopf, Alexander W. ;
Cohen, Philip ;
Van Aalten, Daan M. F. .
BIOCHEMICAL JOURNAL, 2006, 399 (427-434) :427-434
[4]   Activation of the IκB kinase complex by TRAF6 requires a dimeric ubiquitin-conjugating enzyme complex and a unique polyubiquitin chain [J].
Deng, L ;
Wang, C ;
Spencer, E ;
Yang, LY ;
Braun, A ;
You, JX ;
Slaughter, C ;
Pickart, C ;
Chen, ZJ .
CELL, 2000, 103 (02) :351-361
[5]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584
[6]  
HELDIN CH, 2009, CURRENT OPINION CELL, V21, P1
[7]   The age of crosstalk: Phosphorylation, ubiquitination, and beyond [J].
Hunter, Tony .
MOLECULAR CELL, 2007, 28 (05) :730-738
[8]   TAK1-binding Protein 1, TAB1, Mediates Osmotic Stress-induced TAK1 Activation but Is Dispensable for TAK1-mediated Cytokine Signaling [J].
Inagaki, Maiko ;
Omori, Emily ;
Kim, Jae-Young ;
Komatsu, Yoshihiro ;
Scott, Greg ;
Ray, Manas K. ;
Yamada, Gen ;
Matsumoto, Kunihiro ;
Mishina, Yuji ;
Ninomiya-Tsuji, Jun .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (48) :33080-33086
[9]   Targeted disruption of the Tab1 gene causes embryonic lethality and defects in cardiovascular and lung morphogenesis [J].
Komatsu, Y ;
Shibuya, H ;
Takeda, N ;
Ninomiya-Tsuji, J ;
Yasui, T ;
Miyado, K ;
Sekimoto, T ;
Ueno, N ;
Matsumoto, K ;
Yamada, G .
MECHANISMS OF DEVELOPMENT, 2002, 119 (02) :239-249
[10]   Deletion of a small consensus region at 6q15, including the MAP3K7 gene, is significantly associated with high-grade prostate cancers [J].
Liu, Wennuan ;
Chang, Bao-Li ;
Cramer, Scott ;
Koty, Patrick P. ;
Li, Tao ;
Sun, Jishan ;
Turner, Aubrey R. ;
Kap-Herr, ChrisVon ;
Bobb, Peggy ;
Rao, Jianyu ;
Zheng, S. Lilly ;
Isaacs, William B. ;
Xu, Jianfeng .
CLINICAL CANCER RESEARCH, 2007, 13 (17) :5028-5033