ADAM-17: the enzyme that does it all

被引:327
作者
Gooz, Monika [1 ]
机构
[1] Med Univ S Carolina, Dept Med, Div Nephrol, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
Ectodomain shedding; growth factor; inflammation; signalling; proteolysis; TNF alpha; TUMOR-NECROSIS-FACTOR; ALPHA-CONVERTING-ENZYME; GROWTH-FACTOR RECEPTOR; AMYLOID-PRECURSOR-PROTEIN; SNAKE-VENOM DISINTEGRIN; POLYCYSTIC KIDNEY-DISEASE; ECTODOMAIN SHEDDING ACTIVITY; ACUTE MYOCARDIAL-INFARCTION; OXYGEN-GLUCOSE DEPRIVATION; MESSENGER-RNA EXPRESSION;
D O I
10.3109/10409231003628015
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
This review focuses on the role of ADAM-17 in disease. Since its debut as the tumor necrosis factor converting enzyme (TACE), ADAM-17 has been reported to be an indispensible regulator of almost every cellular event from proliferation to migration. The central role of ADAM-17 in cell regulation is rooted in its diverse array of substrates: cytokines, growth factors, and their receptors as well as adhesion molecules are activated or inactivated by their cleavage with ADAM-17. It is therefore not surprising that ADAM-17 is implicated in numerous human diseases including cancer, heart disease, diabetes, rheumatoid arthritis, kidney fibrosis, Alzheimer's disease, and is a promising target for future treatments. The specific role of ADAM-17 in the pathophysiology of these diseases is very complex and depends on the cellular context. To exploit the therapeutic potential of ADAM-17, it is important to understand how its activity is regulated and how specific organs and cells can be targeted to inactivate or activate the enzyme.</.
引用
收藏
页码:146 / 169
页数:24
相关论文
共 294 条
[1]   Selenium supplementation induces metalloproteinase-dependent L-selectin shedding from monocytes [J].
Ahrens, Ingo ;
Ellwanger, Christoph ;
Smith, Belinda K. ;
Bassler, Nicole ;
Chen, Yung Chih ;
Neudorfer, Irene ;
Ludwig, Andreas ;
Bode, Christoph ;
Peter, Karlheinz .
JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 83 (06) :1388-1395
[2]   ADAMs family members as amyloid precursor protein α-secretases [J].
Allinson, TMJ ;
Parkin, ET ;
Turner, AJ ;
Hooper, NM .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (03) :342-352
[3]   Regulation of tumor necrosis factor-α and tumor necrosis factor converting enzyme in human osteoarthritis [J].
Amin, AR .
OSTEOARTHRITIS AND CARTILAGE, 1999, 7 (04) :392-394
[4]   TNF-α converting enzyme (TACE) is inhibited by TIMP-3 [J].
Amour, A ;
Slocombe, PM ;
Webster, A ;
Butler, M ;
Knight, CG ;
Smith, BJ ;
Stephens, PE ;
Shelley, C ;
Hutton, M ;
Knäuper, V ;
Docherty, AJP ;
Murphy, G .
FEBS LETTERS, 1998, 435 (01) :39-44
[5]  
ANDERSON JP, 1992, J NEUROCHEM, V59, P2328
[6]   ADAMs, cell migration and cancer [J].
Arribas, J ;
Bech-Serra, JJ ;
Santiago-Josefat, B .
CANCER AND METASTASIS REVIEWS, 2006, 25 (01) :57-68
[7]   Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo [J].
Atreya, R ;
Mudter, J ;
Finotto, S ;
Müllberg, J ;
Jostock, T ;
Wirtz, S ;
Schütz, M ;
Bartsch, B ;
Holtmann, M ;
Becker, C ;
Strand, D ;
Czaja, J ;
Schlaak, JF ;
Lehr, HA ;
Autschbach, F ;
Schürmann, G ;
Nishimoto, N ;
Yoshizaki, K ;
Ito, H ;
Kishimoto, T ;
Galle, PR ;
Rose-John, S ;
Neurath, MF .
NATURE MEDICINE, 2000, 6 (05) :583-588
[8]   Timp-3 deficiency impairs cognitive function in mice [J].
Baba, Yoshichika ;
Yasuda, Osamu ;
Takemura, Yukihiro ;
Ishikawa, Yasuyuki ;
Ohishi, Mitsuru ;
Iwanami, Jun ;
Mogi, Masaki ;
Doe, Nobutaka ;
Horiuchi, Masatsugu ;
Maeda, Nobuyo ;
Fukuo, Keisuke ;
Rakugi, Hiromi .
LABORATORY INVESTIGATION, 2009, 89 (12) :1340-1347
[9]   Role of the APP non-amyloidogenic signaling pathway and targeting α-secretase as an alternative drug target for treatment of Alzheimer's disease [J].
Bandyopadhyay, S. ;
Goldstein, L. E. ;
Lahiri, D. K. ;
Rogers, J. T. .
CURRENT MEDICINAL CHEMISTRY, 2007, 14 (27) :2848-2864
[10]   Back signaling by the Nrg-1 intracellular domain [J].
Bao, JX ;
Wolpowitz, D ;
Role, LW ;
Talmage, DA .
JOURNAL OF CELL BIOLOGY, 2003, 161 (06) :1133-1141