Transcriptional and posttranscriptional regulation of the plasminogen activator system

被引:67
作者
Nagamine, Y
Medcalf, RL
Muñoz-Cánoves, P
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[2] Monash Univ, Dept Med, Australian Ctr Blood Dis, AMREP, Prahran, Vic, Australia
[3] CRG, Programa Diferenciacio & Canc, Barcelona, Spain
关键词
review; plasminogen activator; gene regulation; mRNA stability;
D O I
10.1160/TH04-12-0814
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The core protein components of the plasminogen activator (PA) system are two plasminogen activators, two plasminogen activator inhibitors and a urokinase type plasminogen activator-specific cell surface receptor. Various types of biological regulation are exerted through the interplay of these components mutually and with extracellular matrix proteins and cell membrane proteins, with or without involving proteolytic activity. Reflecting these diverse biological roles, the level and activity of each component of the PA system is under the control of a variety of regulatory mechanisms. The expression level of a protein reflects the level of the corresponding mRNA, which is essentially the net result of de novo, synthesis, i.e. transcription, and degradation. Many recent studies have shown that the regulation of mRNA stability is dynamic and cell specific. Accordingly, we are learning that the mRNAs of the PA system are also the subject of diverse regulatory mechanisms. In this short review, we summarize current understanding of the transcriptional and mRNA-stability regulation of the PA system.
引用
收藏
页码:661 / 675
页数:15
相关论文
共 269 条
[31]   A CELL-TYPE SPECIFIC AND ENHANCER-DEPENDENT SILENCER IN THE REGULATION OF THE EXPRESSION OF THE HUMAN UROKINASE PLASMINOGEN-ACTIVATOR GENE [J].
CANNIO, R ;
RENNIE, PS ;
BLASI, F .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2303-2308
[32]   IDENTIFICATION OF A COMMON NUCLEOTIDE-SEQUENCE IN THE 3'-UNTRANSLATED REGION OF MESSENGER-RNA MOLECULES SPECIFYING INFLAMMATORY MEDIATORS [J].
CAPUT, D ;
BEUTLER, B ;
HARTOG, K ;
THAYER, R ;
BROWNSHIMER, S ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1670-1674
[33]   Feedback inhibition of macrophage tumor necrosis factor-α production by tristetraprolin [J].
Carballo, E ;
Lai, WS ;
Blackshear, PJ .
SCIENCE, 1998, 281 (5379) :1001-1005
[34]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[35]  
Chapman HA, 2001, THROMB HAEMOSTASIS, V86, P124
[36]  
CHEN CS, 1993, J CELL SCI, V106, P45
[37]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[38]   MEK1,2 response element mediates angiotensin II-stimulated plasminogen activator inhibitor-1 promoter activation [J].
Chen, HC ;
Feener, EP .
BLOOD, 2004, 103 (07) :2636-2644
[39]   αv integrin, p38 mitogen-activated protein kinase, and urokinase plasminogen activator are functionally linked in invasive breast cancer cells. [J].
Chen, J ;
Baskerville, C ;
Han, QW ;
Pan, ZXK ;
Huang, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :47901-47905
[40]   Identification and localization of a fatty acid response region in the human plasminogen activator inhibitor-1 gene [J].
Chen, YB ;
Billadello, JJ ;
Schneider, DJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (12) :2696-2701