Metabolic, hormonal and environmental regulation of plasminogen activator inhibitor-1 (PAI-1) expression: Lessons from the liver

被引:69
作者
Dimova, ElitsaY. [1 ]
Kietzmann, Thomas [1 ]
机构
[1] Univ Kaiserslautern, Dept Chem Biochem, D-67663 Kaiserslautern, Germany
关键词
Fibrinolysis inhibitors; gene expression; plasminogen activator inhibitors; transcription factors; hypoxia;
D O I
10.1160/TH08-07-0490
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Plasminogen activator inhibitor-1 (PAI-1) controls the regulation of the fibrinolytic system in blood by inhibiting both urokinase-type and tissue-type plasminogen activators. Enhanced levels of PAI-1 are found in patients with type 2 diabetes mellitus which is associated with a dysbalance in glucose and lipid homeostasis. Especially a defective insulin response in the liver contributes to the development of hyperglycemia, dyslipidemia and peripheral insulin resistance and may contribute to hepatic overexpression of PAI-1 in diabetes type 2. Furthermore, a substantial upregulation of PAI-1 expression has also been shown in a variety of liver injury models. Thus, the liver appears to be not only a major site of PAI-1 synthesis in response to hormonal changes, but also in response to a variety of other pathological events. PAI-1 expression in liver largely depends on activation of signalling pathways and transcriptional regulators which may be the basis for a new level of cross-talk between different signalling pathways and thus may represent attractive therapeutic candidates. This article will primarily focus on the regulation of PAI-1 expression in liver cells and discuss potential cross-talks between metabolic, hormonal and environmental signals.
引用
收藏
页码:992 / 1006
页数:15
相关论文
共 185 条
[11]   Hypoxia up-regulates hypoxia-inducible factor-1α transcription by involving phosphatidylinositol 3-kinase and nuclear factor κB in pulmonary artery smooth muscle cells [J].
BelAiba, Rachida S. ;
Bonello, Steve ;
Zaehringer, Christian ;
Schmidt, Stefanie ;
Hess, John ;
Kietzmann, Thomas ;
Goerlach, Agnes .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (12) :4691-4697
[12]   Critical role of plasminogen activator inhibitor-1 in cholestatic liver injury and fibrosis [J].
Bergheim, I ;
Guo, LP ;
Davis, MA ;
Duveau, I ;
Arteel, GE .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 316 (02) :592-600
[13]   Metformin prevents alcohol-induced liver injury in the mouse: Critical role of plasminogen activator inhibitor-1 [J].
Bergheim, Ina ;
Guo, Luping ;
Davis, Molly Anne ;
Lambert, Jason C. ;
Beier, Juliane I. ;
Duveau, Ilinca ;
Luyendyk, James P. ;
Roth, Robert A. ;
Arteel, Gavin E. .
GASTROENTEROLOGY, 2006, 130 (07) :2099-2112
[14]   Protein kinase B/Akt-mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1 [J].
Biggs, WH ;
Meisenhelder, J ;
Hunter, T ;
Cavenee, WK ;
Arden, KC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7421-7426
[15]   The MET oncogene drives a genetic programme linking cancer to haemostasis [J].
Boccaccio, C ;
Sabatino, G ;
Medico, E ;
Girolami, F ;
Follenzi, A ;
Reato, G ;
Sottile, A ;
Naldini, L ;
Comoglio, PM .
NATURE, 2005, 434 (7031) :396-400
[16]   Reactive oxygen species activate the HIF-1α promoter via a functional NFκB site [J].
Bonello, Steve ;
Zahringer, Christian ;
BelAiba, Rachida S. ;
Djordjevic, Talija ;
Hess, John ;
Michiels, Carine ;
Kietzmann, Thomas ;
Goerlach, Agnes .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (04) :755-761
[17]  
BOSMA PJ, 1988, J BIOL CHEM, V263, P9129
[18]   Vitamin C inhibits NF-κB activation by TNF via the activation of p38 mitogen-activated protein kinase [J].
Bowie, AG ;
O'Neill, LAJ .
JOURNAL OF IMMUNOLOGY, 2000, 165 (12) :7180-7188
[19]   Modulation of angiotensin II and norepinephrine-induced plasminogen activator inhibitor-1 expression by AT1a receptor deficiency [J].
Brown, N. J. ;
Bradford, J. ;
Wang, Z. ;
Lea, W. ;
Ma, L. ;
Ma, J. ;
Vaughan, D. E. ;
Fogo, A. B. .
KIDNEY INTERNATIONAL, 2007, 72 (01) :72-81
[20]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820