|
Elitsa Y. Dimova; Thomas Kietzmann
Department of Chemistry/Biochemistry, University of Kaiserslautern, Kaiserslautern, Germany
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.
Hypoxia, gene expression, Plasminogen activator inhibitors, transcription factors, fibrinolysis inhibitors
| 1. | ||
Rashna D. Balsara; Victoria A. Ploplis Thrombosis and Haemostasis 2008 100 6: 1029-1036 http://dx.doi.org/10.1160/TH08-07-0427 | ||
| 2. | ||
María González-Díez, Cristina Rodríguez, Lina Badimon, José Martínez-González Thrombosis and Haemostasis 2008 100 1: 119-126 http://dx.doi.org/10.1160/TH07-11-0675 | ||
| 3. | ||
Sanjiv Baxi1, David L. Crandall3, Thomas R. Meier*,1,2, Shirley Wrobleski1, Angela Hawley1, Diana Farris1, Hassan Elokdah4†, Robert Sigler5, Robert G. Schaub**, 3, Thomas Wakefield1, Daniel Myers1, 2 Thrombosis and Haemostasis 2008 99 4: 749-758 http://dx.doi.org/10.1160/TH07-11-0669 | ||