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
  • [1] Transcription factor decoy for activator protein-1 (AP-1) inhibits high glucose- and angiotensin II-induced type 1 plasminogen activator inhibitor (PAI-1) gene expression in cultured human vascular smooth muscle cells
    Ahn, JD
    Morishita, R
    Kaneda, Y
    Lee, KU
    Park, JY
    Jeon, YJ
    Song, HS
    Lee, IK
    [J]. DIABETOLOGIA, 2001, 44 (06) : 713 - 720
  • [2] Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha
    Alessi, DR
    James, SR
    Downes, CP
    Holmes, AB
    Gaffney, PRJ
    Reese, CB
    Cohen, P
    [J]. CURRENT BIOLOGY, 1997, 7 (04) : 261 - 269
  • [3] Production of plasminogen activator inhibitor 1 by human adipose tissue - Possible link between visceral fat accumulation and vascular disease
    Alessi, MC
    Peiretti, F
    Morange, P
    Henry, M
    Nalbone, G
    JuhanVague, I
    [J]. DIABETES, 1997, 46 (05) : 860 - 867
  • [4] GROWTH FACTOR-ACTIVATED KINASES PHOSPHORYLATE IRE-ABP
    ALEXANDERBRIDGES, M
    MUKHOPADHYAY, NK
    JHALA, U
    DENARO, M
    KONG, XF
    AVRUCH, J
    MALLER, J
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1992, 20 (03) : 691 - 693
  • [5] Upstream stimulatory factor regulates E box-dependent PAI-1 transcription in human epidermal keratinocytes
    Allen, RR
    Qi, L
    Higgins, PJ
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 203 (01) : 156 - 165
  • [6] PLASMINOGEN-ACTIVATOR INHIBITOR TYPE-1 - REACTIVE CENTER AND AMINO-TERMINAL HETEROGENEITY DETERMINED BY PROTEIN AND CDNA SEQUENCING
    ANDREASEN, PA
    RICCIO, A
    WELINDER, KG
    DOUGLAS, R
    SARTORIO, R
    NIELSEN, LS
    OPPENHEIMER, C
    BLASI, F
    DANO, K
    [J]. FEBS LETTERS, 1986, 209 (02) : 213 - 218
  • [7] Role of c-Jun and proximal phorbol 12-myristate-13-acetate-(PMA)-responsive elements in the regulation of basal and PMA-stimulated plasminogen-activator inhibitor-1 gene expression in HepG2
    Arts, J
    Grimbergen, J
    Bosma, PJ
    Rahmsdorf, HJ
    Kooistra, T
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 241 (02): : 393 - 402
  • [8] Transcriptional regulation of plasminogen activator inhibitor type I gene by insulin - Insights into the signaling pathway
    Banfi, C
    Eriksson, P
    Giandomenico, G
    Mussoni, L
    Sironi, L
    Hamsten, A
    Tremoli, E
    [J]. DIABETES, 2001, 50 (07) : 1522 - 1530
  • [9] ZONAL REDOX CHANGES AS A CAUSE OF SELECTIVE PERIVENULAR HEPATOTOXICITY OF ALCOHOL
    BARAONA, E
    JAUHONEN, P
    MIYAKAWA, H
    LIEBER, CS
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1983, 18 : 449 - 454
  • [10] Liver fibrogenesis:: A new role for the renin-angiotensin system
    Bataller, R
    Sancho-Bru, P
    Ginès, P
    Brenner, DA
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2005, 7 (9-10) : 1346 - 1355