Literature DB >> 21052830

Atorvastatin neutralises the thrombin-induced tissue factor expresion in endothelial cells via geranylgeranyl pyrophosphate.

Vicenta Martínez-Sales1, Virtudes Vila, Marcos Ferrando, Edelmiro Reganon.   

Abstract

Statins may have beneficial effects in atherogenesis given their antithrombotic properties involving non-lipid mechanisms that modify endothelial function of tissue factor induction by thrombin. In this study, we investigate the effect of atorvastatin on tissue factor (TF) activity in thrombin-stimulated endothelial cells and its regulation through mevalonate or its derivatives. First subculture of human umbilical endothelial cells was used for this study. Cells were treated with thrombin and atorvastatin for different time intervals and dosage. Tissue factor activity was measured as Factor Xa generation induced by Tissue Factor-Factor VIIa complex on confluent cells. Our results show that atorvastatin prevents the thrombin-induced up-regulation of tissue factor activity in a concentration-dependent manner. Mevalonate and geranylgeranyl pyrophosphate reversed this inhibitory effect of atorvastatin on tissue factor activity, while the presence of farnesyl pyrophosphate did not prevent the atorvastatin effect on thrombin-induced tissue factor activity. Rho-kinase inhibitor did not affect the thrombin stimulation of tissue factor activity. High amount of hydrophobic isoprenoid groups decreases the thrombin-induced TF activity and may promote endothelial cell anti-thrombotic action. Rho kinase pathways do not have a major role in the thrombin-mediated TF activity. The inhibitory effect of atorvastatin on thrombin-induced TF activity was partially reversed by MVA and GGPP but not FPP.

Entities:  

Year:  2010        PMID: 21052830      PMCID: PMC3021141          DOI: 10.1007/s10616-010-9319-4

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  13 in total

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2.  Inhibition of tissue-factor-mediated thrombin generation by simvastatin.

Authors:  D Ferro; S Basili; C Alessandri; D Cara; F Violi
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4.  Multiple-dose pharmacokinetics, pharmacodynamics, and safety of atorvastatin, an inhibitor of HMG-CoA reductase, in healthy subjects.

Authors:  D D Cilla; L R Whitfield; D M Gibson; A J Sedman; E L Posvar
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5.  Statin prevents tissue factor expression in human endothelial cells: role of Rho/Rho-kinase and Akt pathways.

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6.  Thrombin-induced rapid geranylgeranylation of RhoA as an essential process for RhoA activation in endothelial cells.

Authors:  Hiroshi Ohkawara; Toshiyuki Ishibashi; Takayuki Sakamoto; Koichi Sugimoto; Kenji Nagata; Keiko Yokoyama; Nobuo Sakamoto; Masashi Kamioka; Isao Matsuoka; Shigetomo Fukuhara; Naotoshi Sugimoto; Yoh Takuwa; Yukio Maruyama
Journal:  J Biol Chem       Date:  2005-01-07       Impact factor: 5.157

7.  HMG CoA reductase inhibitor suppresses the expression of tissue factor and plasminogen activator inhibitor-1 induced by angiotensin II in cultured rat aortic endothelial cells.

Authors:  Yasufumi Kunieda; Katsumi Nakagawa; Hiromi Nishimura; Hisato Kato; Naoki Ukimura; Shingo Yano; Hidehiko Kawano; Shinzo Kimura; Masao Nakagawa; Hajime Tsuji
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8.  3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors interfere with angiogenesis by inhibiting the geranylgeranylation of RhoA.

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9.  Atorvastatin neutralizes the up-regulation of thrombospondin-1 induced by thrombin in human umbilical vein endothelial cells.

Authors:  Vicenta Martínez-Sales; Virtudes Vila; Marcos Ferrando; Edelmiro Reganon
Journal:  Endothelium       Date:  2007 Jul-Oct

10.  Integral role of RhoA activation in monocyte adhesion-triggered tissue factor expression in endothelial cells.

Authors:  Toshiyuki Ishibashi; Takayuki Sakamoto; Hiroshi Ohkawara; Kenji Nagata; Koichi Sugimoto; Sotaro Sakurada; Naotoshi Sugimoto; Atai Watanabe; Keiko Yokoyama; Nobuo Sakamoto; Masahiko Kurabayashi; Yoh Takuwa; Yukio Maruyama
Journal:  Arterioscler Thromb Vasc Biol       Date:  2003-03-06       Impact factor: 8.311

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  1 in total

1.  Sodium ferulate lowers portal pressure in rats with secondary biliary cirrhosis through the RhoA/Rho-kinase signaling pathway: a preliminary study.

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Journal:  Int J Mol Med       Date:  2014-08-19       Impact factor: 4.101

  1 in total

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