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Peripheral benzodiazepine receptor regulates vascular endothelial activations via suppression of the voltage-dependent anion channel-1

  作者 Joo, HK; Lee, YR; Lim, SY; Lee, EJ; Choi, S; Cho, EJ; Park, MS; Ryoo, S; Park, JB; Jeon, BH  
  选自 期刊  FEBS Letters;  卷期  2012年586-9;  页码  1349-1355  
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[摘要]Peripheral benzodiazepine receptor (PBR) is a multifunctional protein mainly found on the outer mitochondrial membrane. PBR expression is increased by tumor necrosis factor-alpha (TNF-alpha) in endothelial cells. Adenoviral overexpression of PBR inhibits monocyte adhesion, VCAM-1, and ICAM-1 expression in TNF-alpha-activated endothelial cells. Rotenone, cyclosporine A, and bongkrekic acid suppress TNF-alpha-induced VCAM-1 expression. Overexpression of PBR inhibits voltage-dependent anion channel-1 (VDAC-1) expression and the silencing of PBR increases VDAC-1 expression in endothelial cells. Moreover, TNF-alpha-induced VCAM-1 expression is suppressed by VDAC-1 gene silencing. PBR overexpression significantly decreases TNF-alpha-induced mitochondrial reactive oxygen species and MnSOD expression. These results suggest that PBR can inhibit endothelial activation and this action is related to the inhibition of mitochondrial ROS and/or VDAC-1 expression in endothelial cells. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

 
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