ICAM-1 cross-linking stimulates endothelial glutathione synthesis

被引:6
作者
Pruitt, Heather M.
Langston, Will
Kevil, Christopher G.
Patel, Rakesh P.
机构
[1] Univ Alabama, Dept Pathol, Mol & Celular Div, Birmingham, AL 35216 USA
[2] Univ Alabama, Ctr Free Radical Biol, Birmingham, AL 35216 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Dept Pathol, Shreveport, LA 71105 USA
关键词
D O I
10.1089/ars.2007.9.159
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
What mechanisms regulate endothelial glutathione (GSH) during inflammation? Addressing this question is critical in understanding mechanisms leading to endothelial dysfunction and cardiovascular disease. Herein, the authors show data that support the hypothesis that the intercellular cell adhesion molecule-1 (ICAM-1) regulates GSH. Ligating either constitutive or induced ICAM-1 on the endothelial surface, or exposing endothelial cells to soluble ICAM-1, increases GSH concentrations. ICAM-1 is important in mediating leukocyte adhesion and modulates endothelial signaling pathways important in controlling transmigration. The present data underscore a novel function for ICAM-1 in modulating GSH metabolism and raise the hypothesis that this adhesion molecule controls endothelial redox status under basal and inflammatory conditions.
引用
收藏
页码:159 / 164
页数:6
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