The eNOS signalosome and its link to endothelial dysfunction

被引:148
作者
Siragusa, Mauro [1 ]
Fleming, Ingrid [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Vasc Signalling, Ctr Mol Med, Theodor Stern Kai 7, D-60590 Frankfurt, Germany
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2016年 / 468卷 / 07期
关键词
Endothelium; Endothelial nitric oxide synthase; Signalosome; Uncoupling; Endothelial dysfunction; NITRIC-OXIDE SYNTHASE; CORONARY-ARTERY-DISEASE; CYCLOHYDROLASE-I OVEREXPRESSION; AKT-DEPENDENT PHOSPHORYLATION; RICH TYROSINE KINASE; FLUID SHEAR-STRESS; PROTEIN-KINASE; NO SYNTHASE; VASCULAR DYSFUNCTION; KNOCKOUT MICE;
D O I
10.1007/s00424-016-1839-0
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Endothelial nitric oxide synthase (eNOS) plays an essential role in the regulation of endothelial function and acts as a master regulator of vascular tone and homeostasis through the generation of the gasotransmitter nitric oxide (NO). The complex network of events mediating efficient NO synthesis is regulated by post-translational modifications and protein-protein interactions. Dysregulation of these mechanisms induces endothelial dysfunction, a term often used to refer to reduced NO bioavailability and consequent alterations in endothelial function, that are a hallmark of many cardiovascular diseases. Endothelial dysfunction is linked to eNOS uncoupling, which consists of a switch from the generation of NO to the generation of superoxide anions and hydrogen peroxide. This review provides an overview of the eNOS signalosome, integrating past and recently described protein-protein interactions that have been shown to play a role in the modulation of eNOS activity with implications for cardiovascular pathophysiology. The mechanisms underlying eNOS uncoupling and clinically relevant strategies that were adopted to influence them are also discussed.
引用
收藏
页码:1125 / 1137
页数:13
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