Compartmentalized nitric oxide signaling in the resistance vasculature

被引:32
作者
Mutchler, Stephanie M. [1 ]
Straub, Adam C. [1 ]
机构
[1] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15216 USA
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2015年 / 49卷
关键词
Nitric oxide; Resistance artery; Vascular tone; Myoendothelial junction; Hemoglobin; MYOENDOTHELIAL GAP-JUNCTIONS; PROTEIN S-NITROSYLATION; INDEPENDENT ENOS ACTIVATION; ENDOTHELIAL GROWTH-FACTOR; HYPERPOLARIZING FACTOR; SMOOTH-MUSCLE; MESENTERIC-ARTERIES; CONNEXIN EXPRESSION; POTASSIUM CHANNELS; HEMOGLOBIN ALPHA;
D O I
10.1016/j.niox.2015.05.003
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
Nitric oxide (NO) was first described as a bioactive molecule through its ability to stimulate soluble guanylate cyclase, but the revelation that NO was the endothelium derived relaxation factor drove the field to its modern state. The wealth of research conducted over the past 30 years has provided us with a picture of how diverse NO signaling can be within the vascular wall, going beyond simple vasodilation to include such roles as signaling through protein S-nitrosation. This expanded view of NO's actions requires highly regulated and compartmentalized production. Importantly, resistance arteries house multiple proteins involved in the production and transduction of NO allowing for efficient movement of the molecule to regulate vascular tone and reactivity. In this review, we focus on the many mechanisms regulating NO production and signaling action in the vascular wall, with a focus on the control of endothelial nitric oxide synthase (eNOS), the enzyme responsible for synthesizing most of the NO within these confines. We also explore how cross talk between the endothelium and smooth muscle in the microcirculation can modulate NO signaling, illustrating that this one small molecule has the capability to produce a plethora of responses. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:8 / 15
页数:8
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