蛋白激酶B
伊诺斯
磷酸化
一氧化氮
细胞生物学
一氧化氮合酶Ⅲ型
一氧化氮合酶
化学
信号转导
生物
内分泌学
作者
David Fulton,Jean‐Philippe Gratton,Timothy J. McCabe,Jason Fontana,Yasushi Fujio,Kenneth Walsh,Thomas Franke,Andreas Papapetropoulos,William C. Sessa
出处
期刊:Nature
[Springer Nature]
日期:1999-06-10
卷期号:399 (6736): 597-601
被引量:2576
摘要
Endothelial nitric oxide synthase (eNOS) is the nitric oxide synthase isoform responsible for maintaining systemic blood pressure, vascular remodelling and angiogenesis. eNOS is phosphorylated in response to various forms of cellular stimulation, but the role of phosphorylation in the regulation of nitric oxide (NO) production and the kinase(s) responsible are not known. Here we show that the serine/threonine protein kinase Akt (protein kinase B) can directly phosphorylate eNOS on serine 1179 and activate the enzyme, leading to NO production, whereas mutant eNOS (S1179A) is resistant to phosphorylation and activation by Akt. Moreover, using adenovirus-mediated gene transfer, activated Akt increases basal NO release from endothelial cells, and activation-deficient Akt attenuates NO production stimulated by vascular endothelial growth factor. Thus, eNOS is a newly described Akt substrate linking signal transduction by Akt to the release of the gaseous second messenger NO.
科研通智能强力驱动
Strongly Powered by AbleSci AI