TY - JOUR
T1 - Regulation of endothelium-derived nitric oxide production by the protein kinase Akt
AU - Fulton, David
AU - Gratton, Jean Philippe
AU - McCabe, Timothy J.
AU - Fontana, Jason
AU - Fujio, Yasushl
AU - Walsh, Kenneth
AU - Franke, Thomas F.
AU - Papapetropoulos, Andreas
AU - Sessa, William C.
PY - 1999/6/10
Y1 - 1999/6/10
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0033542414&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033542414&partnerID=8YFLogxK
U2 - 10.1038/21218
DO - 10.1038/21218
M3 - Article
C2 - 10376602
AN - SCOPUS:0033542414
SN - 0028-0836
VL - 399
SP - 597
EP - 601
JO - Nature
JF - Nature
IS - 6736
ER -