Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: EC:1.6.3.1 (
NADPH oxidase
)
11,281
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Endothelin (ET)-1 stimulates nicotinamide adenine dinucleotide phosphate (NADPH) oxidases and increases superoxide production in some cells such as vascular smooth muscle cells. Here, we reported that ET1 inhibited
NADPH oxidase
activity, superoxide generation, and cell proliferation in human abdominal aortic endothelial cells (HAAECs) via the
ETB1
-Pyk2-Rac1-Nox1 pathway. Superoxide production was determined by assessing ethidium fluorescence using flow cytometry in HAAECs exposed to ET1 (10-30 nm) at different time intervals. ET1 significantly decreased superoxide production in HAAECs in the presence of NG-nitro-L-arginine methyl ester, indicating that ET1 suppressed superoxide generation independent of nitric oxide synthase. ET1 significantly attenuated
NADPH oxidase
activity and cell proliferation, which could be abolished by silence of Nox1 gene, suggesting that ET1-induced inhibition of
NADPH oxidase
activity was mediated by Nox1. Furthermore, RNA interference silence of
ETB1
receptors significantly increased
NADPH oxidase
activity, and blocked the inhibitory effect of ET1 on
NADPH oxidase
activity. Activation of
ETB1
receptors by ET1 suppressed protein phosphorylation of pyk2 (Y402) and Rac1, suggesting that ET1 inhibited
NADPH oxidase
activity via
ETB1
-Pyk2-Rac1 pathway. Indeed, inhibition of Pyk2 by AG-17 abolished ET1-induced suppression of
NADPH oxidase
activity. ET1 also attenuated angiotensin II-induced activation of
NADPH oxidase
and cell proliferation. This study demonstrated, for the first time, that ET1, via
ETB1
, inhibited
NADPH oxidase
activity in HAAECs by suppressing the Pyk2-Rac1-Nox1 pathway. This finding reveals a novel function of
ETB1
receptors in regulating endothelial
NADPH oxidase
activity, superoxide production, and cell proliferation, opening a new avenue for understanding the role of
ETB1
receptors in protecting endothelial cells.
...
PMID:Endothelin (ET)-1 inhibits nicotinamide adenine dinucleotide phosphate oxidase activity in human abdominal aortic endothelial cells: a novel function of ETB1 receptors. 1853 8