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PMID: 10627630 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

NADPH oxidase contributes directly to oxidative stress and apoptosis in nerve growth factor-deprived sympathetic neurons.

Tammariello SP, Quinn MT, Estus S

Abstract

Reactive oxygen species (ROS) are necessary for programmed cell death (PCD) in neurons, but the underlying ROS-producing enzymes have not been identified. NADPH oxidase produces ROS, although the expression of its five subunits are thought to be restricted largely to non-neuronal cells. Here, we show that NADPH oxidase subunits are present in neurons. Moreover, both an NADPH oxidase inhibitor, diphenyleneiodonium, and NAPDH oxidase genetic deficiency inhibit apoptosis in a classic model of PCD, i.e., NGF-deprived sympathetic neurons. Overall, these results indicate that NADPH oxidase is unexpectedly present in neurons and can contribute to neuronal apoptosis.

MeSH Terms
Animals Apoptosis/physiology Cells, Cultured Enzyme Inhibitors/pharmacology Immunohistochemistry Mice NADPH Oxidases/antagonists & inhibitors,metabolism Nerve Growth Factor/deficiency,genetics Neurons/cytology,enzymology,metabolism Onium Compounds/pharmacology Oxidative Stress RNA, Messenger/metabolism Reactive Oxygen Species/metabolism Reverse Transcriptase Polymerase Chain Reaction Sympathetic Nervous System/cytology,enzymology,metabolism
Chemicals
Enzyme Inhibitors Onium Compounds RNA, Messenger Reactive Oxygen Species diphenyleneiodonium Nerve Growth Factor NADPH Oxidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tammariello S P
Department of Physiology, Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky 40536, USA.
Quinn M T
Estus S
Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
1529-2401
Published
2000-01-01
Pages
RC53
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6774145
Subset
IM
Grants
NIAMS NIH HHS · R01 AR-42426 · United States
NINDS NIH HHS · R29 NS-35607 · United States
NIA NIH HHS · T32AG-00242 · United States
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