Iron accentuated reactive oxygen species release by NADPH oxidase in activated microglia contributes to oxidative stress in vitro.
Yauger YJ1, Bermudez S2, Moritz KE1, Glaser E3, Stoica B3, Byrnes KR4,5.
J Neuroinflammation. 2019 Feb 18;16(1):41. doi: 10.1186/s12974-019-1430-7.

Abstract
BACKGROUND:
Excessive iron contributes to oxidative stress after central nervous system injury. NADPH oxidase (NOX) enzymes are upregulated in microglia after pro-inflammatory activation and contribute to oxidative stress. The relationship between iron, microglia,
NOX, and oxidative stress is currently unclear.

METHODS:
We evaluated the effects of iron on lipopolysaccharide (LPS)-activated microglia and its secondary effect within neuronal co-cultures. Further, NOX2 and four specific inhibitors were tested to evaluate the relationship with the reactive oxygen species (
ROS)-producing enzymes.

RESULTS:
An iron dose-dependent increase in ROS production among microglia treated with LPS was identified. Interestingly, despite this increase in ROS, inflammatory polarization alterations were not detected among the microglia after exposure to iron and LPS. Co-
culture experimentation between primary neurons and exposed microglia (iron and LPS) significantly reduced neuronal cell number at 24 h, suggesting a profound neurotoxic effect despite the lack of a change in polarization phenotype. NOX2 and NOX4
inhibition significantly reduced ROS production among microglia exposed to iron and LPS and reduced neuronal damage and death in response to microglial co-culture.

CONCLUSIONS:
In conclusion, iron significantly increased ROS production and neurotoxicity without exacerbating LP-activated microglia phenotype in vitro, suggesting that iron contributes to microglia-related oxidative stress, and this may be a viable therapeutic
target for injury or neurodegeneration. Further, this study highlights both NOX2 and NOX4 as potential therapeutic targets in the treatment of iron-induced microglia-related inflammation and neurotoxicity.

KEYWORDS:
BV2; Iron sulfate; Microglial polarization; Neuroinflammation; Neuronal toxicity

PMID: 30777083 PMCID: PMC6378754 DOI: 10.1186/s12974-019-1430-7

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