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Quiescence induced by iron challenge protects neuroblastoma cells from oxidative stress
Author(s) -
Mura Casilda V.,
Delgado Ricardo,
Aguirre Pabla,
Bacigalupo Juan,
Núñez Marco T.
Publication year - 2006
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2006.03798.x
Subject(s) - oxidative stress , substantia nigra , pars compacta , neurodegeneration , reactive oxygen species , population , microbiology and biotechnology , biology , oxidative phosphorylation , neuroblastoma , cell , chemistry , neuroscience , biochemistry , cell culture , medicine , genetics , dopamine , disease , dopaminergic , environmental health
Abstract The brain uses massive amounts of oxygen, generating large quantities of reactive oxygen species (ROS). Because of its lipid composition, rich in unsaturated fatty acids, the brain is especially vulnerable to ROS. Furthermore, oxidative damage in the brain is often associated with iron, which has pro‐oxidative properties. Iron‐mediated oxidative damage in the brain is compounded by the fact that brain iron distribution is non‐uniform, being particularly high in areas sensitive to neurodegeneration. This work was aimed to further our understanding of the cellular mechanisms by which SHSY5Y neuroblastoma cells adapt to, and survive increasing iron loads. Using an iron accumulation protocol that kills about 50% of the cell population, we found by cell sorting analysis that the SHSY5Y sub‐population that survived the iron loading arrested in the G 0 phase of the cell cycle. These cells expressed neuronal markers, while their electrical properties remained largely unaltered. These results suggest that upon iron challenge, neuroblastoma cells respond by entering the G 0 phase, somehow rendering them resistant to oxidative stress. A similar physiological condition might be involved in neuronal survival in tissues known to accumulate iron with age, such as the hippocampus and the substantia nigra pars compacta .

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