An oxidative stress-mediated positive-feedback iron uptake loop in neuronal cells
| Autor: | Claudia, Núñez-Millacura, Victoria, Tapia, Patricia, Muñoz, Ricardo B, Maccioni, Marco T, Núñez |
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| Rok vydání: | 2002 |
| Předmět: |
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Physiological Iron-Sulfur Proteins Neurons Time Factors Cell Survival Iron Deoxyguanosine Iron-Regulatory Proteins RNA-Binding Proteins DNA Antioxidants Acetylcysteine Cell Line Mice Neuroblastoma Oxidative Stress 8-Hydroxy-2'-Deoxyguanosine Animals Iron Regulatory Protein 1 Iron Regulatory Protein 2 Cells Cultured DNA Damage |
| Zdroj: | Journal of neurochemistry. 82(2) |
| ISSN: | 0022-3042 |
| Popis: | Intracellular reactive iron is a source of free radicals and a possible cause of cell damage. In this study, we analyzed the changes in iron homeostasis generated by iron accumulation in neuroblastoma (N2A) cells and hippocampal neurons. Increasing concentrations of iron in the culture medium elicited increasing amounts of intracellular iron and of the reactive iron pool. The cells had both IRP1 and IRP2 activities, being IRP1 activity quantitatively predominant. When iron in the culture medium increased from 1 to 40 microm, IRP2 activity decreased to nil. In contrast, IRP1 activity decreased when iron increased up to 20 microm, and then, unexpectedly, increased. IRP1 activity at iron concentrations above 20 microm was functional as it correlated with increased (55) Fe uptake. The increase in IRP1 activity was mediated by oxidative-stress as it was largely abolished by N-acetyl-L-cysteine. Culturing cells with iron resulted in proteins and DNA modifications. In summary, iron uptake by N2A cells and hippocampus neurons did not shut off at high iron concentrations in the culture media. As a consequence, iron accumulated and generated oxidative damage. This behavior is probably a consequence of the paradoxical activation of IRP1 at high iron concentrations, a condition that may underlie some processes associated with neuronal degeneration and death. |
| Databáze: | OpenAIRE |
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