Ceruloplasmin alters intracellular iron regulated proteins and pathways: Ferritin, transferrin receptor, glutamate and hypoxia-inducible factor-1α
| Autor: | J B Ferrell, Mary Christine McGahan, S. Nagar, Malgorzata Goralska, J. Harned, Lloyd N. Fleisher |
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| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: |
Glutamic Acid
Transferrin receptor Retinal Pigment Epithelium Iron Chelating Agents Article Cellular and Molecular Neuroscience Dogs Lens Crystalline Receptors Transferrin medicine Animals Aceruloplasminemia Fluorescent Antibody Technique Indirect Cells Cultured Oxalates biology Glutamate secretion Glutamate receptor Ceruloplasmin Epithelial Cells Glutamic acid medicine.disease Hypoxia-Inducible Factor 1 alpha Subunit Sensory Systems Cell biology Ferritin Ophthalmology Biochemistry Ferritins biology.protein Intracellular |
| Popis: | Ceruloplasmin (Cp) is a ferroxidase important to the regulation of both systemic and intracellular iron levels. Cp has a critical role in iron metabolism in the brain and retina as shown in patients with aceruloplasminemia and in Cp−/−hep−/y mice where iron accumulates and neural and retinal degeneration ensue. We have previously shown that cultured lens epithelial cells (LEC) secrete Cp. The purpose of the current study was to determine if cultured retinal pigmented epithelial cells (RPE) also secrete Cp. In addition, the effects of exogenously added Cp on iron regulated proteins and pathways, ferritin, transferrin receptor, glutamate secretion and levels of hypoxia-inducible factor-1α in the nucleus were determined. Like LEC, RPE secrete Cp. Cp was found diffusely distributed within both cultured LEC and RPE, but the cell membranes had more intense staining. Exogenously added Cp caused an increase in ferritin levels in both cell types and increased secretion of glutamate. The Cp-induced increase in glutamate secretion was inhibited by both the aconitase inhibitor oxalomalic acid as well as iron chelators. As predicted by the canonical view of the iron regulatory protein (IRP) as the predominant controller of cellular iron status these results indicate that there is an increase in available iron (called the labile iron pool (LIP)) in the cytoplasm. However, both transferrin receptor (TfR) and nuclear levels of HIF-1α were increased and these results point to a decrease in available iron. Such confounding results have been found in other systems and indicate that there is a much more complex regulation of intra-cellularly available iron (LIP) and its downstream effects on cell metabolism. Importantly, the Cp increased production and secretion of the neurotransmitter, glutamate, is a substantive finding of clinical relevance because of the neural and retinal degeneration found in aceruloplasminemia patients. This finding and Cp-induced nuclear translocation of the hypoxia-inducible factor-1 (HIF1) subunit HIF-1α adds novel information to the list of critical pathways impacted by Cp. |
| Databáze: | OpenAIRE |
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